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自噬在心血管病理学中的作用。

The role of autophagy in cardiovascular pathology.

机构信息

Department of Molecular, Cellular and Developmental Biology, Life Sciences Institute, University of Michigan, 210 Washtenaw Ave, Ann Arbor, MI 48109-2216, USA.

Department of Biochemistry and Molecular Biology, Advanced Center for Chronic Diseases (ACCDiS), Facultad de Ciencias Químicas y Farmacéuticas & Facultad de Medicina, Universidad de Chile, Olivos 1007, Independencia, Santiago 8380492, Chile.

出版信息

Cardiovasc Res. 2022 Mar 16;118(4):934-950. doi: 10.1093/cvr/cvab158.

DOI:10.1093/cvr/cvab158
PMID:33956077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8930074/
Abstract

Macroautophagy/autophagy is a conserved catabolic recycling pathway in which cytoplasmic components are sequestered, degraded, and recycled to survive various stress conditions. Autophagy dysregulation has been observed and linked with the development and progression of several pathologies, including cardiovascular diseases, the leading cause of death in the developed world. In this review, we aim to provide a broad understanding of the different molecular factors that govern autophagy regulation and how these mechanisms are involved in the development of specific cardiovascular pathologies, including ischemic and reperfusion injury, myocardial infarction, cardiac hypertrophy, cardiac remodelling, and heart failure.

摘要

自噬是一种保守的分解代谢循环途径,其中细胞质成分被隔离、降解并回收,以在各种应激条件下存活。自噬失调已被观察到,并与几种病理学的发展和进展有关,包括心血管疾病,这是发达国家的主要死亡原因。在这篇综述中,我们旨在提供对不同分子因素的广泛理解,这些因素控制自噬的调节,以及这些机制如何参与特定心血管病理学的发展,包括缺血再灌注损伤、心肌梗死、心肌肥厚、心脏重塑和心力衰竭。

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本文引用的文献

1
Myocardial Gene Expression Signatures in Human Heart Failure With Preserved Ejection Fraction.心肌基因表达特征在射血分数保留的心力衰竭患者中。
Circulation. 2021 Jan 12;143(2):120-134. doi: 10.1161/CIRCULATIONAHA.120.050498. Epub 2020 Oct 29.
2
Structure, lipid scrambling activity and role in autophagosome formation of ATG9A.ATG9A 的结构、脂质翻转活性及其在自噬体形成中的作用。
Nat Struct Mol Biol. 2020 Dec;27(12):1194-1201. doi: 10.1038/s41594-020-00520-2. Epub 2020 Oct 26.
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Down-regulation of Beclin1 promotes direct cardiac reprogramming.Beclin1的下调促进直接心脏重编程。
Sci Transl Med. 2020 Oct 21;12(566). doi: 10.1126/scitranslmed.aay7856.
4
Fine-tuning of AMPK-ULK1-mTORC1 regulatory triangle is crucial for autophagy oscillation.微调 AMPK-ULK1-mTORC1 调节三角对自噬振荡至关重要。
Sci Rep. 2020 Oct 20;10(1):17803. doi: 10.1038/s41598-020-75030-8.
5
Defective Autophagy in Vascular Smooth Muscle Cells Alters Vascular Reactivity of the Mouse Femoral Artery.血管平滑肌细胞中自噬缺陷改变小鼠股动脉的血管反应性。
Front Physiol. 2020 Sep 23;11:548943. doi: 10.3389/fphys.2020.548943. eCollection 2020.
6
MMP9 inhibition increases autophagic flux in chronic heart failure.MMP9 抑制可增加慢性心力衰竭中的自噬通量。
Am J Physiol Heart Circ Physiol. 2020 Dec 1;319(6):H1414-H1437. doi: 10.1152/ajpheart.00032.2020. Epub 2020 Oct 16.
7
Microautophagy - distinct molecular mechanisms handle cargoes of many sizes.微自噬——不同的分子机制处理不同大小的货物。
J Cell Sci. 2020 Sep 9;133(17):jcs246322. doi: 10.1242/jcs.246322.
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Ischemia induces autophagy of endothelial cells and stimulates angiogenic effects in a hindlimb ischemia mouse model.缺血诱导内皮细胞自噬,并在小鼠后肢缺血模型中刺激血管生成作用。
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Structure of Human ATG9A, the Only Transmembrane Protein of the Core Autophagy Machinery.人类 ATG9A 的结构,核心自噬机器中唯一的跨膜蛋白。
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Novel Dual-Fluorescent Mitophagy Reporter Reveals a Reduced Mitophagy Flux in Type 1 Diabetic Mouse Heart.新型双荧光自噬报告系统揭示 1 型糖尿病小鼠心脏自噬通量降低。
J Am Osteopath Assoc. 2020 Jul 1;120(7):446-455. doi: 10.7556/jaoa.2020.072.