MicroRNA-199a-3p Enhances Cardiomyocyte Hypertrophy through Targeting Retinoblastoma Transcriptional Corespressor 1
- VernacularTitle:miR-199a-3p靶向视网膜母细胞瘤转录辅阻遏子1促进心肌细胞肥大
- Author:
Jing YANG
1
;
Zhi-qin HU
2
;
Jie-ning ZHU
2
;
Hui LI
3
;
Yong-heng FU
2
;
Shu-jing YUAN
1
;
Rong PAN
1
;
Meng-zhen ZHANG
2
;
Zhi-xin SHAN
4
Author Information
1. School of Medicine,South China University of Technology,Guangzhou 510006,China
2. ResearchCenterof MedicalSciences//GuangdongCardiovascularInstitute//GuangdongGeneralHospital//GuangdongAcademyofMedical Sciences,Guangzhou510080,China
3. .SchoolofPharmacy,SouthernMedicalUniversity,Guangzhou510515,China
4. School of Medicine,South China University of Technology,Guangzhou 510006,China; ResearchCenterof MedicalSciences//GuangdongCardiovascularInstitute//GuangdongGeneralHospital//GuangdongAcademyofMedical Sciences,Guangzhou510080,China
- Publication Type:Journal Article
- Keywords:
cardiac hypertrophy;
microRNA;
miR-199a-3p;
retinoblastoma transcriptional corespressor 1
- From:
Journal of Sun Yat-sen University(Medical Sciences)
2019;40(1):23-30
- CountryChina
- Language:Chinese
-
Abstract:
【Objective】To investigate the role and the potential target of miR-199a-3p in mouse cardiac hypertrophy.【Methods】Neonatal mouse ventricular cardiomyocytes(NMVC)were isolated from the hearts of 0- 3- day- old newborn C57BL/6 mice. MiR-199a-3p mimic and retinoblastoma transcriptional corepressor 1(Rb-1)siRNA were transfected in? to NMVC to elevate the level of miR-199a-3p and inhibit Rb-1 expression,respectively. NMVC were stained with FITC- phalloidin solution to determine the size of NMVC. Dual luciferase reporter assay was performed to identify the interaction between miR- 199a- 3p and the 3’UTR of Rb- 1. mRNA and protein expression of cardiac hypertrophy associated genes were determined by RT-qPCR and Western blotting assay,respectively.【Results】(1)Over-expression of miR-199a-3pcould significantly enhance the expression of cardiac hypertrophy-related genes in NMVC ;(2)Dual-luciferase reporter assay results verified that miR- 199a-3p can interact with the 3’UTR of Rb-1. MiR-199a-3p could suppress Rb-1 ex? pression at the post-transcriptional level;(3)Functionally,miR-199a-3p mimic,consistent with Rb-1 siRNA,could increase cell size and the expression of Nppa,Acta1 and Myh7 in NMVC,and promote the nuclear translocation of E2f2 in NMVC.【Conclusions】MiR-199a-3p promotes the entry of E2f2 into the nucleus through inhibiting the expression of Rb-1,contributing to cardiomyocyte hypertrophy.