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    Academic Journal

    المساهمون: This work was supported by the Russian Science Foundation grant 17-15-01368P and the Russian Foundation for Basic Research 19-29-04164 (epicardial cell-based spheroids assembly)., Работа выполнена при финансовой поддержке гранта РНФ 17-15-01368П и РФФИ 19-29-04164 (сборка сфероидов на основе клеток эпикарда).

    المصدر: General Reanimatology; Том 17, № 6 (2021); 49-55 ; Общая реаниматология; Том 17, № 6 (2021); 49-55 ; 2411-7110 ; 1813-9779

    وصف الملف: application/pdf

    Relation: https://www.reanimatology.com/rmt/article/view/2159/1574; https://www.reanimatology.com/rmt/article/view/2159/1583; Derrick C.J., Noël E.S. The ECM as a driver of heart development and repair. Development. 2021; 148 (5): DOI:10.1242/dev.191320. PMID: 33674261.; Nair N. Epidemiology and pathogenesis of heart failure with preserved ejection fraction. Review. Cardiovasc Med. 2020; 21 (4): 531–540. DOI:10.31083/j.rcm.2020.04.154.; Mocumbi A.O., Stothard J.R., Correia-de-Sá P., Yacoub M. Endomyocardial Fibrosis: an Update After 70 Years.Curr Cardiol Rep. 2019; 21 (11): 148. DOI:10.1007/s11886-019-1244-3. PMID: 317583524.; Zhou B., A. von Gise., Ma Q., Hu Y.W., Pu W.T. Genetic fate mapping demonstrates contribution of epicardium-derived cells to the annulus fibrosis of the mammalian heart. Dev. Biol. 338 (2010) 251–261. DOI:10.1016/j.ydbio.2009.12.007. PMID: 20025864. PMCID: PMC2815244; Wessels. A, van den Hoff M.J., Adamo R.F., Phelps A.L., Lockhart M.M., Sauls K., Briggs L.E., Norris R.A., van Wijk B., Perez-Pomares J.M., Dettman R.W., Burch J.B. Epicardially derived fibroblasts preferentially contribute to the parietal leaflets of the atrioventricular valves in the murine heart. Dev. Biol. 2012; 366: 111–124. DOI:10.1016/j.ydbio.2012.04.020. PMID: 22546693. PMCID: PMC3358438; von Gise A., Zhou B., Honor L.B., Ma Q., Petryk A., Pu W.T. WT1 regulates epicardial epithelial to mesenchymal transition through betacatenin and retinoic acid signaling pathways, Dev. Biol. 2011; 356: 421–431. DOI:10.1016/j.ydbio.2011.05.668. PMID: 21663736. PMCID: PMC3147112; Braitsch C.M., Combs M.D., Quaggin, S.E., Yutzey K.E. Pod1/Tcf21 is regulated by retinoic acid signaling and inhibits differentiation of epicardium-derived cells into smooth muscle in the developing heart. Dev. Biol. 2012; 368: 345–357. DOI:10.1016/j.ydbio.2012.06.002. PMID: 22687751. PMCID: PMC3414197; Acharya, A., Baek, S.T., Huang, G., Eskiocak, B., Goetsch, S., Sung, C.Y., Banfi, S., Sauer M.F., OlsenG.S., Duffield J.S. The bHLH transcription factor Tcf21 is required for lineage-specific EMT of cardiac fibroblast progenitors. Development. 2012; 139: 2139–2149. DOI:10.1242/dev.079970. PMID: 22573622. PMCID: PMC3357908; Moore-Morris T., Cattaneo P., Guimaraes-Camboa N., Bogomolovas J., Cedenilla M., Banerjee I., Ricote M., Kisseleva T., Zhang L., Gu Y., Dalton N.D., Peterson K.L., Chen J., Puceat M., Evans S.M. Infarct fibroblasts do not derive from bone marrow lineages. Circ. Res. 2012; 122 (4): 583–590. DOI:10.1161/CIRCRESAHA.117.311490. PMID: 29269349. PMCID: PMC5815911; Moore-Morris T., Guimaraes-Camboa N., Banerjee I., Zambon A.C., Kisseleva T., Velayoudon A., Stallcup W.B., Gu Y. Dalton N.D, Cedenilla M., Gomez-Amaro R., Zhou B. Brenner D.A, Peterson K.L., Chen J., Evans S.M. Resident fibroblast lineages mediate pressure overloadinduced cardiac fibrosis. J Clin Invest. 2014; 124 (7): 2921–2934. DOI:10.1172/JCI7478.3. PMID: 24937432. PMCID: PMC4071409; Braitsch C.M., Kanisicak O., van Berlo J.H., Molkentin J.D, Yutzey K.E. Differential expression of embryonic epicardial progenitor markers and localization of cardiac fibrosis in adult ischemic injury and hypertensive heart disease. J. Mol. Cell. Cardiol. 2013; 65: 108–119. DOI:10.1016/j.yjmcc.2013.10.005. PMID: 24140724. PMCID: PMC3848425; Santi A.Li., Napolitano F., Montuori N., Ragno P. The Urokinase Receptor: A Multifunctional Receptor in Cancer Cell Biology. Therapeutic Implications. Int J Mol Sci. 2021; 22 (8): 4111. DOI:10.3390/ijms22084111. PMID: 33923400. PMCID: PMC8073738; Dergilev K.V., Stepanova V.V., Beloglazova I.B., Tsokolayev Z.I., Parfenova E.V. Multifaced Roles of the Urokinase System in the Regulation of Stem Cell Niches. Acta Naturae. 2018; 10 (4): 19–32. PMID: 30713759. PMCID: PMC6351041; Junqueira L.C., Bignolas G., Brentani R.R. Picrosirius staining plus polarization microscopy, a specific method for collagen detection in tissue sections. Histochem J. 1979; 11: 447–455. DOI:10.1007/bf01002772; Dergilev K.V., Tsokolaeva Z.I., Beloglazova I.B., Ratner E.I., Parfenova E.V. Transforming Growth Factor Beta (TGF-β1) Induces Pro-Reparative Phenotypic Changes in Epicardial Cells in Mice.Bull Exp Biol Med. 2021; 170 (4): 565–570. DOI:10.1007/s10517-021-05107-5.; Baart V.M., Houvast R.D., de Geus-Oei L.F., Quax P.H.A., Kuppen P.J.K., Vahrmeijer A.L., Sier C.F.M. Molecular imaging of the urokinase plasminogen activator receptor: opportunities beyond cancer. EJNMMI Res. 2020; 10 (1): 87. DOI:10.1186/s13550-020-00673-7. PMID: 32725278. PMCID: PMC7387399; Genua M., D'Alessio S., Cibella J., Gandelli A., Sala E., Correale C., Spinelli A., Arena V., Malesci A., Rutella S., Ploplis V.A., Vetrano S., Danese S. The urokinase plasminogen activator receptor (uPAR) controls macrophage phagocytosis in intestinal inflammation. Gut. 2015; 64 (4): 589–600. DOI:10.1136/gutjnl-2013-305933. PMID: 24848264; Jo M., Takimoto S., Montel V., Gonias S.L.The urokinase receptor promotes cancer metastasis independently of urokinase-type plasminogen activator in mice. Am J Pathol. 2009; 175 (1): 190–200. DOI:10.2353/ajpath.2009.081053. PMID: 19497996. PMCID: PMC2708805; Jo M., Lester R.D., Montel V., Eastman B., Takimoto S., Gonias S.L. Reversibility of epithelial-mesenchymal transition (EMT) induced in breast cancer cells by activation of urokinase receptor-dependent cell signaling J Biol Chem. 2009; 284 (34): 22825–22833 DOI:10.1074/jbc.M109.023960. PMID: 19546228. PMCID: PMC2755690; Hinz B., Phan S.H., Thannickal V.J., Prunotto M., Desmoulière A., Varga J., De Wever O., Mareel M., Gabbiani G. Recent developments in myofibroblast biology: paradigms for connective tissue remodeling. Am J Pathol. 2012; 180 (4): 1340–1355. DOI:10.1016/j.ajpath.2012.02.004. PMID: 22387320. PMCID: PMC3640252; Castella L.F., Buscemi L., Godbout C., Meister J.J., Hinz B. A new lockstep mechanism of matrix remodelling based on subcellular contractile events. J Cell Sci. 2010; 123 (Pt 10): 1751–1760. DOI:10.1242/jcs.066795. PMID: 20427321; Wang L., Ly C.M., Ko C.Y., Meyers E.E., Lawrence D.A., Bernstein A.M. uPA binding to PAI-1 induces corneal myofibroblast differentiation on vitronectin. Invest Ophthalmol Vis Sci. 2012; 53 (8): 4765–4775. DOI:10.1167/iovs.12-10042. PMID: 22700714. PMCID: PMC3949353; Stepanova V., Lebedeva T., Kuo A., Yarovoi S., Tkachuk S., Zaitsev S., Bdeir K., Dumler I., Marks M.S., Parfyonova Y., Tkachuk V.A., Higazi A.A., Cines D.B. Nuclear translocation of urokinase-type plasminogen activator. Blood. 2008; 112 (1): 100–110. DOI:10.1182/blood-2007-07-104455. PMID: 18337556. PMCID: PMC2435680; Semina E.V., Rubina K.A., Shmakova A.A., Rysenkova K.D., Klimovich P.S., Aleksanrushkina N. A., Sysoeva V. Y., Karagyaur M.N., Tkachuk V.A. Downregulation of uPAR promotes urokinase translocation into the nucleus and epithelial to mesenchymal transition in neuroblastoma. J Cell Physiol. 2020; 235 (9): 6268–6286. DOI:10.1002/jcp.29555. PMID: 31990070. PMCID: PMC7318179; Zhang G., Kernan K.A., Thomas A., Collins S., Song Y., Li L., Zhu W., Leboeuf R.C., Eddy A.A. A novel signaling pathway: fibroblast nicotinic receptor alpha1 binds urokinase and promotes renal fibrosis. J Biol Chem. 2009; 284 (42): 29050–29064. DOI:10.1074/jbc.M109.010249. PMID: 19690163. PMCID: PMC2781451; Manetti M., Rosa I., Fazi M., Guiducci S., Carmeliet P., Ibba-Manneschi L., Matucci-Cerinic M. Systemic sclerosis-like histopathological features in the myocardium of uPAR-deficient mice. Ann Rheum Dis. 2016; 75 (2): 474–478. DOI:10.1136/annrheumdis-2015-207803. PMID: 26269399; Mohameden M., Vashisht P., Sharman T. Scleroderma And Primary Myocardial Disease. 2021. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan. PMID: 32491618; Nikitorowicz-Buniak J., Denton C.P., Abraham D., Stratton R. Partially Evoked Epithelial-Mesenchymal Transition (EMT) Is Associated with Increased TGFβ Signaling within Lesional Scleroderma Skin. PLoS One. 2015; 10 (7): e0134092. DOI:10.1371/journal.pone.0134092. PMID: 26217927; https://www.reanimatology.com/rmt/article/view/2159

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    Electronic Resource

    Additional Titles: ПОСТТРАВМАТИЧЕСКИЙ ГИСТОГЕНЕЗ МЕЗОТЕЛИЯ БРЮШИНЫ В УСЛОВИЯХ РЕПАРАТИВНОЙ РЕГЕНЕРАЦИИ ПРИ СПАЕЧНОЙ БОЛЕЗНИ
    ПОСТТРАВМАТИЧНИЙ ГІСТОГЕНЕЗ МЕЗОТЕЛІЮ ОЧЕРЕВИНИ В УМОВАХ РЕПАРАТИВНОЇ РЕГЕНЕРАЦІЇ ПРИ СПАЙКОВІЙ ХВОРОБІ

    المصدر: Клінічна анатомія та оперативна хірургія; Том 16, № 4 (2017); 77-79; Клиническая анатомия и оперативная хирургия; Clinical anatomy and operative surgery; 1993-5897; 1727-0847

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