Influence of MicroRNA-382 on Biological Properties of Human Umbilical Cord-Derived Mesenchymal Stem Cells.
- Author:
Jun-Jie CUI
1
;
Ying CHI
1
;
Xin YANG
1
;
Yu-Yan SHEN
1
;
Zhao WANG
1
;
Su-Dong ZHANG
1
;
Li-Ning ZHANG
1
;
Li LIU
1
;
Shi-Hong LU
1
;
Ming-Zhe HAN
1
;
Si-Zhou FENG
2
Author Information
- Publication Type:Journal Article
- MeSH: Cell Differentiation; Core Binding Factor Alpha 1 Subunit; metabolism; Granulocyte Colony-Stimulating Factor; metabolism; Granulocyte-Macrophage Colony-Stimulating Factor; metabolism; Humans; Indoleamine-Pyrrole 2,3,-Dioxygenase; metabolism; Interleukin-6; metabolism; Macrophage Colony-Stimulating Factor; metabolism; Mesenchymal Stromal Cells; cytology; MicroRNAs; metabolism; Osteogenesis; Transfection; Umbilical Cord; cytology
- From: Journal of Experimental Hematology 2016;24(3):852-857
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the effect of microRNA-382 (miR-382) on the biological properties of human umbilical cord-derived mesenchymal stem cells (hUC-MSC).
METHODSThe mimics and inhibitor of miR-382 were transfected into hUC-MSC with lipo2000. Inverted microscopy was used to observe the morphology change of hUC-MSC. The proliferation of hUC-MSC was detected by CCK-8. Oil red O and alizarin red staining were applied to assess the adipogenic and osteogenic differentiation of hUC-MSC. Cetylpyridinium chloride was used to the quantitative analysis of osteogenic differentiation. The expression of Runx2 and some cytokines were detected by RT-PCR.
RESULTSmiR-382 did not influence the morphology, proliferation and adipogenic differentiation of hUC-MSC miR-382 inhibited the expression of Runx2, thus could inhibit the osteogenesis of hUC-MSC, being confirmed by alizarin red stain; miR-382 could influence the expression of key cytokines secreted from hUC-MSC, such as IL-6, IDO1, G-CSF, M-CSF, GM-CSF.
CONCLUSIONmiR-382 decreases the expression of Runx2 and inhibites the osteogenesis of hUC-MSC. In addition, it also affects the expression of some key cytokines secreted from hUC-MSC.