An eIF3a gene mutation dysregulates myocardium growth with left ventricular noncompaction via the p-ERK1/2 pathway
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An eIF3a gene mutation dysregulates myocardium growth with left ventricular noncompaction via the p-ERK1/2 pathway
Genes & DiseasesVol. 8, Issue 4, (2021)
作者机构:
1. Department of Cardiology, Children's Hospital of Chongqing Medical University,Chongqing,PR China,401122
2. China International Science and Technology Cooperation Center for Child Development and Critical Disorders, Chongqing Key Laboratory of Pediatrics, Ministry of Education Key Laboratory of Child Development and Disorders,Chongqing,PR China,401122
Mei Ge, Xuehan Bai, Aoyi Liu, et al. An eIF3a gene mutation dysregulates myocardium growth with left ventricular noncompaction via the p-ERK1/2 pathway. [J]. Genes & Diseases 8(4).(2021)
DOI:
Mei Ge, Xuehan Bai, Aoyi Liu, et al. An eIF3a gene mutation dysregulates myocardium growth with left ventricular noncompaction via the p-ERK1/2 pathway. [J]. Genes & Diseases 8(4).(2021) DOI: 10.1016/j.gendis.2020.02.003.
An eIF3a gene mutation dysregulates myocardium growth with left ventricular noncompaction via the p-ERK1/2 pathway
摘要
Abstract
Left ventricular noncompaction (LVNC) is a heterogeneous disorder with unclear genetic causes and an unknown mechanism. eIF3a
an important member of the Eukaryotic translation initiation factor 3 (eIF3) family
is involved in multiple biological processes
including cell proliferation and migration during myocardial development
suggesting it could play a role in LVNC development. To investigate the association between a novel variant (c.1145 A-
>
G) in eIF3a and LVNC
and explore potential mechanisms that could lead to the development of LVNC. A novel eIF3a variant
c.1145 A-
>
G
was identified by whole-exome sequencing in a familial pedigree with LVNC. Adenovirus vectors containing wild-type eIF3a and the mutated version were constructed and co-infected into H9C2 cells. Cell proliferation
apoptosis
cell migration
and differentiation
as well as phosphorylation of ERK1/2 were studied and were measured by proliferation assays
flow cytometry
real-time PCR and Western blot
respectively. The eIF3a mutation inhibited the proliferation of H9C2 cells
induced apoptosis
promoted cell migration
and inhibited the differentiation of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs). The effect of the eIF3a mutation may be attributed to a decrease in expression of p-ERK1/2. A novel
eIF3a
gene mutation disrupted the p-ERK1/2 pathway and caused decreased myocardium proliferation
differentiation
accelerated migration.This finding may provide some insight into the mechanism involved in LVNC development.
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Related Institution
Department of Cell Biology, Army Medical University
Department of Pediatric Surgery, The Children’s Hospital of Chongqing Medical University
Stem Cell Biology and Therapy Laboratory, The Children’s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics
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