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Suppression of miR-181 a attenuates H2O2-induced death of mesenchymal stem cells by maintaining hexokinase II expression

Authors :
Seahyoung Lee
Ina Yun
Onju Ham
Se-Yeon Lee
Chang Yeon Lee
Jun-Hee Park
Jiyun Lee
Hyang-Hee Seo
Eunhyun Choi
Ki-Chul Hwang
Source :
Biological Research, Vol 48, Iss 0, Pp 1-7 (2015)
Publication Year :
2015
Publisher :
BMC, 2015.

Abstract

BACKGROUND: Low survival rate of transplanted cells compromises the efficacy of cell therapy. Hexokinase II (HKII) is known to have anti-apoptotic activity through its interaction with mitochondria. The objective was to identify miRNAs targeting HKII and investigate whether miRNA-mediated modulation of HKII could improve the survival of mesenchymal stem cells (MSCs) exposed to H2O2. The expression of HKII in MSCs exposed to H2O2 was evaluated, and HKII-targeting miRNA was screened based on miRNA-target prediction databases. The effect of H2O2 on the expression of the selected HKII-targeting miRNA was examined and the effect of modulation of the selected HKII-targeting miRNA using anti-miRNA on H2O2-induced apoptosis of MSC was evaluated. RESULTS: H2O2 (600 μΜ) induced cell death of MSCs and decreased mitochondrial HKII expression. We have identified miR-181a as a HKII-targeting miRNA and H2O2 increased the expression of miR-181a in MSCs. Delivery of anti-miR-181a, which neutralizes endogenous miR-181a, significantly attenuated H2O2-induced decrease of HKII expression and disruption of mitochondrial membrane potential, improving the survival of MSCs exposed to H2O2. CONCLUSIONS: These findings suggest that H2O2-induced up-regulation of miR-181a contributes to the cell death of MSCs by down-regulating HKII. Neutralizing miR-181a can be an effective way to prime MSCs for transplantation into ischemic tissues.

Details

Language :
English
ISSN :
07169760
Volume :
48
Issue :
0
Database :
Directory of Open Access Journals
Journal :
Biological Research
Publication Type :
Academic Journal
Accession number :
edsdoj.98e66a83ab124672ac654a64a367f8a2
Document Type :
article
Full Text :
https://doi.org/10.1186/S40659-015-0036-5