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<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">vavilov</journal-id><journal-title-group><journal-title xml:lang="ru">Вавиловский журнал генетики и селекции</journal-title><trans-title-group xml:lang="en"><trans-title>Vavilov Journal of Genetics and Breeding</trans-title></trans-title-group></journal-title-group><issn pub-type="epub">2500-3259</issn><publisher><publisher-name>Institute of Cytology and Genetics of Siberian Branch of the RAS</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.18699/VJ18.344</article-id><article-id custom-type="elpub" pub-id-type="custom">vavilov-1438</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>КЛЕТОЧНАЯ И МОЛЕКУЛЯРНАЯ БИОЛОГИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CELL AND MOLECULAR BIOLOGY</subject></subj-group></article-categories><title-group><article-title>Церебральные органоиды – перспективная модель в клеточных технологиях</article-title><trans-title-group xml:lang="en"><trans-title>Cerebral organoids: a promising model in cellular technologies</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>Шнайдер</surname><given-names>Т. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Shnaider</surname><given-names>T. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Новосибирск</p></bio><bio xml:lang="en"><p>Novosibirsk</p></bio><email xlink:type="simple">shnayder.t@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru">Федеральный исследовательский центр Институт цитологии и генетики Сибирского отделения Российской академии наук<country>Россия</country></aff><aff xml:lang="en">Institute of Cytology and Genetics SB RAS<country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>06</day><month>04</month><year>2018</year></pub-date><volume>22</volume><issue>2</issue><fpage>168</fpage><lpage>178</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Шнайдер Т.А., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Шнайдер Т.А.</copyright-holder><copyright-holder xml:lang="en">Shnaider T.A.</copyright-holder><license 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://vavilov.elpub.ru/jour/article/view/1438">https://vavilov.elpub.ru/jour/article/view/1438</self-uri><abstract><p>Развитие головного мозга человека представляет собой сложный многоэтапный процесс, включающий образование различных типов нейральных клеток и их взаимодействия. Многие фундаментальные механизмы нейрогенеза установлены благодаря изучению модельных животных. Однако значительные структурные различия головного мозга по сравнению с другими животными не позволяют рассмотреть все аспекты формирования головного мозга у человека, которые могут играть решающую роль для развития его уникальных когнитивных способностей. Новая технология трехмерных церебральных органоидов открывает исследователям уникальную возможность моделировать ранние этапы нейрогенеза человека. В обзоре рассматриваются технология получения трехмерных церебральных органоидов, примеры ее успешного внедрения в фундаментальные и прикладные исследования, имеющиеся проблемы, а также перспективы ее развития.</p></abstract><trans-abstract xml:lang="en"><p>The development of the human brain is a complex multi-stage process including the formation of various types of neural cells and their interactions. Many fundamental mechanisms of neurogenesis have been established due to the studying of model animals. However, significant differences in the brain structure compared to other animals do not allow considering all aspects of the human brain formation, which could play the main role in the development of unique cognitive abilities for human. Four years ago, Lancaster’s group elaborated human pluripotent stem cell-derived three-dimensional cerebral organoid technology, which opened a unique opportunity for researchers to model early stages of human neurogenesis in vitro. Cerebral organoids closely remodel many endogenous brain regions with specific cell composition like ventricular zone with radial glia, choroid plexus, and cortical plate with upper and deeper-layer neurons. Moreover, human brain development includes interactions between different brain regions. Generation of hybrid three-dimensional cerebral organoids with different brain region identity allows remodeling some of them, including long-distance neuronal migration or formation of major axonal tracts. In this review, we consider the technology of obtaining human pluripotent stem cell-derived three-dimensional cerebral organoids with different modifications and with different brain region identity. In addition, we discuss successful implementation of this technology in fundamental and applied research like modeling of different neurodevelopmental disorders and drug screening. Finally, we regard existing problems and prospects for development of human pluripotent stem cell-derived threedimensional cerebral organoid technology.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>нейрогенез</kwd><kwd>церебральные органоиды</kwd><kwd>клеточные технологии</kwd></kwd-group><kwd-group xml:lang="en"><kwd>neurogenesis</kwd><kwd>cerebral organoids</kwd><kwd>cellular technologies</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Abud E.M., Ramirez R.N., Martinez E.S., Healy L.M., Nguyen C.H.H., Newman S.A., Yeromin A.V., Scarfone V.M., Marsh S.E., Fimbres C., Caraway C.A., Fote G.M., Madany A.M., Agrawal A., Kayed R., Gylys K.H., Cahalan M.D., Cummings B.J., Antel J.P., Mortazavi A., Carson M.J., Poon W.W., Blurton-Jones M. iPSC-derived human microglia-like cells to study neurological diseases. Neuron. 2017;94(2):278-293.e9. 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