<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">nefr</journal-id><journal-title-group><journal-title xml:lang="ru">Нефрология</journal-title><trans-title-group xml:lang="en"><trans-title>Nephrology (Saint-Petersburg)</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">1561-6274</issn><issn pub-type="epub">2541-9439</issn><publisher><publisher-name>Pavlov First Saint-Petersburg State Medical University</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">nefr-231</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ПЕРЕДОВАЯ СТАТЬЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>LEADING ARTICLE</subject></subj-group></article-categories><title-group><article-title>РЕГЕНЕРАТИВНЫЕ СТРАТЕГИИ РЕКОНСТРУИРОВАНИЯ ПОЧКИ</article-title><trans-title-group xml:lang="en"><trans-title>REGENERATIVE STRATEGIES FOR KIDNEY ENGINEERING</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Монтсеррат</surname><given-names>Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Montserrat</surname><given-names>N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Программы по плюрипотентным стволовым клеткам и активации эндогенной ткани для регенерации органов (PR Lab)</p></bio><bio xml:lang="en"><p>Pluripotent Stem Cells and Activation of Endogenous Tissue Programs for Organ Regeneration (PR Lab)</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гаррета</surname><given-names>Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Garreta</surname><given-names>E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Программы по плюрипотентным стволовым клеткам и активации эндогенной ткани для регенерации органов (PR Lab)</p></bio><bio xml:lang="en"><p>Pluripotent Stem Cells and Activation of Endogenous Tissue Programs for Organ Regeneration (PR Lab)</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бельмонте</surname><given-names>Х.К.И.</given-names></name><name name-style="western" xml:lang="en"><surname>Belmonte</surname><given-names>J.C.I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Лаборатория экспрессии гена</p></bio><bio xml:lang="en"><p>Gene Expression Laboratory</p></bio><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Институт Биоинжиниринга Каталонии (IBEC); &#13;
Сетевой биомедицинский исследовательский центр биоинжиниринга, биоматериалов и наномедицины (CIBER-BBN)</institution><country>Испания</country></aff><aff xml:lang="en"><institution>Institute for Bioengineering of Catalonia (IBEC); &#13;
Networking Biomedical Research Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Madrid</institution><country>Spain</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Институт Биоинжиниринга Каталонии (IBEC);</institution><country>Испания</country></aff><aff xml:lang="en"><institution>Institute for Bioengineering of Catalonia (IBEC)</institution><country>Spain</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Институт биологических исследований Солка</institution><country>Соединённые Штаты Америки</country></aff><aff xml:lang="en"><institution>Salk Institute for Biological Studies, La Jolla, CA</institution><country>United States</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2016</year></pub-date><pub-date pub-type="epub"><day>03</day><month>03</month><year>2017</year></pub-date><volume>20</volume><issue>6</issue><fpage>10</fpage><lpage>25</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Монтсеррат Н., Гаррета Е., Бельмонте Х., 2017</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="ru">Монтсеррат Н., Гаррета Е., Бельмонте Х.</copyright-holder><copyright-holder xml:lang="en">Montserrat N., Garreta E., Belmonte J.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://journal.nephrolog.ru/jour/article/view/231">https://journal.nephrolog.ru/jour/article/view/231</self-uri><abstract><p>Почка является важнейшим органом водного гомеостаза и экскреции токсических субстанций. Она выполняет несколько важных физиологических функций для обеспечения гомеостаза: удаляет циркулирующие продукты метаболизма, регулирует баланс жидкости в организме и действует как иммунный регулятор, а также модулятор нормального функционирования сердечно-сосудистой системы. В самое последнее время появились и активно развиваются модели почечных заболеваний in vitro с плюрипотентными стволовыми клетками (как стволовыми клетками человеческого эмбриона, так и индуцированными плюрипотентными стволовыми клетками), а также разрабатываются надежные протоколы по получению in vitro клеток, подобных специфичным ренальным, из индуцированных плюрипотентных стволовых клеток пациента. В данном обзоре мы приводим главные открытия в области регенерации почки с основным фокусом на развитие пошаговых протоколов по созданию почечных клеток из человеческих плюрипотентных стволовых клеток и самые последние достижения в области биоинжиниринга почки (т.е. децеллюляризированного почечного остова и биопринтинга). Возможность создания трехмерной структуры, подобной почке, с последующим наполнением ее индуцированными плюрипотентными стволовыми клетками почечного происхождения может открыть новые перспективы для создания функционирующего по требованию почечного трансплантата.</p><p>Статья переведена на русский язык и опубликована согласно условиям лицензии Creative Commons. Журнал FEBS J. 2016 Sep;283(18):3303–24. doi: 10.1111/febs.13704. Перевод М.С.Храбровой. Редакция перевода И.И.Трофименко</p></abstract><trans-abstract xml:lang="en"><p>The kidney is the most important organ for water homeostasis and waste excretion. It performs several important physiological functions for homeostasis: it filters the metabolic waste out of circulation, regulates body fluid balances, and acts as an immune regulator and modulator of cardiovascular physiology. The development of in vitro renal disease models with pluripotent stem cells (both human embryonic stem cells and induced pluripotent stem cells) and the generation of robust protocols for in vitro derivation of renal-specific-like cells from patient induced pluripotent stem cells have just emerged. Here we review major findings in the field of kidney regeneration with a major focus on the development of stepwise protocols for kidney cell production from human pluripotent stem cells and the latest advances in kidney bioengineering (i.e. decellularized kidney scaffolds and bioprinting). The possibility of generating renal-like three-dimensional structures to be recellularized with renal-derived induced pluripotent stem cells may offer new avenues to develop functional kidney grafts on-demand.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>индуцированные плюрипотентные стволовые клетки</kwd><kwd>заболевания почек</kwd><kwd>реконструкция почек</kwd><kwd>плюрипотентные стволовые клетки</kwd><kwd>почечно-клеточная дифференциация</kwd></kwd-group><kwd-group xml:lang="en"><kwd>induced pluripotent stem cells</kwd><kwd>kidney disease</kwd><kwd>kidney engineering</kwd><kwd>pluripotent stem cells</kwd><kwd>renal differentiation</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">M. Schwarz, P. Schwarz за административную помощь. N.M. был частично поддержан StG-2014-640525_REGMAMKID, RyC 2014-16242, Fundaci_o Privada La Marat_o de TV3 (121430/31/32) Министерством экономики и конкурентноспособности Испании (SAF2014-59778) и комиссией по университетам и научным исследованиям отдела инноваций, университетов и предприятий генералитата Каталонии (2014 SGR 1442). E.G. был частично поддержан StG-2014-640525_REGMAMKID and La Fundaci_o Privada La Marat_o de TV3, 121430/31/32. J.C.I.B. был поддержан грантами фонда Glenn, благотворительного фонда G.Harold и Leila Y.Mathers и благотворительный фонд.Leona M. and Harry B. Helmsley</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">https://www.kidney.org/news/newsroom/factsheets/Organ-Donation-and-Transplantation-Stats.</mixed-citation><mixed-citation xml:lang="en">https://www.kidney.org/news/newsroom/factsheets/Organ-Donation-and-Transplantation-Stats.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">http://optn.transplant.hrsa.gov/3. Song B, Smink AM, Jones CV, et al. The directed differentiation of human iPS cell into kidney podocytes. PLoS One 2012; 7, e46453</mixed-citation><mixed-citation xml:lang="en">http://optn.transplant.hrsa.gov/3. Song B, Smink AM, Jones CV, et al. The directed differentiation of human iPS cell into kidney podocytes. PLoS One 2012; 7, e46453</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Narayanan K, Schumacher KM, Tasnim F et al. Human embryonic stem cells differentiate into functional renal proximal tubular-like cells. Kidney 2013; Int 83, 593–603</mixed-citation><mixed-citation xml:lang="en">Narayanan K, Schumacher KM, Tasnim F et al. Human embryonic stem cells differentiate into functional renal proximal tubular-like cells. Kidney 2013; Int 83, 593–603</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Кatari R, Peloso A, Zambon JP et al. Renal bioengineering with scaffolds generated from human kidneys. Nephron 2014; Exp Nephrol 126, 119–124</mixed-citation><mixed-citation xml:lang="en">Кatari R, Peloso A, Zambon JP et al. Renal bioengineering with scaffolds generated from human kidneys. Nephron 2014; Exp Nephrol 126, 119–124</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Mandrycky C, Wang Z, Kim K &amp; Kim DH. 3D bioprinting for engineering complex tissues. Biotechnol 2015; Adv doi: 10.1016/j. biotechadv.2015.12.011</mixed-citation><mixed-citation xml:lang="en">Mandrycky C, Wang Z, Kim K &amp; Kim DH. 3D bioprinting for engineering complex tissues. Biotechnol 2015; Adv doi: 10.1016/j. biotechadv.2015.12.011</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Montserrat N, Ramırez-Bajo MJ, Xia Y et al. Generation of induced pluripotent stem cells from human renal proximal tubular cells with only two transcription factors, OCT4 and SOX2. J Biol Chem 2012; 287, 24131–24138</mixed-citation><mixed-citation xml:lang="en">Montserrat N, Ramırez-Bajo MJ, Xia Y et al. Generation of induced pluripotent stem cells from human renal proximal tubular cells with only two transcription factors, OCT4 and SOX2. J Biol Chem 2012; 287, 24131–24138</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Baer PC, Geiger H. Human renal cells from the thick ascending limb and early distal tubule: characterization of primary isolated and cultured cells by reverse transcription polymerase chain reaction. Nephrology 2008; 13, 316–321</mixed-citation><mixed-citation xml:lang="en">Baer PC, Geiger H. Human renal cells from the thick ascending limb and early distal tubule: characterization of primary isolated and cultured cells by reverse transcription polymerase chain reaction. Nephrology 2008; 13, 316–321</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Baer PC, Nockher WA, Haase W, Scherberich JE. Isolation of proximal and distal tubule cells from human kidney by immunomagnetic separation. Technical note. Kidney 1997; Int 52, 1321–1331</mixed-citation><mixed-citation xml:lang="en">Baer PC, Nockher WA, Haase W, Scherberich JE. Isolation of proximal and distal tubule cells from human kidney by immunomagnetic separation. Technical note. Kidney 1997; Int 52, 1321–1331</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Humphreys BD, Czerniak S, DiRocco DP, et al. Repair of injured proximal tubule does not involve specialized progenitors. Proc Natl Acad Sci USA 2011; 108, 9226-9231</mixed-citation><mixed-citation xml:lang="en">Humphreys BD, Czerniak S, DiRocco DP, et al. Repair of injured proximal tubule does not involve specialized progenitors. Proc Natl Acad Sci USA 2011; 108, 9226-9231</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Song J, Czerniak S, Wang T et al. Characterization and fate of telomerase-expressing epithelia during kidney repair. J Am Soc Nephrol 2011; 22, 2256–2265</mixed-citation><mixed-citation xml:lang="en">Song J, Czerniak S, Wang T et al. Characterization and fate of telomerase-expressing epithelia during kidney repair. J Am Soc Nephrol 2011; 22, 2256–2265</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Humphreys BD, Valerius MT, Kobayashi A et al. Intrinsic epithelial cells repair the kidney after injury. Cell Stem Cell 2008; 2, 284–291</mixed-citation><mixed-citation xml:lang="en">Humphreys BD, Valerius MT, Kobayashi A et al. Intrinsic epithelial cells repair the kidney after injury. Cell Stem Cell 2008; 2, 284–291</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Romagnani P, Lasagni L, Remuzzi G. Renal progenitors: an evolutionary conserved strategy for kidney regeneration. Nat Rev Nephrol 2013; 9, 137–146</mixed-citation><mixed-citation xml:lang="en">Romagnani P, Lasagni L, Remuzzi G. Renal progenitors: an evolutionary conserved strategy for kidney regeneration. Nat Rev Nephrol 2013; 9, 137–146</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Romagnani P, Anders H-J. What can tubular progenitor cultures teach us about kidney regeneration? Kidney 2013; Int 83, 351–353</mixed-citation><mixed-citation xml:lang="en">Romagnani P, Anders H-J. What can tubular progenitor cultures teach us about kidney regeneration? Kidney 2013; Int 83, 351–353</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Osafune K, Takasato M, Kispert A, Asashima MNR. Identification of multipotent progenitors in the embryonic mouse kidney by a novel colonyforming assay. Development 2006; 133, 151–161</mixed-citation><mixed-citation xml:lang="en">Osafune K, Takasato M, Kispert A, Asashima MNR. Identification of multipotent progenitors in the embryonic mouse kidney by a novel colonyforming assay. Development 2006; 133, 151–161</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Little MH, McMahon AP. Mammalian kidney development: principles, progress, and projections.Cold Spring Harb Perspect Biol 2012; 4, 3</mixed-citation><mixed-citation xml:lang="en">Little MH, McMahon AP. Mammalian kidney development: principles, progress, and projections.Cold Spring Harb Perspect Biol 2012; 4, 3</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Thomson JA. Embryonic stem cell lines derived from human blastocysts. Science 1998; 282, 1145–1147</mixed-citation><mixed-citation xml:lang="en">Thomson JA. Embryonic stem cell lines derived from human blastocysts. Science 1998; 282, 1145–1147</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Wakayama T, Tabar V, Rodriguez I et al. Differentiation of embryonic stem cell lines generated from adult somatic cells by nuclear transfer. Science 2001; 292, 740–743</mixed-citation><mixed-citation xml:lang="en">Wakayama T, Tabar V, Rodriguez I et al. Differentiation of embryonic stem cell lines generated from adult somatic cells by nuclear transfer. Science 2001; 292, 740–743</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Tada M, Takahama Y, Abe K et al. Nuclear reprogramming of somatic cells by in vitro hybridization with ES cells. Curr Biol 2001; 11, 1553–1558</mixed-citation><mixed-citation xml:lang="en">Tada M, Takahama Y, Abe K et al. Nuclear reprogramming of somatic cells by in vitro hybridization with ES cells. Curr Biol 2001; 11, 1553–1558</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Hou P, Li Y, Zhang X et al. Pluripotent stem cells induced from mouse somatic cells by smallmolecule compounds. Science 2013; 341, 651–654</mixed-citation><mixed-citation xml:lang="en">Hou P, Li Y, Zhang X et al. Pluripotent stem cells induced from mouse somatic cells by smallmolecule compounds. Science 2013; 341, 651–654</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Takahashi K, Tanabe K, Ohnuki M et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell 2007; 131, 861–872</mixed-citation><mixed-citation xml:lang="en">Takahashi K, Tanabe K, Ohnuki M et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell 2007; 131, 861–872</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Kazutoshi Takahashi SY. A developmental framework for induced pluripotency. Development 2015; 142,3274–3285</mixed-citation><mixed-citation xml:lang="en">Kazutoshi Takahashi SY. A developmental framework for induced pluripotency. Development 2015; 142,3274–3285</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">.Zhu S, Li W, Zhou H, Wei et al. Reprogramming of human primary somatic cells by OCT4 and chemical compounds. Cell Stem Cell 2010; 7, 651–655</mixed-citation><mixed-citation xml:lang="en">.Zhu S, Li W, Zhou H, Wei et al. Reprogramming of human primary somatic cells by OCT4 and chemical compounds. Cell Stem Cell 2010; 7, 651–655</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Aasen T, Raya A, Barrero MJ et al. Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes. Nat Biotechnol 2008; 26, 1276–1284</mixed-citation><mixed-citation xml:lang="en">Aasen T, Raya A, Barrero MJ et al. Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes. Nat Biotechnol 2008; 26, 1276–1284</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Giorgetti A, Montserrat N, Aasen T et al. Generation of induced pluripotent stem cells from human cord blood using OCT4 and SOX2. Cell Stem Cell 2009; 5, 353–357</mixed-citation><mixed-citation xml:lang="en">Giorgetti A, Montserrat N, Aasen T et al. Generation of induced pluripotent stem cells from human cord blood using OCT4 and SOX2. Cell Stem Cell 2009; 5, 353–357</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Kim JB, Greber B, Ara et al. Direct reprogramming of human neural stem cells by OCT4. Nature 2009; 461, 649–643</mixed-citation><mixed-citation xml:lang="en">Kim JB, Greber B, Ara et al. Direct reprogramming of human neural stem cells by OCT4. Nature 2009; 461, 649–643</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Gonzalez F, Boue S, Belmonte JCI. Methods for making induced pluripotent stem cells: reprogramming a la carte. Nat Rev Genet 2011; 12, 231–242</mixed-citation><mixed-citation xml:lang="en">Gonzalez F, Boue S, Belmonte JCI. Methods for making induced pluripotent stem cells: reprogramming a la carte. Nat Rev Genet 2011; 12, 231–242</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou H, Wu S, Joo JY et al. Generation of induced pluripotent stem cells using recombinant proteins. Cell Stem Cell 2009; 4, 381–384</mixed-citation><mixed-citation xml:lang="en">Zhou H, Wu S, Joo JY et al. Generation of induced pluripotent stem cells using recombinant proteins. Cell Stem Cell 2009; 4, 381–384</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Kim D, Kim C-H, Moon J-I et al. Generation of human induced pluripotent stem cells by direct delivery of reprogramming proteins. Cell Stem Cell 2009; 4, 472–476</mixed-citation><mixed-citation xml:lang="en">Kim D, Kim C-H, Moon J-I et al. Generation of human induced pluripotent stem cells by direct delivery of reprogramming proteins. Cell Stem Cell 2009; 4, 472–476</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Okita K, Matsumura Y, Sato Y et al. A more efficient method to generate integration-free human iPS cells. Nat Methods 2011; 8, 409–412</mixed-citation><mixed-citation xml:lang="en">Okita K, Matsumura Y, Sato Y et al. A more efficient method to generate integration-free human iPS cells. Nat Methods 2011; 8, 409–412</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Warren L, Manos PD, Ahfeldt T et al. Highly efficient reprogramming to pluripotency and directed differentiation of human cells with synthetic modified mRNA. Cell Stem Cell 2010; 7, 618–630</mixed-citation><mixed-citation xml:lang="en">Warren L, Manos PD, Ahfeldt T et al. Highly efficient reprogramming to pluripotency and directed differentiation of human cells with synthetic modified mRNA. Cell Stem Cell 2010; 7, 618–630</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Anokye-Danso F, Trivedi CM, Juhr D et al. Highly efficient miRNA-mediated reprogramming of mouse and human somatic cells to pluripotency. Cell Stem Cell 2011; 8, 376–388</mixed-citation><mixed-citation xml:lang="en">Anokye-Danso F, Trivedi CM, Juhr D et al. Highly efficient miRNA-mediated reprogramming of mouse and human somatic cells to pluripotency. Cell Stem Cell 2011; 8, 376–388</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Meng G, Liu S, Rancourt DE. Synergistic effect of medium, matrix, and exogenous factors on the adhesion and growth of human pluripotent stem cells under defined, xeno-free conditions. Stem Cells Dev 2012; 21, 2036–2048</mixed-citation><mixed-citation xml:lang="en">Meng G, Liu S, Rancourt DE. Synergistic effect of medium, matrix, and exogenous factors on the adhesion and growth of human pluripotent stem cells under defined, xeno-free conditions. Stem Cells Dev 2012; 21, 2036–2048</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Sugii S, Kida Y, Kawamura T et al. Human and mouse adiposederived cells support feeder-independent induction of pluripotent stem cells. Proc Natl Acad Sci USA 2010; 107, 3558–3563.</mixed-citation><mixed-citation xml:lang="en">Sugii S, Kida Y, Kawamura T et al. Human and mouse adiposederived cells support feeder-independent induction of pluripotent stem cells. Proc Natl Acad Sci USA 2010; 107, 3558–3563.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Nakagawa M, Taniguchi Y, Senda S et al. A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells. Sci Rep 2014; 4, 3594</mixed-citation><mixed-citation xml:lang="en">Nakagawa M, Taniguchi Y, Senda S et al. A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells. Sci Rep 2014; 4, 3594</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Raya A, Rodrıguez-Piza I, Guenechea G et al. Diseasecorrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells. Nature 2009; 460, 53–59</mixed-citation><mixed-citation xml:lang="en">Raya A, Rodrıguez-Piza I, Guenechea G et al. Diseasecorrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells. Nature 2009; 460, 53–59</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Ebert AD, Yu J, Rose FF et al. Induced pluripotent stem cells from a spinal muscular atrophy patient. Nature 2009; 457, 277–280</mixed-citation><mixed-citation xml:lang="en">Ebert AD, Yu J, Rose FF et al. Induced pluripotent stem cells from a spinal muscular atrophy patient. Nature 2009; 457, 277–280</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Ye L, Chang JC, Lin C et al. Induced pluripotent stem cells offer new approach to therapy in thalassemia and sickle cell anemia and option in prenatal diagnosis in genetic diseases. Proc Natl Acad Sci USA 2009; 106, 9826–9830</mixed-citation><mixed-citation xml:lang="en">Ye L, Chang JC, Lin C et al. Induced pluripotent stem cells offer new approach to therapy in thalassemia and sickle cell anemia and option in prenatal diagnosis in genetic diseases. Proc Natl Acad Sci USA 2009; 106, 9826–9830</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Liu G-H, Barkho BZ, Ruiz S et al. Recapitulation of premature aging with iPSCs from Hutchinson-Gilford progeria syndrome. Nature 2009; 472, 221–225</mixed-citation><mixed-citation xml:lang="en">Liu G-H, Barkho BZ, Ruiz S et al. Recapitulation of premature aging with iPSCs from Hutchinson-Gilford progeria syndrome. Nature 2009; 472, 221–225</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Itzhaki I, Maizels L, Huber I et al. Modelling the long QT syndrome with induced pluripotent stem cells. Nature 2011; 471, 225–229</mixed-citation><mixed-citation xml:lang="en">Itzhaki I, Maizels L, Huber I et al. Modelling the long QT syndrome with induced pluripotent stem cells. Nature 2011; 471, 225–229</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Nguyen HN, Byers B, Cord B et al. LRRK2 mutant iPSCderived DA neurons demonstrate increased susceptibility to oxidative stress. Cell Stem Cell 2011; 8, 267–280</mixed-citation><mixed-citation xml:lang="en">Nguyen HN, Byers B, Cord B et al. LRRK2 mutant iPSCderived DA neurons demonstrate increased susceptibility to oxidative stress. Cell Stem Cell 2011; 8, 267–280</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Lee G, Papapetrou EP, Kim H et al. Modeling pathogenesis and treatment of familial dysautonomia using patient specific iPSCs. Nature 2011; 461, 402–406</mixed-citation><mixed-citation xml:lang="en">Lee G, Papapetrou EP, Kim H et al. Modeling pathogenesis and treatment of familial dysautonomia using patient specific iPSCs. Nature 2011; 461, 402–406</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Moretti A, Bellin M, Welling A et al. Patient-specific induced pluripotent stem-cell models for long-QT syndrome. N Engl J Med 2010; 363, 1397–1409</mixed-citation><mixed-citation xml:lang="en">Moretti A, Bellin M, Welling A et al. Patient-specific induced pluripotent stem-cell models for long-QT syndrome. N Engl J Med 2010; 363, 1397–1409</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Li M, Suzuki K, Kim NY et al. A cut above the rest: targeted genome editing technologies in human pluripotent stem cells. J Biol Chem 2014; 289, 4594–4599</mixed-citation><mixed-citation xml:lang="en">Li M, Suzuki K, Kim NY et al. A cut above the rest: targeted genome editing technologies in human pluripotent stem cells. J Biol Chem 2014; 289, 4594–4599</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Liu G-H, Suzuki K, Qu J et al. Targeted gene correction of laminopathyassociated LMNA mutations in patient-specific iPSCs. Cell Stem Cell 2011; 8, 688–694</mixed-citation><mixed-citation xml:lang="en">Liu G-H, Suzuki K, Qu J et al. Targeted gene correction of laminopathyassociated LMNA mutations in patient-specific iPSCs. Cell Stem Cell 2011; 8, 688–694</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Howden SE, Gore A, Li Z et al. Genetic correction and analysis of induced pluripotent stem cells from a patient with gyrate atrophy. Proc Natl Acad Sci USA 2011; 108, 6537–6542</mixed-citation><mixed-citation xml:lang="en">Howden SE, Gore A, Li Z et al. Genetic correction and analysis of induced pluripotent stem cells from a patient with gyrate atrophy. Proc Natl Acad Sci USA 2011; 108, 6537–6542</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Papapetrou EP, Lee G, Malani N et al. Genomic safe harbors permit high b-globin transgene expression in thalassemia induced pluripotent stem cells. Nat Biotechnol 2011; 29,73–78</mixed-citation><mixed-citation xml:lang="en">Papapetrou EP, Lee G, Malani N et al. Genomic safe harbors permit high b-globin transgene expression in thalassemia induced pluripotent stem cells. Nat Biotechnol 2011; 29,73–78</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Li M, Suzuki K, Qu J et al. Efficient correction of hemoglobinopathycausing mutations by homologous recombination in integration-free patient iPSCs. Cell Res 2011; 21, 1740–1744</mixed-citation><mixed-citation xml:lang="en">Li M, Suzuki K, Qu J et al. Efficient correction of hemoglobinopathycausing mutations by homologous recombination in integration-free patient iPSCs. Cell Res 2011; 21, 1740–1744</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Liu G-H, Qu J, Suzuki K et al. Progressive degeneration of human neural stem cells caused by pathogenic LRRK2. Nature 2012; 491, 603–607</mixed-citation><mixed-citation xml:lang="en">Liu G-H, Qu J, Suzuki K et al. Progressive degeneration of human neural stem cells caused by pathogenic LRRK2. Nature 2012; 491, 603–607</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Fattahi F, Steinbeck JA, Kriks S et al. Deriving human ENS lineages for cell therapy and drug discovery in Hirschsprung disease. Nature 2016; 531, 105–109</mixed-citation><mixed-citation xml:lang="en">Fattahi F, Steinbeck JA, Kriks S et al. Deriving human ENS lineages for cell therapy and drug discovery in Hirschsprung disease. Nature 2016; 531, 105–109</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Tiscornia G, Vivas EL, Izpisua Belmonte JC. Diseases in a dish: modeling human genetic disorders using induced pluripotent cells. Nat Med 2011; 17, 1570–1576</mixed-citation><mixed-citation xml:lang="en">Tiscornia G, Vivas EL, Izpisua Belmonte JC. Diseases in a dish: modeling human genetic disorders using induced pluripotent cells. Nat Med 2011; 17, 1570–1576</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Shankland SJ, Pippin JW, Reiser J, Mundel P. Podocytes in culture: past, present, and future. Kidney Int 2007; 72, 26–36</mixed-citation><mixed-citation xml:lang="en">Shankland SJ, Pippin JW, Reiser J, Mundel P. Podocytes in culture: past, present, and future. Kidney Int 2007; 72, 26–36</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Mae S-I, Shono A, Shiota F et al. Monitoring and robust induction of nephrogenic intermediate mesoderm from human pluripotent stem cells. Nat Commun 2013; 4, 1367</mixed-citation><mixed-citation xml:lang="en">Mae S-I, Shono A, Shiota F et al. Monitoring and robust induction of nephrogenic intermediate mesoderm from human pluripotent stem cells. Nat Commun 2013; 4, 1367</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Araoka T, Mae S, Kurose Y et al. Efficient and rapid induction of human iPSCs/ESCs into nephrogenic intermediate mesoderm using small molecule-based differentiation methods. PLoS One 2014; 9, e84881</mixed-citation><mixed-citation xml:lang="en">Araoka T, Mae S, Kurose Y et al. Efficient and rapid induction of human iPSCs/ESCs into nephrogenic intermediate mesoderm using small molecule-based differentiation methods. PLoS One 2014; 9, e84881</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Xia Y, Nivet E, Sancho-Martinez I et al. Directed differentiation of human pluripotent cells to ureteric bud kidney progenitorlike cells. Nat Cell Biol 2013; 15, 1507–1515</mixed-citation><mixed-citation xml:lang="en">Xia Y, Nivet E, Sancho-Martinez I et al. Directed differentiation of human pluripotent cells to ureteric bud kidney progenitorlike cells. Nat Cell Biol 2013; 15, 1507–1515</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Takasato M, Er PX, Becroft M et al. Directing human embryonic stem cell differentiation towards a renal lineage generates a self-organizing kidney. Nat Cell Biol 2014; 16, 118–126</mixed-citation><mixed-citation xml:lang="en">Takasato M, Er PX, Becroft M et al. Directing human embryonic stem cell differentiation towards a renal lineage generates a self-organizing kidney. Nat Cell Biol 2014; 16, 118–126</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Lam AQ, Freedman BS, Morizane R et al. Rapid and efficient differentiation of human pluripotent stem cells into intermediate mesoderm that forms tubules expressing kidney proximal tubular markers. J Am Soc Nephrol 2013; 25, 1211–1225</mixed-citation><mixed-citation xml:lang="en">Lam AQ, Freedman BS, Morizane R et al. Rapid and efficient differentiation of human pluripotent stem cells into intermediate mesoderm that forms tubules expressing kidney proximal tubular markers. J Am Soc Nephrol 2013; 25, 1211–1225</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Taguchi A, Kaku Y, Ohmori T et al. Redefining the in vivo origin of metanephric nephron progenitors enables generation of complex kidney structures from pluripotent stem cells. Cell Stem Cell 2014; 14, 53–67</mixed-citation><mixed-citation xml:lang="en">Taguchi A, Kaku Y, Ohmori T et al. Redefining the in vivo origin of metanephric nephron progenitors enables generation of complex kidney structures from pluripotent stem cells. Cell Stem Cell 2014; 14, 53–67</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Imberti B, Tomasoni S, Ciampi O et al. Renal progenitors derived from human iPSCs engraft and restore function in a mouse model of acute kidney injury. Sci Rep 2015; 5, 8826</mixed-citation><mixed-citation xml:lang="en">Imberti B, Tomasoni S, Ciampi O et al. Renal progenitors derived from human iPSCs engraft and restore function in a mouse model of acute kidney injury. Sci Rep 2015; 5, 8826</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Morizane R, Lam AQ, Freedman BS et al. Nephron organoids derived from human pluripotent stem cells model kidney development and injury. Nat Biotechnol 2015; 33, 1193–1200</mixed-citation><mixed-citation xml:lang="en">Morizane R, Lam AQ, Freedman BS et al. Nephron organoids derived from human pluripotent stem cells model kidney development and injury. Nat Biotechnol 2015; 33, 1193–1200</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Freedman BS, Brooks CR, Lam AQ et al. Modelling kidney disease with CRISPR-mutant kidney organoids derived from human pluripotent epiblast spheroids. Nat Commun 2015; 6, 8715</mixed-citation><mixed-citation xml:lang="en">Freedman BS, Brooks CR, Lam AQ et al. Modelling kidney disease with CRISPR-mutant kidney organoids derived from human pluripotent epiblast spheroids. Nat Commun 2015; 6, 8715</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Takasato M, Er PX, Chiu HS et al. Kidney organoids from human iPS cells contain multiple lineages and model human nephrogenesis. Nature 2015; 526, 564–568</mixed-citation><mixed-citation xml:lang="en">Takasato M, Er PX, Chiu HS et al. Kidney organoids from human iPS cells contain multiple lineages and model human nephrogenesis. Nature 2015; 526, 564–568</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Xiao-Jie L, Hui-Ying X, Zun-Ping K et al. CRISPR-Cas9: a new and promising player in gene therapy. J Med Genet 2015; 52, 289–296</mixed-citation><mixed-citation xml:lang="en">Xiao-Jie L, Hui-Ying X, Zun-Ping K et al. CRISPR-Cas9: a new and promising player in gene therapy. J Med Genet 2015; 52, 289–296</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Hu J, Lei Y, Wong W-K, Liu S et al. Direct activation of human and mouse Oct4 genes using engineered TALE and Cas9 transcription factors. Nucleic Acids Res 2014; 42, 4375–4390</mixed-citation><mixed-citation xml:lang="en">Hu J, Lei Y, Wong W-K, Liu S et al. Direct activation of human and mouse Oct4 genes using engineered TALE and Cas9 transcription factors. Nucleic Acids Res 2014; 42, 4375–4390</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Elliott DA, Braam SR, Koutsis K et al. NKX2-5eGFP/w hESCs for isolation of human cardiac progenitors and cardiomyocytes. Nat Methods 2011; 8, 1037–1040</mixed-citation><mixed-citation xml:lang="en">Elliott DA, Braam SR, Koutsis K et al. NKX2-5eGFP/w hESCs for isolation of human cardiac progenitors and cardiomyocytes. Nat Methods 2011; 8, 1037–1040</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Den Hartogh SC, Schreurs C, Monshouwer-Kloots JJ et al. Dual reporter MESP1 mCherry/w -NKX2-5 eGFP/w hESCs enable studying early human cardiac differentiation. Stem Cells 2015; 33, 56–67</mixed-citation><mixed-citation xml:lang="en">Den Hartogh SC, Schreurs C, Monshouwer-Kloots JJ et al. Dual reporter MESP1 mCherry/w -NKX2-5 eGFP/w hESCs enable studying early human cardiac differentiation. Stem Cells 2015; 33, 56–67</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Krentz NA, Nian CLF. TALEN/CRISPRmediated eGFP knock-in add-on at the OCT4 locus does not impact differentiation of human embryonic stem cells towards endoderm. PLoS One 2014; 9, e114275</mixed-citation><mixed-citation xml:lang="en">Krentz NA, Nian CLF. TALEN/CRISPRmediated eGFP knock-in add-on at the OCT4 locus does not impact differentiation of human embryonic stem cells towards endoderm. PLoS One 2014; 9, e114275</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Langer R, Vacanti JP. Tissue engineering. Science 1993; 260, 920–926 69. Kim TG, Shin H, Lim DW. Biomimetic scaffolds for tissue engineering. Adv Funct Mater 2012; 22, 2446–2468</mixed-citation><mixed-citation xml:lang="en">Langer R, Vacanti JP. Tissue engineering. Science 1993; 260, 920–926 69. Kim TG, Shin H, Lim DW. Biomimetic scaffolds for tissue engineering. Adv Funct Mater 2012; 22, 2446–2468</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Mallick KK, Cox SC. Biomaterial scaffolds for tissue engineering. Front Biosci 2013; 5, 341–360</mixed-citation><mixed-citation xml:lang="en">Mallick KK, Cox SC. Biomaterial scaffolds for tissue engineering. Front Biosci 2013; 5, 341–360</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Kamel RA, Ong JF, Eriksson E et al. Tissue engineering of skin. J Am Coll Surg 2013; 217: 533–555</mixed-citation><mixed-citation xml:lang="en">Kamel RA, Ong JF, Eriksson E et al. Tissue engineering of skin. J Am Coll Surg 2013; 217: 533–555</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Sittinger M, Bujia J, Minuth WW et al. Engineering of cartilage tissue using bioresorbable polymer carriers in perfusion culture. Biomaterials 1994; 15, 451–456</mixed-citation><mixed-citation xml:lang="en">Sittinger M, Bujia J, Minuth WW et al. Engineering of cartilage tissue using bioresorbable polymer carriers in perfusion culture. Biomaterials 1994; 15, 451–456</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Liao J, Guo X, Grande-Allen KJ et al. Bioactive polymer/ extracellular matrix scaffolds fabricated with a flow perfusion bioreactor for cartilage tissue engineering. Biomaterials 2010; 31, 8911–8920</mixed-citation><mixed-citation xml:lang="en">Liao J, Guo X, Grande-Allen KJ et al. Bioactive polymer/ extracellular matrix scaffolds fabricated with a flow perfusion bioreactor for cartilage tissue engineering. Biomaterials 2010; 31, 8911–8920</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Amini AR, Laurencin CT, Nukavarapu SP. Bone tissue engineering: recent advances and challenges. Crit Rev Biomed Eng 2012; 40, 363–408</mixed-citation><mixed-citation xml:lang="en">Amini AR, Laurencin CT, Nukavarapu SP. Bone tissue engineering: recent advances and challenges. Crit Rev Biomed Eng 2012; 40, 363–408</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Atala A. Tissue engineering of human bladder. Br Med Bull 2011; 97, 81–104</mixed-citation><mixed-citation xml:lang="en">Atala A. Tissue engineering of human bladder. Br Med Bull 2011; 97, 81–104</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Koike N, Fukumura D, Gralla O et al. Tissue engineering: creation of longlasting blood vessels. Nature 2004; 428, 138–139</mixed-citation><mixed-citation xml:lang="en">Koike N, Fukumura D, Gralla O et al. Tissue engineering: creation of longlasting blood vessels. Nature 2004; 428, 138–139</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Kojima K, Vacanti CA.Tissue engineering in the trachea. Anat Rec 2014; 297, 44–50</mixed-citation><mixed-citation xml:lang="en">Kojima K, Vacanti CA.Tissue engineering in the trachea. Anat Rec 2014; 297, 44–50</mixed-citation></citation-alternatives></ref><ref id="cit76"><label>76</label><citation-alternatives><mixed-citation xml:lang="ru">Tapias LF, Ott HC. Decellularized scaffolds as a platform for bioengineered organs. Curr Opin Organ Transplant 2014; 19, 145–152</mixed-citation><mixed-citation xml:lang="en">Tapias LF, Ott HC. Decellularized scaffolds as a platform for bioengineered organs. Curr Opin Organ Transplant 2014; 19, 145–152</mixed-citation></citation-alternatives></ref><ref id="cit77"><label>77</label><citation-alternatives><mixed-citation xml:lang="ru">Ross EA, Williams MJ, Hamazaki T et al. Embryonic stem cells proliferate and differentiate when seeded into kidney scaffolds. J Am Soc Nephrol 2014; 20, 2338–2347</mixed-citation><mixed-citation xml:lang="en">Ross EA, Williams MJ, Hamazaki T et al. Embryonic stem cells proliferate and differentiate when seeded into kidney scaffolds. J Am Soc Nephrol 2014; 20, 2338–2347</mixed-citation></citation-alternatives></ref><ref id="cit78"><label>78</label><citation-alternatives><mixed-citation xml:lang="ru">Song JJ, Guyette JP, Gilpin SE et al. Regeneration and experimental orthotopic transplantation of a bioengineered kidney. Nat Med 2013; 19, 646–651</mixed-citation><mixed-citation xml:lang="en">Song JJ, Guyette JP, Gilpin SE et al. Regeneration and experimental orthotopic transplantation of a bioengineered kidney. Nat Med 2013; 19, 646–651</mixed-citation></citation-alternatives></ref><ref id="cit79"><label>79</label><citation-alternatives><mixed-citation xml:lang="ru">Burgkart R, Tron A, Prodinger P et al. Decellularized kidney matrix for perfused bone engineering. Tissue Eng Part C Methods 2014; 20, 553–561</mixed-citation><mixed-citation xml:lang="en">Burgkart R, Tron A, Prodinger P et al. Decellularized kidney matrix for perfused bone engineering. Tissue Eng Part C Methods 2014; 20, 553–561</mixed-citation></citation-alternatives></ref><ref id="cit80"><label>80</label><citation-alternatives><mixed-citation xml:lang="ru">Bonandrini B, Figliuzzi M, Papadimou E et al. Recellularization of wellpreserved acellular kidney scaffold using embryonic stem cells. Tissue Eng Part A 2014; 20, 1486–1498</mixed-citation><mixed-citation xml:lang="en">Bonandrini B, Figliuzzi M, Papadimou E et al. Recellularization of wellpreserved acellular kidney scaffold using embryonic stem cells. Tissue Eng Part A 2014; 20, 1486–1498</mixed-citation></citation-alternatives></ref><ref id="cit81"><label>81</label><citation-alternatives><mixed-citation xml:lang="ru">Caralt M, Uzarski JS, Iacob S et al. Optimization and critical evaluation of decellularization strategies to develop renal extracellular matrix scaffolds as biological templates for organ engineering and transplantation. Am J Transplant 2014; 15, 64–75</mixed-citation><mixed-citation xml:lang="en">Caralt M, Uzarski JS, Iacob S et al. Optimization and critical evaluation of decellularization strategies to develop renal extracellular matrix scaffolds as biological templates for organ engineering and transplantation. Am J Transplant 2014; 15, 64–75</mixed-citation></citation-alternatives></ref><ref id="cit82"><label>82</label><citation-alternatives><mixed-citation xml:lang="ru">Peloso A, Ferrario J, Maiga B et al. Creation and implantation of acellular rat renal ECM-based scaffolds. Organogenesis 2015; 1, 58–74</mixed-citation><mixed-citation xml:lang="en">Peloso A, Ferrario J, Maiga B et al. Creation and implantation of acellular rat renal ECM-based scaffolds. Organogenesis 2015; 1, 58–74</mixed-citation></citation-alternatives></ref><ref id="cit83"><label>83</label><citation-alternatives><mixed-citation xml:lang="ru">Guan Y, Liu S, Sun C et al. The effective bioengineering method of implantation decellularized renal extracellular matrix scaffolds. Oncotarget 2015; 6, 36126–36138</mixed-citation><mixed-citation xml:lang="en">Guan Y, Liu S, Sun C et al. The effective bioengineering method of implantation decellularized renal extracellular matrix scaffolds. Oncotarget 2015; 6, 36126–36138</mixed-citation></citation-alternatives></ref><ref id="cit84"><label>84</label><citation-alternatives><mixed-citation xml:lang="ru">Sullivan DC, Mirmalek-Sani SH, Deegan DB et al. Decellularization methods of porcine kidneys for whole organ engineering using a high-throughput system. Biomaterials 2012; 33, 7756–7764</mixed-citation><mixed-citation xml:lang="en">Sullivan DC, Mirmalek-Sani SH, Deegan DB et al. Decellularization methods of porcine kidneys for whole organ engineering using a high-throughput system. Biomaterials 2012; 33, 7756–7764</mixed-citation></citation-alternatives></ref><ref id="cit85"><label>85</label><citation-alternatives><mixed-citation xml:lang="ru">Orlando G, Farney AC, Iskandar SS et al. Production and implantation of renal extracellular matrix scaffolds from porcine kidneys as a platform for renal bioengineering investigations. Ann Surg 2012; 256, 363–370</mixed-citation><mixed-citation xml:lang="en">Orlando G, Farney AC, Iskandar SS et al. Production and implantation of renal extracellular matrix scaffolds from porcine kidneys as a platform for renal bioengineering investigations. Ann Surg 2012; 256, 363–370</mixed-citation></citation-alternatives></ref><ref id="cit86"><label>86</label><citation-alternatives><mixed-citation xml:lang="ru">Guan Y, Liu S, Liu Y et al. Porcine kidneys as a source of ECM scaffold for kidney regeneration. Mater Sci Eng C Mater Biol Appl 2015; 56, 451–456</mixed-citation><mixed-citation xml:lang="en">Guan Y, Liu S, Liu Y et al. Porcine kidneys as a source of ECM scaffold for kidney regeneration. Mater Sci Eng C Mater Biol Appl 2015; 56, 451–456</mixed-citation></citation-alternatives></ref><ref id="cit87"><label>87</label><citation-alternatives><mixed-citation xml:lang="ru">Nakayama KH, Batchelder CA, Lee CI, Tarantal AF. Decellularized rhesus monkey kidney as a three-dimensional scaffold for renal tissue engineering. Tissue Eng Part A 2010; 16, 2207–2216</mixed-citation><mixed-citation xml:lang="en">Nakayama KH, Batchelder CA, Lee CI, Tarantal AF. Decellularized rhesus monkey kidney as a three-dimensional scaffold for renal tissue engineering. Tissue Eng Part A 2010; 16, 2207–2216</mixed-citation></citation-alternatives></ref><ref id="cit88"><label>88</label><citation-alternatives><mixed-citation xml:lang="ru">Orlando G, Booth C, Wang Z et al. Discarded human kidneys as a source of ECM scaffold for kidney regeneration technologies. Biomaterials 2013; 34, 5915–5925</mixed-citation><mixed-citation xml:lang="en">Orlando G, Booth C, Wang Z et al. Discarded human kidneys as a source of ECM scaffold for kidney regeneration technologies. Biomaterials 2013; 34, 5915–5925</mixed-citation></citation-alternatives></ref><ref id="cit89"><label>89</label><citation-alternatives><mixed-citation xml:lang="ru">Peloso A, Petrosyan A, Da Sacco S et al. Renal extracellular matrix scaffolds from discarded kidneys maintain glomerular morphometry and vascular resilience and retains critical growth factors. Transplantation 2015; 99, 1807–1816</mixed-citation><mixed-citation xml:lang="en">Peloso A, Petrosyan A, Da Sacco S et al. Renal extracellular matrix scaffolds from discarded kidneys maintain glomerular morphometry and vascular resilience and retains critical growth factors. Transplantation 2015; 99, 1807–1816</mixed-citation></citation-alternatives></ref><ref id="cit90"><label>90</label><citation-alternatives><mixed-citation xml:lang="ru">Crapo PM, Gilbert TW, Badylak SF. An overview of tissue and whole organ decellularization processes. Biomaterials 2012; 32, 3233–3243</mixed-citation><mixed-citation xml:lang="en">Crapo PM, Gilbert TW, Badylak SF. An overview of tissue and whole organ decellularization processes. Biomaterials 2012; 32, 3233–3243</mixed-citation></citation-alternatives></ref><ref id="cit91"><label>91</label><citation-alternatives><mixed-citation xml:lang="ru">He M, Callanan A. Comparison of methods for whole-organ decellularization in tissue engineering of bioartificial organs. Tissue Eng Part B Rev 2013; 19, 194–208</mixed-citation><mixed-citation xml:lang="en">He M, Callanan A. Comparison of methods for whole-organ decellularization in tissue engineering of bioartificial organs. Tissue Eng Part B Rev 2013; 19, 194–208</mixed-citation></citation-alternatives></ref><ref id="cit92"><label>92</label><citation-alternatives><mixed-citation xml:lang="ru">Keane TJ, Swinehart I, Badylak SF. Methods of tissue decellularization used for preparation of biologic scaffolds and in-vivo relevance. Methods 2015; 84, 25–34</mixed-citation><mixed-citation xml:lang="en">Keane TJ, Swinehart I, Badylak SF. Methods of tissue decellularization used for preparation of biologic scaffolds and in-vivo relevance. Methods 2015; 84, 25–34</mixed-citation></citation-alternatives></ref><ref id="cit93"><label>93</label><citation-alternatives><mixed-citation xml:lang="ru">Nakayama KH, Lee CCI, Batchelder CA, Tarantal AF. Tissue specificity of decellularized rhesus monkey kidney and lung scaffolds. PLoS One 2013; 8, e64134</mixed-citation><mixed-citation xml:lang="en">Nakayama KH, Lee CCI, Batchelder CA, Tarantal AF. Tissue specificity of decellularized rhesus monkey kidney and lung scaffolds. PLoS One 2013; 8, e64134</mixed-citation></citation-alternatives></ref><ref id="cit94"><label>94</label><citation-alternatives><mixed-citation xml:lang="ru">O’Neill JD, Freytes DO, Anandappa AJ et al. The regulation of growth and metabolism of kidney stem cells with regional specificity using extracellular matrix derived from kidney. Biomaterials 2013; 34, 9830–9841</mixed-citation><mixed-citation xml:lang="en">O’Neill JD, Freytes DO, Anandappa AJ et al. The regulation of growth and metabolism of kidney stem cells with regional specificity using extracellular matrix derived from kidney. Biomaterials 2013; 34, 9830–9841</mixed-citation></citation-alternatives></ref><ref id="cit95"><label>95</label><citation-alternatives><mixed-citation xml:lang="ru">Yu YL, Shao YK, Ding YQ et al. Decellularized kidney scaffold-mediated renal regeneration. Biomaterials 2014; 35, 6822–6828</mixed-citation><mixed-citation xml:lang="en">Yu YL, Shao YK, Ding YQ et al. Decellularized kidney scaffold-mediated renal regeneration. Biomaterials 2014; 35, 6822–6828</mixed-citation></citation-alternatives></ref><ref id="cit96"><label>96</label><citation-alternatives><mixed-citation xml:lang="ru">Abolbashari M, Agcaoili SM, Lee MK et al. Repopulation of porcine kidney scaffold using porcine primary renal cells. Acta Biomater 2016; 29, 52–61</mixed-citation><mixed-citation xml:lang="en">Abolbashari M, Agcaoili SM, Lee MK et al. Repopulation of porcine kidney scaffold using porcine primary renal cells. Acta Biomater 2016; 29, 52–61</mixed-citation></citation-alternatives></ref><ref id="cit97"><label>97</label><citation-alternatives><mixed-citation xml:lang="ru">Ross EA, Abrahamson DR, St. John P et al. Mouse stem cells seeded into decellularized rat kidney scaffolds endothelialize and remodel basement membranes. Organogenesis 2012; 8, 49–55</mixed-citation><mixed-citation xml:lang="en">Ross EA, Abrahamson DR, St. John P et al. Mouse stem cells seeded into decellularized rat kidney scaffolds endothelialize and remodel basement membranes. Organogenesis 2012; 8, 49–55</mixed-citation></citation-alternatives></ref><ref id="cit98"><label>98</label><citation-alternatives><mixed-citation xml:lang="ru">Bijonowski BM, Miller WM, Wertheim JA. Bioreactor design for perfusion-based, highly vascularized organ regeneration. Curr Opin Chem Eng 2013; 2, 32–40</mixed-citation><mixed-citation xml:lang="en">Bijonowski BM, Miller WM, Wertheim JA. Bioreactor design for perfusion-based, highly vascularized organ regeneration. Curr Opin Chem Eng 2013; 2, 32–40</mixed-citation></citation-alternatives></ref><ref id="cit99"><label>99</label><citation-alternatives><mixed-citation xml:lang="ru">Pollock CA. Toward a bioartificial kidney: will embryonic stem cells be the answer? Kidney 2013; Int 83, 543–545</mixed-citation><mixed-citation xml:lang="en">Pollock CA. Toward a bioartificial kidney: will embryonic stem cells be the answer? Kidney 2013; Int 83, 543–545</mixed-citation></citation-alternatives></ref><ref id="cit100"><label>100</label><citation-alternatives><mixed-citation xml:lang="ru">Badylak SF, Taylor D, Uygun K. Wholeorgan tissue engineering: decellularization and recellularization of three-dimensional matrix scaffolds. Annu Rev Biomed Eng 2011; 13, 27–53</mixed-citation><mixed-citation xml:lang="en">Badylak SF, Taylor D, Uygun K. Wholeorgan tissue engineering: decellularization and recellularization of three-dimensional matrix scaffolds. Annu Rev Biomed Eng 2011; 13, 27–53</mixed-citation></citation-alternatives></ref><ref id="cit101"><label>101</label><citation-alternatives><mixed-citation xml:lang="ru">Murphy SV, Atala A. 3D bioprinting of tissues and organs. Nat Biotechnol 2014; 32, 773–785</mixed-citation><mixed-citation xml:lang="en">Murphy SV, Atala A. 3D bioprinting of tissues and organs. Nat Biotechnol 2014; 32, 773–785</mixed-citation></citation-alternatives></ref><ref id="cit102"><label>102</label><citation-alternatives><mixed-citation xml:lang="ru">Groll J, Boland T, Blunk T et al. Biofabrication: reappraising the definition of an evolving field. Biofabrication 2016; 8, 013001</mixed-citation><mixed-citation xml:lang="en">Groll J, Boland T, Blunk T et al. Biofabrication: reappraising the definition of an evolving field. Biofabrication 2016; 8, 013001</mixed-citation></citation-alternatives></ref><ref id="cit103"><label>103</label><citation-alternatives><mixed-citation xml:lang="ru">Skardal A, Atala A. Biomaterials for integration with 3-D bioprinting. Ann Biomed Eng 2015; 43, 730–746</mixed-citation><mixed-citation xml:lang="en">Skardal A, Atala A. Biomaterials for integration with 3-D bioprinting. Ann Biomed Eng 2015; 43, 730–746</mixed-citation></citation-alternatives></ref><ref id="cit104"><label>104</label><citation-alternatives><mixed-citation xml:lang="ru">Chung JHY, Naficy S, Yue Z et al. Bio-ink properties and printability for extrusion printing living cells. Biomater Sci 2013; 1, 763</mixed-citation><mixed-citation xml:lang="en">Chung JHY, Naficy S, Yue Z et al. Bio-ink properties and printability for extrusion printing living cells. Biomater Sci 2013; 1, 763</mixed-citation></citation-alternatives></ref><ref id="cit105"><label>105</label><citation-alternatives><mixed-citation xml:lang="ru">Ferris CJ, Gilmore KJ, Beirne S et al. Bio-ink for ondemand printing of living cells. Biomater Sci 2013; 1, 224</mixed-citation><mixed-citation xml:lang="en">Ferris CJ, Gilmore KJ, Beirne S et al. Bio-ink for ondemand printing of living cells. Biomater Sci 2013; 1, 224</mixed-citation></citation-alternatives></ref><ref id="cit106"><label>106</label><citation-alternatives><mixed-citation xml:lang="ru">Pati F, Jang J, Ha D-H, et al. Printing threedimensional tissue analogues with decellularized extracellular matrix bioink. Nat Commun 2014; 5, 3935</mixed-citation><mixed-citation xml:lang="en">Pati F, Jang J, Ha D-H, et al. Printing threedimensional tissue analogues with decellularized extracellular matrix bioink. Nat Commun 2014; 5, 3935</mixed-citation></citation-alternatives></ref><ref id="cit107"><label>107</label><citation-alternatives><mixed-citation xml:lang="ru">Fullhase C, Soler R, Atala A et al. A novel hybrid printing system for the generation of organized bladder tissue. J Urol 2009; 181, 282–283</mixed-citation><mixed-citation xml:lang="en">Fullhase C, Soler R, Atala A et al. A novel hybrid printing system for the generation of organized bladder tissue. J Urol 2009; 181, 282–283</mixed-citation></citation-alternatives></ref><ref id="cit108"><label>108</label><citation-alternatives><mixed-citation xml:lang="ru">Williams SK, Touroo JS, Church KH, Hoying JB. Encapsulation of adipose stromal vascular fraction cells in alginate hydrogel spheroids using a direct-write three-dimensional printing system. Biores Open Access 2013; 2, 448–454</mixed-citation><mixed-citation xml:lang="en">Williams SK, Touroo JS, Church KH, Hoying JB. Encapsulation of adipose stromal vascular fraction cells in alginate hydrogel spheroids using a direct-write three-dimensional printing system. Biores Open Access 2013; 2, 448–454</mixed-citation></citation-alternatives></ref><ref id="cit109"><label>109</label><citation-alternatives><mixed-citation xml:lang="ru">Mironov V, Visconti RP, Kasyanov V et al. Organ printing: tissue spheroids as building blocks. Biomaterials 2009; 30, 2164–2174</mixed-citation><mixed-citation xml:lang="en">Mironov V, Visconti RP, Kasyanov V et al. Organ printing: tissue spheroids as building blocks. Biomaterials 2009; 30, 2164–2174</mixed-citation></citation-alternatives></ref><ref id="cit110"><label>110</label><citation-alternatives><mixed-citation xml:lang="ru">Faulkner-Jones A, Greenhough S, King JA et al. Development of a valve-based cell printer for the formation of human embryonic stem cell spheroid aggregates. Biofabrication 2013; 5, 015013</mixed-citation><mixed-citation xml:lang="en">Faulkner-Jones A, Greenhough S, King JA et al. Development of a valve-based cell printer for the formation of human embryonic stem cell spheroid aggregates. Biofabrication 2013; 5, 015013</mixed-citation></citation-alternatives></ref><ref id="cit111"><label>111</label><citation-alternatives><mixed-citation xml:lang="ru">Faulkner-Jones A, Fyfe C, Cornelissen DJ, Gardner et al. Bioprinting of human pluripotent stem cells and their directed differentiation into hepatocyte-like cells for the generation of minilivers in 3D. Biofabrication 2015; 7, 044102</mixed-citation><mixed-citation xml:lang="en">Faulkner-Jones A, Fyfe C, Cornelissen DJ, Gardner et al. Bioprinting of human pluripotent stem cells and their directed differentiation into hepatocyte-like cells for the generation of minilivers in 3D. Biofabrication 2015; 7, 044102</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
