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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">669533</article-id><article-id pub-id-type="doi">10.31857/S0041377123060068</article-id><article-id pub-id-type="edn">QNYLGA</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">Review of Local Cellular and Molecular Processes of Bone Tissue Regeneration Induced by Calcium Phosphate Materials</article-title><trans-title-group xml:lang="ru"><trans-title>Обзор локальных клеточно-молекулярных процессов регенерации костной ткани, индуцированных кальцийфосфатными материалами</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Miroshnichenko</surname><given-names>L. A.</given-names></name><name xml:lang="ru"><surname>Мирошниченко</surname><given-names>Л. А.</given-names></name></name-alternatives><email>larisalitvinova@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Polyakova</surname><given-names>T. Yu.</given-names></name><name xml:lang="ru"><surname>Полякова</surname><given-names>Т. Ю.</given-names></name></name-alternatives><email>larisalitvinova@yandex.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Litvinova</surname><given-names>L. S.</given-names></name><name xml:lang="ru"><surname>Литвинова</surname><given-names>Л. С.</given-names></name></name-alternatives><email>larisalitvinova@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Khlusov</surname><given-names>I. A.</given-names></name><name xml:lang="ru"><surname>Хлусов</surname><given-names>И. А.</given-names></name></name-alternatives><email>larisalitvinova@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Laboratory of Cellular and Microfluidic Technologies, Siberian State Medical University</institution></aff><aff><institution xml:lang="ru">Лаборатория клеточных и микрофлюидных технологий, Сибирский государственный медицинский университет</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Department of Normal Physiology, Siberian State Medical University</institution></aff><aff><institution xml:lang="ru">Кафедра нормальной физиологии, Сибирский государственный медицинский университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-11-01" publication-format="electronic"><day>01</day><month>11</month><year>2023</year></pub-date><volume>65</volume><issue>6</issue><fpage>557</fpage><lpage>572</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, Л.А. Мирошниченко, Т.Ю. Полякова, Л.С. Литвинова, И.А. Хлусов</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, Л.А. Мирошниченко, Т.Ю. Полякова, Л.С. Литвинова, И.А. Хлусов</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="en">Л.А. Мирошниченко, Т.Ю. Полякова, Л.С. Литвинова, И.А. Хлусов</copyright-holder><copyright-holder xml:lang="ru">Л.А. Мирошниченко, Т.Ю. Полякова, Л.С. Литвинова, И.А. Хлусов</copyright-holder></permissions><self-uri xlink:href="https://vietnamjournal.ru/0041-3771/article/view/669533">https://vietnamjournal.ru/0041-3771/article/view/669533</self-uri><abstract xml:lang="en"><p id="idm45257549464432">One of the leading causes of hospitalization, disability and mortality of 50% of women and 20% of men over the age of 50 are bone fractures and their complications caused by diseases of the musculoskeletal system. In this regard, an active search for a solution to the problem associated with the limitations of the use of auto-, allo-, and xenografts in the clinic to replace bone defects initiated the development of a regenerative approach based on the gradual replacement of artificial material with growing bone tissue. Promising in this regard are materials based on calcium phosphates, which act as an active source of chemical elements (calcium, phosphorus, etc.), which can optimize the process of bone defect fusion and ensure the replacement of the implant with new bone tissue. The review summarizes literature data on local biological activity, target cells, and molecular effects of calcium phosphates. It has been shown that calcium phosphate materials are biocompatible, capable of adsorbing regulatory proteins and cells, influencing their genetic and secretory apparatus and triggering the process of MSC differentiation in the osteogenic direction. At the same time, the successful implementation of local mechanisms of osseointegration at the “bone/implant” interface reduces the risk of periprosthetic infection (PJI) and rejection of artificial devices. Further study and use of calcium phosphate materials will make it possible to make a significant breakthrough in solving modern problems of bone tissue regeneration associated with an accurate (digital) bioengineering approach based on additive technologies and artificial intelligence.</p></abstract><trans-abstract xml:lang="ru"><p id="idm45257549464496">Одной из ведущих причин госпитализации, инвалидизации и смертности 50% женщин и 20% мужчин в возрастной группе старше 50 лет являются переломы костей и их осложнения, обусловленные заболеваниями опорно-двигательной системы. Активный поиск решения проблемы, связанной с ограничениями применения в клинике ауто-, алло- и ксенотрансплантатов, для замещения костных дефектов, инициировал развитие регенеративного подхода, основанного на постепенном замещении искусственного материала растущей костной тканью. Перспективными в этом отношении являются материалы на основе фосфатов кальция, выполняющие роль активного источника химических элементов (кальций, фосфор и др.), способные оптимизировать процесс срастания костного дефекта и обеспечить замену имплантата новой костной тканью. В представленном обзоре обобщены данные из литературы о локальной биологической активности, клетках-мишенях и молекулярных эффектах фосфатов кальция. Показано, что кальцийфосфатные материалы биосовместимы, способны адсорбировать регуляторные белки и клетки, оказывая влияние на их генетический и секреторный аппарат и запуская процесс дифференцировки МСК в остеогенном направлении. При этом успешная реализация локальных механизмов остеоинтеграции на границе раздела кость–имплантат снижает риск перипротезной инфекции и отторжения искусственных изделий. Дальнейшее изучение и использование кальцийфосфатных материалов позволит осуществить значительный прорыв в решении современных проблем регенерации костной ткани, связанный с точным (цифровым) биоинженерным подходом на основе аддитивных технологий и искусственного интеллекта.</p></trans-abstract><kwd-group xml:lang="en"><kwd>calcium phosphate materials</kwd><kwd>osteoinduction</kwd><kwd>osteogenic cells</kwd><kwd>osteogenesis</kwd><kwd>regeneration</kwd><kwd>mesenchymal stem cells</kwd><kwd>cellular and molecular mechanisms</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>кальцийфосфатные материалы</kwd><kwd>остеиндукция</kwd><kwd>остеогенные клетки</kwd><kwd>остеогенез</kwd><kwd>регенерация</kwd><kwd>мезенхимные стволовые клетки</kwd><kwd>клеточно-молекулярные механизмы</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Добринская М.Н. 2018. Влияние новых нанодисперсных допированных макро- и микроэлементами карбонат-фосфатов кальция на организм экспериментальных животных. Автореф. канд. дис. Екатеренбург. 20 с. (Dobrinskaya M.N. Influence of new nanosized calcium carbonate-phosphates doped with macro- and microelements on the body of experimental animals. Ph. D. Thesis. Yekaterinburg. 20 pp.).</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Дьячкова У.Д., Виговский М.А., Басалова Н. А., Григорьева О.А., Ефименко А.Ю. 2022. Внеклеточные везикулы МСК переключают фенотип макрофагов с провоспалительного на противовоспалительный. Гены и клетки. Т. 7. № 3. С. 81. (Dyachkova U.D., Vigovsky M.A., Basalova N.A., Grigorieva O.A., Efimenko A.Yu. 2022. MSC extracellular vesicles switch the macrophage phenotype from pro-inflammatory to anti-inflammatory. Genes and cells. V. 7. No 3. P. 81.)</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Иванюк Е.Э., Надеждин С.В., Покровская Л.А., Шуплецова В.В., Хазиахматова О.Г., Юрова К.А., Малащенко В.В., Литвинова Л.С., Хлусов И.А. 2018. Субпопуляции макрофагов и мезенхимные стволовые клетки в регуляции ремоделирования костной ткани. Цитология. Т. 60. № 4. С. 252. (Ivanyuk E.E., Nadezhdin S.V., Pokrovskaya L.A., Shupletsova V.V., Khaziakhmatova O.G., Yurova K.A., Malashchenko V.V., Litvinova L.S., Khlusov I.A. 2018. Macrophage subpopulations and mesenchymal stem cells in the regulation of bone tissue remodeling. Tsitologiya. V. 60. № 4. P. 252).</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Карлов А.В., Хлусов И.А. 2003. Зависимость процессов репаративного остеогенеза от поверхностных свойств имплантатов для остеосинтеза. Гений ортопедии № 3. С. 46. (Karlov A.V., Khlusov I.A. 2003. Dependence of the processes of reparative osteogenesis on the surface properties of implants for osteosynthesis. Orthopedic genius. № 3. P. 46).</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Корель А.В., Кузнецов С.Б. 2019. Тканеинженерные стратегии для восстановления дефектов костной ткани. Cовременное состояние вопроса. Межд. журн. прикладных и фунд. иссл. № 4. С. 228. (Korel A.V., Kuznetsov S.B. 2019. Tissue engineering strategies for the restoration of bone defects. The current state of the issue. International J. Applied Basic Res. № 4. Р. 228).</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Пичугин В.Ф., Сурменева М.A., Сурменев Р.А., Хлусов И.А., Эппле М. 2011. Исследование физико-химических и биологических свойств кальцийфосфатных покрытий, созданных методом ВЧ-магнетронного распыления кремнийзамещенного гидроксиапатита. Поверхность. Рентгеновские, синхротронные и нейтронные исследования. № 9. С. 54 (Pichugin V.F., Surmeneva M.A., Surmenev R.A., Khlusov I.A., Epple M. 2011. Study of physicochemical and biological properties of calcium phosphate coatings prepared by RF magnetron sputtering of silicon-substituted hydroxyapatite. J. Surf. Investig. № 5. Р. 863.).</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Юрова К.А., Хазиахматова О.Г., Малащенко В.В., Норкин И.К., Иванов П.А., Хлусов И.А., Шунькин Е.О., Тодосенко Н.М., Мелащенко Е.С., Литвинова Л.С. 2020. Клеточно-молекулярные аспекты воспаления, ангиогенеза и остеогенеза. Краткий обзор. Цитология. Т. 62. № 5. С. 305. (Yurova K.A., Khaziakhmatova O.G., Malashchenko V.V., Norkin I.K., Ivanov P.A., Khlusov I.A., Shunkin E.O., Todosenko N.M., Melashchenko E.S., Litvinova L.S. 2020. Cellular and molecular aspects of inflammation, angiogenesis and osteogenesis. Short review. Tsitologiya. V. 62. № 5. Р. 305.).</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Albee F.H. 1920. Studies in bone growth: triple calcium phosphate as a stimulus to osteogenesis. Ann. Surg. V. 71. P. 32.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Anderson J.M., Rodriguez A., Chang D.T. 2008. Foreign body reaction to biomaterials. Seminars Immunol. V. 20. P. 86.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Barradas A.M., Fernandes H.A., Groen N., Chai Y.C., Schrooten J., van de Peppel J., van Leeuwen J.V., van Blitterswijk C.V., de Boer J. 2012. A calcium-induced signaling cascade leading to osteogenic differentiation of human bone marrow-derived mesenchymal stromal cells. Biomaterials. V. 33. P. 3205.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Barradas A.M., Yuan H., van Blitterswijk C.A.C., Habibovic P. 2011. Osteoinductive biomaterials: current knowledge of properties, experimental models and biological mechanisms. Eur. Cells Mater. V. 21. P. 407.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Batoon L., Millard S.M., Raggatt L.J., Pettit A.R. 2017a. Osteomacs and bone regeneration. Curr. Osteoporos Rep. V. 15. P. 385.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Batoon L., Millard S.M., Wullschleger M.E., Preda C., Wu A.C.-K, Kaur S., Tseng H.-W., Hume D.A., Levesque J.-P., Raggatt L.J., Pettit A.R. 2017b. CD169 + macrophages are critical for osteoblast maintenance and promote intramembranous and endochondral ossification during bone repair. Biomaterials. V. 196. P. 51.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Bellows C.G., Aubin J.E., Heersche J.N. 1991.Initiation and progression of mineralization of bone nodules formed in vitro: the role of alkaline phosphatase and organic phosphate. Bone Min. V. 14. P. 27.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Ben-Nissan B. 2014. Advances in calcium phosphate biomaterials. Springer Berlin: Heidelberg. P. 547.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Berube P., Yang Y., Carnes D.L., Stover R.E., Boland E.J., Ong J.L. 2005. The effect of sputtered calcium phosphate coatings of different crystallinity on osteoblast differentiation. J. Periodontol. V. 76. P. 1697.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Bianchi M., Urquia Edreira E.R., Wolke J.G., Birgani Z.T., Habibovic P., Jansen J.A., Tampieri A., Marcacci M., Leeuwenburgh S.C., van den Beucken J.J. 2014. Substrate geometry directs the in vitro mineralization of calcium phosphate ceramics. Acta Biomater. V. 10. P. 661.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Bohner M., Miron R.J. 2018. A proposed mechanism for material-induced heterotopic ossification, Mater. Today. V. 22. P. 132.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Boix T., Gomez-Morales J., Torrent-Burgues J., Monfort A., Pulgdomenech P., Rodriguez-Clemente R. 2005. Adsorption of recombinant human bone morphogenetic protein rhBMP-2m onto hydroxyapatite. J. Inorg. Biochem. V. 9. P. 1043.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Bulnheim U., Müller P., Neumann H.-G., Peters K., Unger R.E., Kirkpatrick C.J., Rychly J. 2012. Endothelial cells stimulate osteogenic differentiation of mesenchymal stem cells on calcium phosphate scaffolds. J. Tissue Engineering and Regener. Med. V. 8. P. 831.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Campana V., Milano G., Pagano E., Barba M., Cicione C., Salonna G., Lattanzi W., Logroscino G. 2014. Bone substitutes in orthopaedic surgery: from basic science to clinical practice. J. Mater. Sci. Mater Med. V. 25. P. 2445.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Chai Y.C., Roberts S.J., Schrooten J., Luyten F.P. 2011. Probing the osteoinductive effect of calcium phosphate by using an in vitro biomimetic model. Tiss. Eng. A. V. 17. P. 1083.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Chang D.T., Jones J.A., Meyerson H., Colton E., Kwon I.K., Matsuda T., Anderson J.M. 2008. Lymphocyte/macrophage interactions: biomaterial surface-dependent cytokine, chemokine, and matrix protein production. J. Biomed. Mater. Res. A. V. 87. P. 676.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Chen L., Mccrate J.M., Lee J.C., Li H. 2011. The role of surface charge on the uptake and biocompatibility of hydroxyapatite nanoparticles with osteoblast cells. Nanotechnol. V. 22: 105708.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Chen Z., Wu C., Gu W., Klein T., Crawford R., Xiao Y. 2014. Osteogenic differentiation of bone marrow MSCs by beta-tricalcium phosphate stimulating macrophages via BMP2 signalling pathway. Biomaterials. V. 35. P. 1507.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Combes C., Ray C. 2002. Adsorption of proteins and calcium phosphate materials bioactivity. Biomaterials. V. 23. P. 2817.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Coughlan T., Dockery F. 2014. Osteoporosis and fracture risk in older people. Clin. Med. (Lond). V. 14. P. 187.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Curtis A., Wilkinson C. 1997. Topographical control of cells. Biomaterials. V. 18. P. 1573.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Daculsi G., Legeros R.Z., Nery E., Lynch K., Kerebel B. 1989. Transformation of biphasic calcium phosphate ceramics in vivo: ultrastructural and physicochemical characterization. J. Biomed. Mater. Res. V. 23. P. 883.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Danciu T.E., Adam R.M., Naruse K., Freeman M.R., Hauschka P.V. 2003. Calcium regulates the PI3K-Akt pathway in stretched osteoblasts. FEBS Lett. V. 536. P. 193.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Davies L.C., Rosas M., Jenkins S.J., Liao C.T., Scurr M.J., Brombacher F., Fraser D.J., Allen J.E., Jones S.A., Taylor Ph.R. 2013. Distinct bone marrow-derived and tissue-resident macrophage lineages proliferate at key stages during inflammation. Nat. Commun. V. 4. P. 1886.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Davison N.L., Gamblin A.L., Layrolle P., Yuan H., de Bruijn J.D., Barrere-de Groot F. 2014. Liposomal clodronate inhibition of osteoclastogenesis and osteoinduction by submicrostructured beta-tricalcium phosphate. Biomaterials. V. 35. P. 5088.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Diaz-Flores L., Gutierrez R., Lopez-Alonso A., Gonzalez R., Varela H. 1992. Pericytes as a supplementary source of osteoblasts in periosteal osteogenesis. Clin. Orthop. Relat. Res. V. 275. P. 280.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Dimitriou R., Tsiridis E., Giannoudis P.V. 2005. Current concepts of molecular aspects of bone healing. Injury. V. 36. P. 1392.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Du C., Cui F.Z., Zhang W., Feng Q.L., Zhu X.D., de Groot K. 2000. Formation of calcium phosphate/collagen composites through mineralization of collagen matrix. J. Biomed. Mater. Res. V. 50. P. 518.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Ebrahimi M. 2021. Porosity parameters in biomaterial science: Definition, impact, and challenges in tissue engineering. Front. Mater. Sci. V. 15. P. 352.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Edwards F.C., Taheri A., Dann S.C., Dye J.F. 2011. Characterization of cytolytic neutrophil activation in vitro by amorphous hydrated calcium phosphate as a model of biomaterial inflammation. J. Biomed. Mater. Res. A. V. 96. P. 552.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Ekegren C.L., Edwards E.R., de Steiger R., Gabbe B.J. 2018. Incidence, costs and predictors of non-union, delayed union and mal-union following long bone fracture. Int. J. Environ. Res. Public Health. V. 15. P. 2845.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>El-Rashidy A.A., Roether J.A., Harhaus L., Kneser U., Boccaccini A.R. 2017. Regenerating bone with bioactive glass scaffolds: a review of in vivo studies in bone defect models. Acta Biomater. V. 62. P. 1.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Fellah B.H., Gauthier O., Weiss P., Chappard D., Layrolle P. 2008. Osteogenicity of biphasic calcium phosphate ceramics and bone autograft in a goat model. Biomaterials. V. 29. P. 1177.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Feng B., Weng J., Yang B.C., Qu S.X., Zhang X.D. 2004. Characterization of titanium surfaces with calcium and phosphate and osteoblast adhesion. Biomaterials. V. 25. P. 3421.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Feng W. 2014. Osteoclastogenesis and osteoimmunology. Front. Biosci. V. 19. P. 758.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Fillingham Y., Jacobs J. 2014. Bone grafts and their substitutes. J. Indian Soc. Periodontol. V. 18. P. 610.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Flade K., Lau C., Mertig M., Pompe W. 2001. Osteocalcin-controlled dissolution-reprecipitation of calcium phosphate under biometric conditions. Chem. Mater. V. 13. P. 3596.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Foreman M.A., Gu A.Y., Howl J.D., Jones S., Publicover S.J. 2005. Group III metabotropic glutamate receptor activation inhibits Ca2+ influx and nitric oxide synthase activity in bone marrow stromal cells. J. Cell Physiol. V. 204. P. 704.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Gamblin A.-L., Brennan M.A., Renaud A., Yagita H., Lézot F., Heymann D., Trichet V., Layrolle P. 2014. Bone tissue formation with human mesenchymal stem cells and biphasic calcium phosphate ceramics: the local implication of osteoclasts and macrophages. Biomaterials. V. 35. P. 9660.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Garg P., Mazur M.M., Buck A.C., Wandtke M.E., Liu J., Ebraheim N.A. 2017. Prospective review of mesenchymal stem cells differentiation into osteoblasts. Orthop Surg. V. 9. P. 13.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Ghosh S.K., Nandi S.K., Kundu B., Datta S., De D.K., Roy S.K., Basu D. 2008. In vivo response of porous hydroxyapatite and beta-tricalcium phosphate prepared by aqueous solution combustion method and comparison with bioglass scaffolds. J. Biomed. Mater. Res. B. Appl. Biomater. V. 86. P. 217.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Goding J.W., Grobben B., Slegers H. 2003. Physiological and pathophysiological functions of the ecto-nucleotide pyrophosphatase/phosphodiesterase family. Biochim. Biophys. Acta Mol. Basis Dis. V. 1638. P. 1.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Gustavsson J., Ginebra M. P., Planell J., Engel E. 2012. Osteoblast-like cellular response to dynamic changes in the ionic extracellular environment produced by calcium-deficient hydroxyapatite. JMSMM. V. 23. P. 2509.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Habibovic P., Sees T.M., van den Doel M.A., van Blitterswijk C.A., de Groot J.K. 2006. Osteoinduction by biomaterials–physicochemical and structural influences. Biomed. Mater. Res. A. V. 77. P. 747.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Hasegawa T., Hongo H., Yamamoto T., Abe M., Yoshino H., Haraguchi-Kitakamae M., Ishizu H., Shimizu T., Iwasaki N., Amizuka N. 2022. Matrix vesicle-mediated mineralization and osteocytic regulation of bone mineralization. Int. J. Mol. Sci. V. 23. P. 9941.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Henriksen K., Karsdal M.A., John Martin T. 2014. Osteoclast-derived coupling factors in bone remodeling. Calcif. Tiss. Int. V. 94 P. 88.</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Hu Q.H., Tan Z., Liu Y.K., Tao J.H., Cai Y.R., Zhang M., Pan H., Xu X., Tang R. 2007. Effect of crystallinity of calcium phosphate nanoparticles on adhesion, proliferation, and differentiation of bone marrow mesenchymal stem cells. J. Mater. Chem. V. 17. P. 4690.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Humbert P., Brennan M.Á., Davison N., Rosset Ph., Trichet V., Blanchard F., Layrolle P. 2019. immune modulation by transplanted calcium phosphate biomaterials and human mesenchymal stromal cells in bone regeneration. Front. Immunol. V. 10. P. 663.</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Ikebuchi Y., Aoki S., Honma M., Hayashi M., Sugamori Y., Khan M., Kariya Y., Kato G., Tabata Y., Penninger J.M., Udagawa N., Aoki K., Suzuki H. 2018. Coupling of bone resorption and formation by RANKL reverse signalling. Nature. V. 561. P. 195.</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>James A.W. 2013. Review of signaling pathways governing MSC osteogenic and Adipogenic differentiation. Scientifica (Cairo). 2013: 684736.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Jensen S.S., Bosshardt D.D., Gruber R., Buser D. 2014. Long-term stability of contour augmentation in the esthetic zone: histologic and histomorphometric evaluation of 12 human biopsies 14 to 80 months after augmentation. J. Periodontol. V. 85. P. 1549.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Jeong J., Kim J.H., Shim J.H., Hwang N.S., Heo C.Y. 2019. Bioactive calcium phosphate materials and applications in bone regeneration. Biomater. Res. V. 23. P. 4.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>John A., Varma H.K., Kumari T.V. 2003. Surface reactivity of calcium phosphate based ceramics in a cell culture system. J. Biomater. V. 18. P. 63.</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Julien M., Khoshniat S., Lacreusette A., Gatius M., Bozec A., Wagner E.F., Wittrant Y., Masson M., Weiss P., Beck L., Magne D., Guicheux J. 2009. Phosphate-dependent regulation of MGP in osteoblasts: role of ERK1/2 and Fra-1. J. Bone Miner. Res. V. 24. P. 1856.</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Jung G.Y., Park Y.J., Han J.S. 2010. Effects of HA released calcium ion on osteoblast differentiation. J. Mater. Sci. Mater. Med. V. 21. P. 1649.</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Kandori K., Miyagawa K., Ishikawa T. 2004. Adsorption of immunogamma globulin onto various synthetic calcium hydroxyapatite particles. J. Colloid. Interface Sci. V. 273. P. 406.</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Kandori K., Murata K., Ishikawa T. 2007. Microcalorimetric study of protein adsorption onto calcium hydroxyapatites. Langmuir. V. 23. P. 2064.</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Karalashvili L., Kakabadze A., Uhryn M., Vyshnevska H., Ediberidze K., Kakabadze Z. 2018. Bone grafts for reconstruction of bone defects (review). Georgian Med. News. V. 282. P. 44.</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Katsuyama E., Miyamoto H., Kobayashi T., Sato Y., Hao W., Kanagawa H., Fujie A., Tando T., Watanabe R., Morita M., Miyamoto K., Niki Y., Morioka H., Matsumoto M., Toyama Y. et al. 2015. Interleukin-1 receptor-associated kinase-4 (IRAK4) promotes inflammatory osteolysis by activating osteoclasts and inhibiting formation of foreign body giant cells. J. Biol. Chem. V. 290. P. 716.</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Khlusov I.A., Khlusova M.Yu., Zaitsev K.V., Kolokol’tsova T.D., Sharkeev Yu.P., Pichugin V.F., Legostaeva E.V., Trofi mova I.E., Klimov A.S., Zhdanova A.I. 2011. Pilot in vitro study of the parameters of artificial niche for osteogenic differentiation of human stromal stem cell pool. Bull. Exp. Biol. Med. V. 150. P. 535.</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Khlusov I.A., Litvinova L.S., Shupletsova V.V., Khaziakhmatova O.G., Malashchenko V.V., Yurova K.A., Shunkin E.O., Krivosheev V.V., Porokhova E.D., Sizikova A.E., Safiullina L.A., Legostaeva E.V., Komarova E.G., Sharkeev Yu.P. 2020. Costimulatory effect of rough calcium phosphate coating and blood mononuclear cells on adipose-derived mesenchymal stem cells in vitro as a model of in vivo tissue repair. Materials. V. 13. P. 4398.</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Khlusov I.A., Litvinova L.S., Yurova K.A., Khlusova M.Y. 2022. Precise tissue bioengineering and niches of mesenchymal stem cells: their size and hierarchy matter. Biocell. V. 46. P. 1635.</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Khlusov I.A., Shevtsova N.M., Khlusova M.Y. 2013. Detection in vitro and quantitative estimation of artificial microterritories which promote osteogenic differentiation and maturation of stromal stem cells. Methods Mol. Biol. V. 1035. P. 103.</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Khlusov I.A., Dekhtyar Y., Sharkeev Y.P., Pichugin V.F., Khlusova M.Y., Polyaka N., Tjulkins F., Vendinya V., Legostaeva E.V., Litvinova L.S., Shupletsova V.V., Khaziakhmatova O.G., Yurova K.A., Prosolov K.A. 2018. Nanoscale electrical potential and roughness of a calcium phosphate surface promotes the osteogenic phenotype of stromal cells. Materials. V. 11. P. 978.</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Khoshniat S., Bourgine A., Julien M., Petit M., Pilet P., Rouillon T., Masson M., Gatius M., Weiss P., Guicheux J., Beck L. 2011. Phosphatedependent stimulation of MGP and OPN expression in osteoblasts via the ERK1/2 pathway is modulated by calcium. Bone. V. 48. P. 894.</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Kim S.E., Park K. 2020. Recent advances of biphasic calcium phosphate bioceramics for bone tissue regeneration. Adv. Exp. Med. Biol. V. 1250. P. 177.</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Knabe C., Driessens F.C.M., Planell J. A., Gildenhaar R., Berger G., Reif D., Fitzner R., Radlanski R.J., Gross U. 2000. Evaluation of calcium phosphates and experimental calcium phosphate bone cements using osteogenic cultures. J. Biomed. Mater. Res. V. 52. P. 498.</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Komarova E.G., Sharkeev Y.P., Sedelnikova M.B., Prymak O., Epple M., Litvinova L.S., Shupletsova V.V, Malashchenko V.V., Yurova K.A., Dzyuman A.N., Kulagina I.V., Mushtovatova L.S., Bochkareva O.P., Karpova M.R., Khlusov I.A. 2020. Zn- or Cu-containing CaP-based coatings formed by micro-arc oxidation on titanium and Ti-40Nb alloy: part II – wettability and biological performance. Materials. V. 13. P. 4366.</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Kuroda Y., Hisatsune Ch., Nakamura T., Matsuo K., Mikoshiba K. 2008. Osteoblasts induce Ca2+ oscillation-independent NFATc1 activation during osteoclastogenesis. Proc. Natl. Acad Sci. USA. V. 105. P. 8643.</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Li B., Liao X.L., Zheng L., Zhu X. D., Wang Z., Fan H.S., Zhang X. 2012. Effect of nanostructure on osteoinduction of porous biphasic calcium phosphate ceramics. Acta Biomater. V. 8. P. 3794.</mixed-citation></ref><ref id="B78"><label>78.</label><mixed-citation>Litvinova L., Yurova K., Shupletsova V., Khaziakhmatova O., Malashchenko V., Shunkin E., Melashchenko E., Todosenko N., Khlusova M., Sharkeev Y., Komarova E., Sedelnikova M., Khlusov I. 2020. Gene expression regulation and secretory activity of mesenchymal stem cells upon in vitro contact with microarc calcium phosphate coating. Int. J. Mol. Sci. V. 21. P. 7682.</mixed-citation></ref><ref id="B79"><label>79.</label><mixed-citation>Liu D., Genetos D.C., Shao Y., Geist D.J., Li J., Ke H.Zh., Turner Ch.H., Duncan R.L. 2008. Activation of extracellular-signal regulated kinase (ERK1/2) by fluid shear is Ca2+ and ATP-dependent in MC3T3-E1 osteoblasts. Bone. V. 42. P. 644.</mixed-citation></ref><ref id="B80"><label>80.</label><mixed-citation>Liu Q., Lu W.F., Zhai W. 2022. Toward stronger robocast calcium phosphate scaffolds for bone tissue engineering: A mini-review and meta-analysis. Biomater. Adv. V. 134. P. 112 578.</mixed-citation></ref><ref id="B81"><label>81.</label><mixed-citation>Liu Y.K., Lu Q.Z., Pei R., Ji H.J., Zhou G.S., Zhao X.L., Tang R.K., Zhang M. 2009. The effect of extracellular calcium and inorganic phosphate on the growth and osteogenic differentiation of mesenchymal stem cells in vitro: implication for bone tissue engineering. Biomed. Mater. V. 4: 025004.</mixed-citation></ref><ref id="B82"><label>82.</label><mixed-citation>MacLauchlan S., Skokos E.A., Meznarich N., Zhu D.H., Raoof S., Shipley J.M., Senior R.M., Bornstein P., Kyriakides Th.R. 2009. Macrophage fusion, giant cell formation, and the foreign body response require matrix metalloproteinase 9. J. Leukoc. Biol. V. 85. P. 617.</mixed-citation></ref><ref id="B83"><label>83.</label><mixed-citation>Mafina M.K., Sullivan A.C., Hing K.A. 2017. Use of a fluorescent probe to monitor the enhanced affinity of rh-BMP-2 to silicated-calcium phosphate synthetic bone graft substitutes under competitive conditions. Mater. Sci. Eng. C Mater. Biol. Appl. V. 80. P. 207.</mixed-citation></ref><ref id="B84"><label>84.</label><mixed-citation>Maggiano I.S., Maggiano C.M., Clement J.G., Thomas C.D., Carter Y., Cooper D.M. 2016. Three-dimensional reconstruction of Haversian systems in human cortical bone using synchrotron radiation-based micro-CT: morphology and quantification of branching and transverse connections across age. J. Anat. May. V. 228. P. 719.</mixed-citation></ref><ref id="B85"><label>85.</label><mixed-citation>Majidinia M., Sadeghpour A., Yousefi B. 2018. The roles of signaling pathways in bone repair and regeneration. J. Cell Physiol. V. 233. P. 2937.</mixed-citation></ref><ref id="B86"><label>86.</label><mixed-citation>Maloney M.A., Dorie M.J., Lamela R.A., Rogers Z.R., Patt H.M. 1978. Hematopoietic stem cell regulatory volumes as revealed in studies of the bgj/bgj:W/WV chimera. J. Exp. Med. V. 147. P. 1189.</mixed-citation></ref><ref id="B87"><label>87.</label><mixed-citation>Mao L., Liu J., Zhao J., Chang J., Xia L., Jiang L., Wang X., Lin K., Fang B. 2015. Effect of micro-nano-hybrid structured hydroxyapatite bioceramics on osteogenic and cementogenic differentiation of human periodontal ligament stem cell via Wnt signaling pathway. Int. J. Nanomedicine. V. 8. P. 1887.</mixed-citation></ref><ref id="B88"><label>88.</label><mixed-citation>Marino G., Rosso F., Cafiero G., Tortora C., Moraci M., Barbarisi M., Barbarisi A. 2010. Beta-tricalcium phosphate 3D scaffold promote alone osteogenic differentiation of human adipose stem cells: in vitro study. J. Mater. Sci. Mater. Med. V. 21. P. 353.</mixed-citation></ref><ref id="B89"><label>89.</label><mixed-citation>Matsuura T., Hosokawa R., Okamoto K., Kimoto T., Akagawa Y. 2000. Diverse mechanisms of osteoblast spreading on hydroxyapatite and titanium. Biomaterials. V. 21. P. 1121.</mixed-citation></ref><ref id="B90"><label>90.</label><mixed-citation>McNally A.K., Anderson J.M. 1995. Interleukin-4 induces foreign body giant cells from human monocytes/macrophages. Differential lymphokine regulation of macrophage fusion leads to morphological variants of multinucleated giant cells. Am. J. Pathol. V. 147. P. 1487.</mixed-citation></ref><ref id="B91"><label>91.</label><mixed-citation>McNally A.K., Anderson J.M. 2011. Foreign body-type multinucleated giant cells induced by interleukin-4 express select lymphocyte co-stimulatory molecules and are phenotypically distinct from osteoclasts and dendritic cells. Exp. Mol. Pathol. V. 91. P. 673.</mixed-citation></ref><ref id="B92"><label>92.</label><mixed-citation>McNally A.K., Jones J.A., MacEwan S.R., Colton E., Anderson J.M. 2008. Vitronectin is a critical protein adhesion substrate for IL-4-induced foreign body giant cell formation. J. Biomed. Mater. Res. A. V. 86A. P. 35.</mixed-citation></ref><ref id="B93"><label>93.</label><mixed-citation>McNally A.K., Macewan S.R., Anderson J.M. 2007. Alpha subunit partners to beta1 and beta2 integrins during IL-4-induced foreign body giant cell formation. J. Biomed. Mater. Res. Part A. V. 82. P. 568.</mixed-citation></ref><ref id="B94"><label>94.</label><mixed-citation>Meleti Z., Shapiro M., Adams C.S. 2000. Inorganic phosphate induces apoptosis of osteoblast-like cells in culture. Bone. V. 27. P. 359.</mixed-citation></ref><ref id="B95"><label>95.</label><mixed-citation>Millan C., Vivanco J.F., Benjumeda-Wijnhoven I.M., Bjelica S., Santibanez J.F. 2018. Mesenchymal stem cells and calcium phosphate bioceramics: implications in periodontal bone regeneration. Adv. Exp. Med. Biol. V. 1107. P. 91.</mixed-citation></ref><ref id="B96"><label>96.</label><mixed-citation>Miron R.J., Bosshardt D.D. 2016. OsteoMacs: key players around bone biomaterials. Biomaterials. V. 82. P. 1.</mixed-citation></ref><ref id="B97"><label>97.</label><mixed-citation>Moreno J.L., Mikhailenko I., Tondravi M.M., Keegan A.D. 2007. IL-4 promotes the formation of multinucleated giant cells from macrophage precursors by a STAT6-dependent, homotypic mechanism: contribution of E-cadherin. J. Leukoc. Biol. V. 82. P. 1542.</mixed-citation></ref><ref id="B98"><label>98.</label><mixed-citation>Murshed M. 2018. Mechanism of bone mineralization. Cold Spring Harb. Perspect. Med. V. 8: a031229. Erratum in: Cold Spring Harb. Perspect. Med. 2020. V. 10.</mixed-citation></ref><ref id="B99"><label>99.</label><mixed-citation>Najar M., Raicevic G., Crompot E., Fayyad-Kazan H., Bron D., Toungouz M., Lagneaux L. 2016. The immunomodulatory potential of mesenchymal stromal cells. J. Immunother. V. 39. P. 45.</mixed-citation></ref><ref id="B100"><label>100.</label><mixed-citation>Nich C., Takakubo Y., Pajarinen J., Ainola M., Salem A., Sillat T., Rao A.J., Raska M., Tamaki Y., Takagi M., Konttinen Y.T., Goodman St.B., Gallo J. 2013. Macrophages-key cells in the response to wear debris from joint replacements. J. Biomed. Mater. Res. A. V. 101. P. 3033.</mixed-citation></ref><ref id="B101"><label>101.</label><mixed-citation>Nudelman F., Pieterse K., George A., Bomans P.H.H., Friedrich H., Brylka L.J., Hilbers P.A.J., de With G., Sommerdijk N.A.J.M. 2010. The role of collagen in bone apatite formation in the presence of hydroxyapatite nucleation inhibitors. Nat. Mater. V. 9. P. 1004.</mixed-citation></ref><ref id="B102"><label>102.</label><mixed-citation>Ogata K., Katagiri W., Hibi H. 2017. Secretomes from mesenchymal stem cells participate in the regulation of osteoclastogenesis in vitro. Clin. Oral Investig. V. 21. P. 1979.</mixed-citation></ref><ref id="B103"><label>103.</label><mixed-citation>Okamoto K., Takayanagi H. 2019. Osteoimmunology. Cold Spring Harb. Perspect. Med. V. 9: a031245.</mixed-citation></ref><ref id="B104"><label>104.</label><mixed-citation>Orimo H. 2010. The mechanism of mineralization and the role of alkaline phosphatase in health and disease. J. Nippon Med. Sch. V. 77. P. 4.</mixed-citation></ref><ref id="B105"><label>105.</label><mixed-citation>Othman Z., Fernandes H., Groot Arjan J, Luider Theo M., Alcinesio A., de Melo Pereira D., Guttenplan Al.P.M., Yuan H., Habibovic P. 2019. The role of ENPP1/PC-1 in osteoinduction by calcium phosphate ceramics Biomaterials. V. 210. P. 12.</mixed-citation></ref><ref id="B106"><label>106.</label><mixed-citation>Pajarinen J., Lin T., Gibon E., Kohno Y., Maruyama M., Nathan K., Lu L., Yao Zh., Goodman St.B. 2018. Mesenchymal stem cell-macrophage crosstalk and bone healing. Biomaterials. V. 196. P. 80.</mixed-citation></ref><ref id="B107"><label>107.</label><mixed-citation>Pchelintseva E., Djamgoz M.B.A. 2018. Mesenchymal stem cell differentiation: Control by calcium-activated potassium channels. J. Cell Physiol. V. 233. P. 3755.</mixed-citation></ref><ref id="B108"><label>108.</label><mixed-citation>Polini A., Pisignano D., Parodi M., Quarto R., Scaglione S. 2011. Osteoinduction of human mesenchymal stem cells by bioactive composite scaffolds without supplemental osteogenic growth factors. PLoS One. V. 6: e26211.</mixed-citation></ref><ref id="B109"><label>109.</label><mixed-citation>Quinn JM.W., Itoh K., Udagawa N., Häusler K., Yasuda H., Shima N., Mizuno A., Higashio K., Takahashi N., Suda T., Martin T.J., Gillespie M.T. 2001. Transforming growth factor β affects osteoclast differentiation via direct and indirect actions. J. Bone Miner. Res. V. 16. P. 1787.</mixed-citation></ref><ref id="B110"><label>110.</label><mixed-citation>Rana N., Suliman S., Mohamed-Ahmed S., Gavasso S., Gjertsen B.T., Mustafa K. 2022. Systemic and local innate immune responses to surgical co-transplantation of mesenchymal stromal cells and biphasic calcium phosphate for bone regeneration. Acta Biomater. Actions. V. 141. P. 440.</mixed-citation></ref><ref id="B111"><label>111.</label><mixed-citation>Raphel J., Holodniy M., Goodman S.B., Heilshorn S.C. 2016. Multifunctional coatings to simultaneously promote osseointegration and prevent infection of orthopaedic implants. Biomaterials. V. 84. P. 301.</mixed-citation></ref><ref id="B112"><label>112.</label><mixed-citation>Ratner B.D., Hoffman A.S., Schoen F., Lemons J. (Eds.) 2004. Biomaterials science: an introduction to materials in medicine. San Diego, CA, USA: Elsevier Acad. Press. 864 p.</mixed-citation></ref><ref id="B113"><label>113.</label><mixed-citation>Ripamonti U., Roden L.C. 2010. Induction of bone formation by transforming growth factor-beta2 in the non-human primate Papio ursinus and its modulation by skeletal muscle responding stem cells. Cell Prolif. V. 43. P. 207.</mixed-citation></ref><ref id="B114"><label>114.</label><mixed-citation>Ripamonti U., Roden L.C., Ferretti C., Klar R.M. 2011. Biomimetic matrices self-initiating the induction of bone formation. J. Craniofac. Surg. V. 22. P. 1859.</mixed-citation></ref><ref id="B115"><label>115.</label><mixed-citation>Rodriguez A., Macewan S.R., Meyerson H., Kirk J.T., Anderson J.M. 2009. The foreign body reaction in T-cell-deficient mice. J. Biomed. Mater. Res. A. V. 90. P. 106.</mixed-citation></ref><ref id="B116"><label>116.</label><mixed-citation>Sadowska J.M, Wei F., Guo J., Guillem-Marti J., Lin Zh., Ginebra M.-P., Xiao Y. 2019. The effect of biomimetic calcium deficient hydroxyapatite and sintered β-tricalcium phosphate on osteoimmune reaction and osteogenesis. Acta Biomater. V. 96. P. 605.</mixed-citation></ref><ref id="B117"><label>117.</label><mixed-citation>Salasznyk R.M., Klees R.F., Williams W.A., Boskey A., Plopper G.E. 2007. Focal adhesion kinase signaling pathways regulate the osteogenic differentiation of human mesenchymal stem cells. Exp. Cell Res. V. 313. P. 22.</mixed-citation></ref><ref id="B118"><label>118.</label><mixed-citation>Samavedi S., Whittington A.R., Goldstein A.S. 2013. Calcium phosphate ceramics in bone tissue engineering: a review of properties and their influence on cell behavior. Acta Biomater. V. 9. P. 8037.</mixed-citation></ref><ref id="B119"><label>119.</label><mixed-citation>Sapir-Koren R., Livshits G. 2011. Bone mineralization and regulation of phosphate homeostasis. IBMS BoneKEy. V. 8. P. 286.</mixed-citation></ref><ref id="B120"><label>120.</label><mixed-citation>Schemitsch E.H. 2017. Size matters: defining critical in bone defect size! J. Orthop. Trauma. V. 31. P. S20.</mixed-citation></ref><ref id="B121"><label>121.</label><mixed-citation>Shen B., Bhargav D., Wei A., Williams L. A., Tao H., Ma D.D.F., Diwan A.D. 2009. BMP-13 emerges as a potential inhibitor of bone formation. Int. J. Biol. Sci. V. 5. P. 192.</mixed-citation></ref><ref id="B122"><label>122.</label><mixed-citation>Shi F., Fang X., Zhou T., Huang X., Duan K., Wang J., Qu S., Zhi W., Weng J. 2022. Macropore regulation of hydroxyapatite osteoinduction via microfluidic pathway. Int. J. Mol. Sci. V. 23. P. 11459.</mixed-citation></ref><ref id="B123"><label>123.</label><mixed-citation>Silva L.H.A., Antunes M.A., Dos Santos C.C., Weiss D.J., Cruz F.F., Rocco P.R.M. 2018. Strategies to improve the therapeutic effects of mesenchymal stromal cells in respiratory diseases. Stem Cell Res. Ther. V. 9. P. 45.</mixed-citation></ref><ref id="B124"><label>124.</label><mixed-citation>Sims N.A., Martin T.J. 2014. Coupling the activities of bone formation and resorption: a multitude of signals within the basic multicellular unit. Bonekey Rep. V. 3. P. 1.</mixed-citation></ref><ref id="B125"><label>125.</label><mixed-citation>Sokolova V., Knuschke T., Kovtun A., Buer J., Epple M., Westendorf A.M. 2010. The use of calcium phosphate nanoparticles encapsulating Toll-like receptor ligands and the antigen hemagglutinin to induce dendritic cell maturation and T cell activation. Biomaterials. V. 31. P. 5627.</mixed-citation></ref><ref id="B126"><label>126.</label><mixed-citation>Stephansson S.N., Byers B.A., Garcia A.J. 2002. Enhanced expression of the osteoblastic phenotype on substrates that modulate fibronectin conformation and integrin receptor binding. Biomaterials. V. 23. P. 2527.</mixed-citation></ref><ref id="B127"><label>127.</label><mixed-citation>Tada H., Nemoto E., Foster B.L., Somerman M.J., Shimauchi H. 2011. Phosphate increases bone morphogenetic protein-2 expression through cAMP-dependent protein kinase and ERK1/2 pathways in human dental pulp cells. Bone. V. 48. P. 1409.</mixed-citation></ref><ref id="B128"><label>128.</label><mixed-citation>Takeshita S., Fumoto T., Matsuoka K., Park K., Aburatani H., Kato S., Ito M., Ikeda K. 2013. Osteoclast-secreted CTHRC1 in the coupling of bone resorption to formation. J. Clin. Invest. V. 123. P. 3914.</mixed-citation></ref><ref id="B129"><label>129.</label><mixed-citation>Teitelbaum S.L. 2005. Osteoporosis and integrins, J. Clin. Endocrinol. Metab. V. 90. P. 2466.</mixed-citation></ref><ref id="B130"><label>130.</label><mixed-citation>Ten Harkel B., Schoenmaker T., Picavet D.I., Davison N.L., de Vries T.J., Everts V. 2015. The foreign body giant cell cannot resorb bone, but dissolves hydroxyapatite like osteoclasts. PLoS ONE. V. 10: e0139564.</mixed-citation></ref><ref id="B131"><label>131.</label><mixed-citation>Thrivikraman G., Athirasala A., Twohig C., Boda S.K., Bertassoni L.E. 2017. Biomaterials for craniofacial bone regeneration. Dent Clin. North Am. V. 61. P. 835.</mixed-citation></ref><ref id="B132"><label>132.</label><mixed-citation>Tsapikouni T.S., Missirlis Y.F. 2008. Protein–material interactions: from micro-to-nano scale. Mater. Sci. Eng. B. V. 152. P. 2.</mixed-citation></ref><ref id="B133"><label>133.</label><mixed-citation>van Furth R., Cohn Z.A. 1968. The origin and kinetics of mononuclear phagocytes. J. Exper. Med. V. 128. P. 415.</mixed-citation></ref><ref id="B134"><label>134.</label><mixed-citation>Vasconcelos D.P., Costa M., Amaral I.F., Barbosa M.A., Aguas A.P., Barbosa J.N. 2015. Modulation of the inflammatory response to chitosan through M2 macrophage polarization using pro-resolution mediators. Biomaterials. V. 37. P. 116.</mixed-citation></ref><ref id="B135"><label>135.</label><mixed-citation>Viti F., Landini M., Mezzelani A., Petecchia L., Milanesi L., Scaglione S. 2016. Osteogenic differentiation of MSC through calcium signaling activation: transcriptomics and functional analysis. PLoS One. V. 11: e0148173.</mixed-citation></ref><ref id="B136"><label>136.</label><mixed-citation>Vulf M., Khlusov I., Yurova K., Todosenko N., Komar A., Kozlov I., Malashchenko V., Shunkina D., Khaziakhmatova O., Litvinova L. 2022. MicroRNA regulation of bone marrow mesenchymal stem cells in the development of osteoporosis in obesity. Front. Biosci. (Schol Ed). V. 14. P. 17.</mixed-citation></ref><ref id="B137"><label>137.</label><mixed-citation>Wang Y., Hu J., Jiao J., Liu Z., Zhou Z., Zhao C., Chang L.J., Chen Y.E., Ma P.X., Yang B. 2014. Engineering vascular tissue with functional smooth muscle cells derived from human iPS cells and nanofibrous scaffolds. Biomaterials. V. 35. P. 8960.</mixed-citation></ref><ref id="B138"><label>138.</label><mixed-citation>Xiao D., Zhang J., Zhang C., Barbieri D., Yuan H., Moroni L., Feng G. 2020. The role of calcium phosphate surface structure in osteogenesis and the mechanisms involved. Acta Biomater. V. 106. P. 22.</mixed-citation></ref><ref id="B139"><label>139.</label><mixed-citation>Yuan H.P., Fernandes H., Habibovic P., de Boer J., Barradas AM.C., de Ruiter A., Walsh W.R., van Blitterswijk C.A., de Bruijn J.D. 2010. Osteoinductive ceramics as a synthetic alternative to autologous bone grafting. Proc. Natl. Acad. Sci. USA. V. 107. P. 13614.</mixed-citation></ref><ref id="B140"><label>140.</label><mixed-citation>Yurova K.A., Melashchenko E.S., Khaziakhmatova O.G., Malashchenko V.V., Melashchenko O.B., Shunkin E.O., Norkin I.K., Ivanov P.A., Khlusov I.A., Litvinova L.S. 2021. Osteogenic differentiation factors of multipotent mesenchymal stromal cells in the current understanding. Curr. Pharm. Des. V. 27. P. 3741.</mixed-citation></ref><ref id="B141"><label>141.</label><mixed-citation>Zayzafoon M., Fulzele K., McDonald J.M. 2005. Calmodulin and calmodulin-dependent kinase IIalpha regulate osteoblast differentiation by controlling c-fos expression. J. Biol. Chem. V. 280. P. 7049.</mixed-citation></ref><ref id="B142"><label>142.</label><mixed-citation>Zhang R., Lu Y., Ye L., Yuan B., Yu Sh., Qin Ch., Xie Y., Gao T., Drezner M.K., Bonewald L.F., Feng J.Q. 2011. Unique roles of phosphorus in endochondral bone formation and osteocyte maturation. J. Bone Miner. Res. V. 26. P. 1047.</mixed-citation></ref><ref id="B143"><label>143.</label><mixed-citation>Zhang Y., Böse T., Unger R.E., Jansen J.A., Kirkpatrick C.J., van den Beucken J.P. 2017. Macrophage type modulates osteogenic differentiation of adipose tissue MSCs. Cell Tiss. Res. V. 369. P. 273.</mixed-citation></ref><ref id="B144"><label>144.</label><mixed-citation>Zhao L., Kaye A.D., Kaye A.J., Abd-Elsayed A. 2018. Stem cell therapy for osteonecrosis of the femoral head: current trends and comprehensive review. Curr. Pain Headache Rep. V. 22. P. 41.</mixed-citation></ref><ref id="B145"><label>145.</label><mixed-citation>Zhao Z., Zhao Q., Gu B., Yin C., Shen K., Tang H., Xia H., Zhang X., Zhao Y., Yang X., Zhang Y. 2020. Minimally invasive implantation and decreased inflammation reduce osteoinduction of biomaterial. Theranostics. V. 10. P. 3533.</mixed-citation></ref><ref id="B146"><label>146.</label><mixed-citation>Zhu X.D., Fan H.S., Li D.X., Xiao Y.M., Zhang X.D. 2007. Protein adsorption and zeta potentials of a biphasic calcium phosphate ceramic under various conditions. J. Biomed. Mater. Res B. V. 82B. P. 65.</mixed-citation></ref><ref id="B147"><label>147.</label><mixed-citation>Zhu X.D., Fan H.S., Xiao Y.M., Li D.X., Zhang H.J., Luxbacher T., Zhang X.D. 2009. Effect of surface structure on protein adsorption to biphasic calcium-phosphate ceramics in vitro and in vivo. Acta Biomater. V. 5. P. 1311.</mixed-citation></ref><ref id="B148"><label>148.</label><mixed-citation>Zhu X., Zhang H.J., Fan H.S., Li W., Zhang X.D. 2010. Effect of phase composition and microstructure of calcium phosphate ceramic particles on protein adsorption. Acta Biomater. V. 6. P. 1536.</mixed-citation></ref></ref-list></back></article>
