Abstract
ObjectiveTo explore the effect of miR-20b on apoptosis, differentiation, the BMP signaling pathway and mitochondrial function in the P19 cell model of cardiac differentiation in vitro.MethodsA miR-20b over-expression vector, a miR-20b silencing vector and their corresponding empty vectors were constructed and transfected into P19 cells, separately. Stably miR-20b overexpressing and silenced P19 cell lines were successfully selected by blasticidin and puromycin, separately. The cells were induced to undergo apoptosis in FBS-free-α-MEM. The induced cells were examined by flow cytometry and measurement of their caspase-3 activities. Quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) was used to evaluate the relative expression of marker genes of cardiomyocytes during differentiation, such as cTnT, GATA4 and ANP. QRT-PCR was also used to detect the mitochondrial DNA (mtDNA) copy number. We investigated the cellular ATP production using a luciferase-based luminescence assay. The reactive oxygen species (ROS) was determined by DCFDA (2’, 7’-Dichlorofluorescein diacetate) and the mitochondrial membrane potential (MMP) was elucidated by a JC-1 fluorescent probe, both using fluorescence microscopy and flow cytometer. The expression of BMP signaling pathway-related proteins were analyzed by Western blotting.ResultsStably miR-20b overexpressing and silenced P19 cell lines were successfully obtained. MiR-20b overexpression increased apoptosis and promoted differentiation in P19 cells by promoting the activation of the BMP signaling pathway. In addition, miR-20b overexpression induced mitochondrial impairment in P19 cells during differentiation, which was characterized by lower MMP, raised ATP synthesis and increased ROS levels. The effects of miR-20b silencing were the exact opposite to those of overexpression.ConclusionCollectively, these results suggested that miR-20b was very important in apoptosis, differentiation and mitochondrial function of P19 cells. MiR-20b may represent a new therapeutic target for congenital heart diseases and provide new insights into the mechanisms of cardiac diseases.
Highlights
The vertebrate heart is the first functional organ to form during embryonic development, and is derived from the mesodermal cells that are enriched cardiomyocytes and endocardial cells in early embryos [1]
The effects of miR-20b silencing were the exact opposite to those of overexpression. These results suggested that miR-20b was very important in apoptosis, differentiation and mitochondrial function of P19 cells
We explored the effects of miR-20b on apoptosis, differentiation, Bone morphogenetic proteins (BMPs) signaling pathway and mitochondrial function in the P19 cell model of cardiac differentiation in vitro
Summary
The vertebrate heart is the first functional organ to form during embryonic development, and is derived from the mesodermal cells that are enriched cardiomyocytes and endocardial cells in early embryos [1]. The formation of a mature healthy heart, having four chambers, relies on the sequential expression of many genes, a variety of signaling pathways, such as the BMP signaling pathway, the Wnt signaling pathway, and a series of important morphological changes, including cell migration and differentiation [2,3]. Many studies have shown that cardiac malformation occurs if mutations or deletions exist in any part of the above procedures [4,5,6], with a prevalence of approximately eight in every 1000 newborn infants [7], which places a heavy burden on families and society. The majority of CHDs are related to gene deletions and mutations [9,10]. Genetic studies are the key to the prevention and treatment of CHDs
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