Back to Search Start Over

mi RNA-940 reduction contributes to human Tetralogy of Fallot development.

Authors :
Liang, Dandan
Xu, Xinran
Deng, Fangfei
Feng, Jing
Zhang, Hong
Liu, Ying
Zhang, Yangyang
Pan, Lei
Liu, Yi
Zhang, Dasheng
Li, Jun
Liang, Xingqun
Sun, Yunfu
Xiao, Junjie
Chen, Yi ‐ Han
Source :
Journal of Cellular & Molecular Medicine; Sep2014, Vol. 18 Issue 9, p1830-1839, 10p
Publication Year :
2014

Abstract

Tetralogy of Fallot ( TOF) is a complex congenital heart defect and the micro RNAs regulation in TOF development is largely unknown. Herein, we explored the role of mi RNAs in TOF. Among 75 dysregulated mi RNAs identified from human heart tissues, mi RNA-940 was the most down-regulated one. Interestingly, mi RNA-940 was most highly expressed in normal human right ventricular out-flow tract comparing to other heart chambers. As TOF is caused by altered proliferation, migration and/or differentiation of the progenitor cells of the secondary heart field, we isolated Sca-1<superscript>+</superscript> human cardiomyocyte progenitor cells (h CMPC) for mi RNA-940 function analysis. mi RNA-940 reduction significantly promoted h CMPCs proliferation and inhibited h CMPCs migration. We found that JARID2 is an endogenous target regulated by mi RNA-940. Functional analyses showed that JARID2 also affected h CMPCs proliferation and migration. Thus, decreased mi RNA-940 affects the proliferation and migration of the progenitor cells of the secondary heart field by targeting JARID2 and potentially leads to TOF development. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15821838
Volume :
18
Issue :
9
Database :
Complementary Index
Journal :
Journal of Cellular & Molecular Medicine
Publication Type :
Academic Journal
Accession number :
98054477
Full Text :
https://doi.org/10.1111/jcmm.12309