4.6 Review

Mending a broken heart: the role of mitophagy in cardioprotection

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00708.2014

关键词

autophagy; mitophagy; mitochondria; parkin; BNIP3; FUNDC1

资金

  1. National Institutes of Health [HL-087023, HL-101217, HL-085577, HL-67724, HL-91469, HL-102738, HL-112330, AG-23039, T32HL-007444]
  2. Fondation Leducq Transatlantic Networks of Excellence
  3. American Heart Association Established Investigator Award [14EIA18970095]

向作者/读者索取更多资源

The heart is highly energy dependent with most of its energy provided by mitochondrial oxidative phosphorylation. Mitochondria also play a role in many other essential cellular processes including metabolite synthesis and calcium storage. Therefore, maintaining a functional population of mitochondria is critical for cardiac function. Efficient degradation and replacement of dysfunctional mitochondria ensures cell survival, particularly in terminally differentiated cells such as cardiac myocytes. Mitochondria are eliminated via mitochondrial autophagy or mitophagy. In the heart, mitophagy is an essential housekeeping process and required for cardiac homeostasis. Reduced autophagy and accumulation of impaired mitochondria have been linked to progression of heart failure and aging. In this review, we discuss the pathways that regulate mitophagy in cells and highlight the cardioprotective role of mitophagy in response to stress and aging. We also discuss the therapeutic potential of targeting mitophagy and directions for future investigation.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据