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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Cell and Tissue Biology</journal-id><journal-title-group><journal-title xml:lang="en">Cell and Tissue Biology</journal-title><trans-title-group xml:lang="ru"><trans-title>Цитология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0041-3771</issn><issn publication-format="electronic">3034-6061</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">669569</article-id><article-id pub-id-type="doi">10.31857/S0041377123020037</article-id><article-id pub-id-type="edn">LWOREJ</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Development of Method for Three-Dimensional Cultivation of Human Mesenchymal Stem/Stromal Cells Using Cellulose Scaffolds</article-title><trans-title-group xml:lang="ru"><trans-title>Разработка метода трехмерного культивирования мезенхимных стволовых (стромальных) клеток человека с использованием матрицы из целлюлозы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kuneev</surname><given-names>I. K.</given-names></name><name xml:lang="ru"><surname>Кунеев</surname><given-names>И. К.</given-names></name></name-alternatives><email>aldomnina@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ivanova</surname><given-names>J. S.</given-names></name><name xml:lang="ru"><surname>Иванова</surname><given-names>Ю. С.</given-names></name></name-alternatives><email>aldomnina@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Nashchekina</surname><given-names>Y. A.</given-names></name><name xml:lang="ru"><surname>Нащекина</surname><given-names>Ю. А.</given-names></name></name-alternatives><email>aldomnina@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Patronova</surname><given-names>E. K.</given-names></name><name xml:lang="ru"><surname>Патронова</surname><given-names>Е. К.</given-names></name></name-alternatives><email>aldomnina@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Sokolova</surname><given-names>A. V.</given-names></name><name xml:lang="ru"><surname>Соколова</surname><given-names>А. В.</given-names></name></name-alternatives><email>aldomnina@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Domnina</surname><given-names>A. P.</given-names></name><name xml:lang="ru"><surname>Домнина</surname><given-names>А. П.</given-names></name></name-alternatives><email>aldomnina@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Institute of Cytology, Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">Институт цитологии РАН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-03-01" publication-format="electronic"><day>01</day><month>03</month><year>2023</year></pub-date><volume>65</volume><issue>2</issue><fpage>170</fpage><lpage>180</lpage><history><date date-type="received" iso-8601-date="2025-02-27"><day>27</day><month>02</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2023, И.К. Кунеев, Ю.С. Иванова, Ю.А. Нащекина, Е.К. Патронова, А.В. Соколова, А.П. Домнина</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, И.К. Кунеев, Ю.С. Иванова, Ю.А. Нащекина, Е.К. Патронова, А.В. Соколова, А.П. Домнина</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="en">И.К. Кунеев, Ю.С. Иванова, Ю.А. Нащекина, Е.К. Патронова, А.В. Соколова, А.П. Домнина</copyright-holder><copyright-holder xml:lang="ru">И.К. Кунеев, Ю.С. Иванова, Ю.А. Нащекина, Е.К. Патронова, А.В. Соколова, А.П. Домнина</copyright-holder></permissions><self-uri xlink:href="https://vietnamjournal.ru/0041-3771/article/view/669569">https://vietnamjournal.ru/0041-3771/article/view/669569</self-uri><abstract xml:lang="en"><p id="idm45181325808528">The development of methods for culturing cells in three-dimensional systems is an urgent focus of modern cell biology. When cultured in the 3D system, a tissue-specific architecture is reproduced and the real microenvironment and cell behavior <italic>in vivo</italic> are more precisely recreated. Human mesenchymal stem/stromal cells (MSCs) are typically isolated and cultured as a monolayer 2D culture. In this work, we developed a method for three-dimensional cultivation and tissue-specific decidual differentiation of MSCs isolated from human endometrial tissue using a matrix derived from decellularized apple. Decellularized apple matrices have sufficient mechanical strength, are biocompatible, accessible, easy to use, and have ample scope for surface modification. This cell culture system is suitable for both confocal microscopy and flow cytometry studies. The model we developed can become the basis for the creation of new cell products and tissue-engineering structures in the field of regenerative biomedicine.</p></abstract><trans-abstract xml:lang="ru"><p id="idm45181325806272">Разработка методов культивирования клеток в трехмерных системах важна и необходима для развития актуальных направлений современной клеточной биологии. При культивировании в системе 3D воспроизводится тканеспецифическая архитектура, точнее воссоздается реальная микросреда и поведение клеток <italic>in vivo</italic>. Мезенхимные стволовые/стромальные клетки человека (МСК) обычно выделяют и культивируют как монослойную 2D-культуру. В данной работе мы разработали метод трехмерного культивирования и тканеспецифической децидуальной дифференцировки МСК, выделенных из ткани эндометрия человека, с использованием матрицы, полученной из децеллюляризированного яблока. Матрицы из децеллюляризированного яблока обладают достаточной механической прочностью, биосовместимы, доступны, просты в использовании и имеют широкие возможности для модификации поверхности. Данная система культивирования клеток подходит как для их изучения методом конфокальной микроскопии, так и для исследований с помощью проточной цитометрии. Разработанная нами модель может стать основой для создания новых клеточных продуктов и тканеинженерных конструкций для нужд регенеративной биомедицины.</p></trans-abstract><kwd-group xml:lang="en"><kwd>3D cultivation</kwd><kwd>decellularized plants</kwd><kwd>endometrial mesenchymal stem/stromal cells</kwd><kwd>decidual differentiation</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>3D-культивирование</kwd><kwd>децеллюляризированные растения</kwd><kwd>эндометриальные мезенхимные стволовые (стромальные) клетки</kwd><kwd>децидуальная дифференцировка</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Коллекция культур клеток позвоночных ЦКП Института цитологии РАН (Санкт-Петербург), из которой получены эМСК, поддержана Минобрнауки РФ (Соглашение № 075-15-2021-683).</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Домнина А.П., Новикова П.В., Фридлянская И.И., Шилина М.А., Зенин В.В. 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