Mesenchymal Stem Cells Were Affected by Up-regulation of MiRNA-21 in Vitro
Overview
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Background: The expression of miRNA-21 was high in cells that were derived from MSCs, but, the role of miRNA-21in the MSCs was unknown.
Material/methods: In this study, flow cytometry, which was used to identify the surface-associated antigens of MSCs. The 10 μmol/l 5-azacytidine was used to induce MSCs to differentiate to cardiomyocyte-like cells. Immunofluorescence, that was for detected the expression of troponin I (cTnI). The samples were assigned to 3 groups: the blank group, the miRNA-21 mimic group, and the negative control (NC) group. The proliferation of MSCs was detected by methyl thiazolylte-trazolium (MTT), the apoptosis of MSCs was analyzed by flow cytometry, Western-blot, which was used to identify the expression of cTNI and myoD in the MSCs.
Results: The proliferation of MSCs was increased, because of the over expression of miRNA-21; But, the apoptotic rate of the MSCs were slower in MIRNA-21 group, on account of the expression of miRNA-21 was higher than that of in the NC and CK groups. The expression of cTNI in miRNA-21 group was higher than that of in the NC and CK groups.
Conclusions: The results also suggested that, the up-regulation of miRNA-21 enhanced proliferation of MSCs, reducing the apoptosis of MSCs. MiRNA-21 promotes the differentiation of MSCs, which may pave the way for the treatment directed toward restoring miRNA-21 function for myocardial ischemia.
Yang W, Zhao L, Xue S, Liu J, Shan J Arch Med Sci. 2022; 18(6):1672-1677.
PMID: 36457985 PMC: 9710289. DOI: 10.5114/aoms/154956.
MicroRNA Regulation of Bone Marrow Mesenchymal Stem Cell Chondrogenesis: Toward Articular Cartilage.
Vail D, Somoza R, Caplan A Tissue Eng Part A. 2021; 28(5-6):254-269.
PMID: 34328786 PMC: 8971999. DOI: 10.1089/ten.TEA.2021.0112.