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AMPK的激活通过刺激自噬途径促进心脏分化。

Activation of AMPK promotes cardiac differentiation by stimulating the autophagy pathway.

作者信息

Kolahdouzmohammadi Mina, Pahlavan Sara, Sotoodehnejadnematalahi Fattah, Tahamtani Yaser, Totonchi Mehdi

机构信息

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.

出版信息

J Cell Commun Signal. 2023 Sep;17(3):939-955. doi: 10.1007/s12079-023-00744-z. Epub 2023 Apr 11.

Abstract

Autophagy, a critical catabolic process for cell survival against different types of stress, has a role in the differentiation of various cells, such as cardiomyocytes. Adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) is an energy-sensing protein kinase involved in the regulation of autophagy. In addition to its direct role in regulating autophagy, AMPK can also influence other cellular processes by regulating mitochondrial function, posttranslational acetylation, cardiomyocyte metabolism, mitochondrial autophagy, endoplasmic reticulum stress, and apoptosis. As AMPK is involved in the control of various cellular processes, it can influence the health and survival of cardiomyocytes. This study investigated the effects of an AMPK inducer (Metformin) and an autophagy inhibitor (Hydroxychloroquine) on the differentiation of human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs). The results showed that autophagy was upregulated during cardiac differentiation. Furthermore, AMPK activation increased the expression of CM-specific markers in hPSC-CMs. Additionally, autophagy inhibition impaired cardiomyocyte differentiation by targeting autophagosome-lysosome fusion. These results indicate the significance of autophagy in cardiomyocyte differentiation. In conclusion, AMPK might be a promising target for the regulation of cardiomyocyte generation by in vitro differentiation of pluripotent stem cells.

摘要

自噬是细胞抵御不同类型应激以维持生存的关键分解代谢过程,在各种细胞(如心肌细胞)的分化中发挥作用。5'-单磷酸腺苷(AMP)激活的蛋白激酶(AMPK)是一种参与自噬调节的能量感应蛋白激酶。除了在调节自噬中发挥直接作用外,AMPK还可通过调节线粒体功能、翻译后乙酰化、心肌细胞代谢、线粒体自噬、内质网应激和细胞凋亡来影响其他细胞过程。由于AMPK参与多种细胞过程的调控,它会影响心肌细胞的健康和存活。本研究调查了AMPK诱导剂(二甲双胍)和自噬抑制剂(羟氯喹)对人多能干细胞衍生心肌细胞(hPSC-CMs)分化的影响。结果表明,在心脏分化过程中自噬上调。此外,AMPK激活增加了hPSC-CMs中心肌细胞特异性标志物的表达。另外,自噬抑制通过靶向自噬体-溶酶体融合损害心肌细胞分化。这些结果表明自噬在心肌细胞分化中的重要性。总之,AMPK可能是通过多能干细胞体外分化来调控心肌细胞生成的一个有前景的靶点。

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