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G3bp1- microRNA-1 轴调节心肌细胞肥大。

G3bp1 - microRNA-1 axis regulates cardiomyocyte hypertrophy.

机构信息

From the Department of Cell Biology and Molecular Medicine, Rutgers New Jersey Medical School, Newark, NJ 07103, United States of America.

Summer undergraduate student, Rutgers University, New Brunswick, NJ, United States of America.

出版信息

Cell Signal. 2022 Mar;91:110245. doi: 10.1016/j.cellsig.2022.110245. Epub 2022 Jan 10.

Abstract

Adaptation of gene expression is one of the most fundamental response of cardiomyocytes to hypertrophic stimuli. G3bp1, an RNA binding protein with site-specific endoribonuclease activity regulates the processing of pre-miR-1 stem-loop, and thus levels of cardiomyocyte -enriched mature miR-1. Here, we examine the role of G3bp1 in regulating gene expression in quiescent cardiomyocytes and those undergoing growth-factor induced hypertrophy. Further, we determine if these changes are facilitated through G3bp1-mediated regulation of miR-1 in these cardiomyocytes. Using isolated cardiomyocytes with knockdown of endogenous G3bp1, we performed high throughput RNA sequencing to determine the change in cardiac transcriptome. Then, using gain and loss of function approach for both, G3bp1 and miR-1, alone or in combination we examine the G3bp1-miR-1 signaling in regulating gene expression and Endothelin (ET-1) -induced cardiomyocyte hypertrophy. We show that knockdown of endogenous G3bp1 results in inhibition of genes involved in calcium handling, cardiac muscle contraction, action potential and sarcomeric structure. In addition, there is inhibition of genes that contribute to hypertrophic and dilated cardiomyopathy development. Conversely, an increase is seen in genes that negatively regulate the Hippo signaling, like Rassf1 and Arrdc3, along with inflammatory genes of TGF-β and TNF pathways. Knockdown of G3bp1 restricts ET-1 induced cardiomyocyte hypertrophy. Interestingly, concurrent silencing of G3bp1 and miR-1 rescues the change in gene expression and inhibition of hypertrophy seen with knockdown of G3bp1 alone. Similarly, expression of exogenous G3bp1 reverses the miR-1 induced inhibition of gene expression. Intriguingly, expression of Gfp tagged G3bp1 results in perinuclear accumulations of G3bp1-Gfp, resembling Stress Granules. Based on our results, we conclude that G3bp1 through its regulation of mature miR-1 levels plays a critical role in regulating the expression of essential cardiac-enriched genes and those involved in development of cardiomyocyte hypertrophy.

摘要

基因表达的适应性是心肌细胞对肥大刺激的最基本反应之一。G3bp1 是一种具有特定核内核酸内切酶活性的 RNA 结合蛋白,可调节 pre-miR-1 茎环的加工,从而调节心肌细胞丰富的成熟 miR-1 的水平。在这里,我们研究了 G3bp1 在调节静止和生长因子诱导肥大的心肌细胞中的基因表达中的作用。此外,我们确定这些变化是否通过 G3bp1 介导的这些心肌细胞中 miR-1 的调节来促进。使用敲低内源性 G3bp1 的分离心肌细胞,我们进行了高通量 RNA 测序以确定心脏转录组的变化。然后,使用 G3bp1 和 miR-1 的增益和失活方法,单独或组合使用,我们研究了 G3bp1-miR-1 信号在调节基因表达和内皮素 (ET-1) 诱导的心肌细胞肥大中的作用。我们表明,敲低内源性 G3bp1 会抑制参与钙处理、心肌收缩、动作电位和肌节结构的基因。此外,还抑制了导致肥厚性和扩张型心肌病发展的基因。相反,负调节 Hippo 信号的基因(如 Rassf1 和 Arrdc3)以及 TGF-β 和 TNF 途径的炎症基因的表达增加。敲低 G3bp1 限制了 ET-1 诱导的心肌细胞肥大。有趣的是,同时沉默 G3bp1 和 miR-1 挽救了单独敲低 G3bp1 时观察到的基因表达变化和肥大抑制。同样,外源性 G3bp1 的表达逆转了 miR-1 诱导的基因表达抑制。有趣的是,表达 GFP 标记的 G3bp1 导致 G3bp1-GFP 在核周聚集,类似于应激颗粒。基于我们的结果,我们得出结论,G3bp1 通过调节成熟 miR-1 水平在调节心脏丰富基因的表达以及参与心肌细胞肥大发展的基因中发挥关键作用。

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