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自噬在介导心肌细胞对铁过载的细胞反应中的重要性。

Importance of Autophagy in Mediating Cellular Responses to Iron Overload in Cardiomyocytes.

作者信息

Tam Eddie, Reno Chloe, Nguyen Khang, Cho Sungji, Sweeney Gary

机构信息

Department of Biology, York University, Toronto, ON M3J 1P3, Canada.

出版信息

Rev Cardiovasc Med. 2022 May 7;23(5):167. doi: 10.31083/j.rcm2305167. eCollection 2022 May.

Abstract

Both iron overload and deficiency can promote development of cardiomyopathy. Advances in our knowledge from recent research have indicated numerous potential cellular mechanisms. Regulation of myocardial autophagy by iron is of particular interest and will be reviewed here. Autophagy is already well established to play a significant role in regulating the development of heart failure. This review will focus on regulation of autophagy by iron, crosstalk between autophagy and other cellular process which have also already been implicated in heart failure (oxidative stress, mitochondrial dysfunction, endoplasmic reticulum stress, ferroptosis) and the therapeutic potential of targeting these interactions.

摘要

铁过载和铁缺乏均可促进心肌病的发展。近期研究使我们在认知方面取得了进展,揭示了众多潜在的细胞机制。铁对心肌自噬的调节尤其令人关注,本文将对此进行综述。自噬在调节心力衰竭发展过程中发挥重要作用已得到充分证实。本综述将聚焦于铁对自噬的调节、自噬与其他同样与心力衰竭相关的细胞过程(氧化应激、线粒体功能障碍、内质网应激、铁死亡)之间的相互作用,以及针对这些相互作用的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bd/11273664/26be1dbf76d3/2153-8174-23-5-167-g1.jpg

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