4.3 Review

A brief overview of BNIP3L/NIX receptor-mediated mitophagy

期刊

FEBS OPEN BIO
卷 11, 期 12, 页码 3230-3236

出版社

WILEY
DOI: 10.1002/2211-5463.13307

关键词

BNIP3L; NIX; mitochondria; mitophagy; reticulocytes

资金

  1. Croatian Science Foundation [UIP-2013-11-5246, DOK-2014-06-9538, IP-2020-02-3883]

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Mitophagy is a specialized form of autophagy that selectively removes mitochondria. BNIP3L/NIX, a well-studied mitophagy receptor, plays a crucial role in the programmed removal of healthy mitochondria across various cell types, but questions remain regarding its regulation and balancing between cellular life and death decisions.
Mitophagy is a form of autophagy specialized to selectively remove mitochondria. Although the PINK1/Parkin pathway is the best described mitophagy of damaged mitochondria, receptor/mediated mitophagy seems to have a pivotal role in cellular development and specialization. The most studied mitophagy receptor BCL2/adenovirus E1B 19-kDa-interacting protein 3-like (BNIP3L/NIX) is shown to be important for the programmed removal of healthy mitochondria during terminal differentiation of erythrocytes, but its role has been proven in various cell types. Despite recent advances in our understanding of its regulation by phosphorylation and dimerization, there remain numerous questions on how BNIP3L/NIX tightly balances between cellular life and death decisions. This brief review intends to summarize ongoing dilemmas related to BNIP3L/NIX.

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