4.7 Editorial Material

When S-Nitrosylation Gets to Mitochondria: From Signaling to Age-Related Diseases

期刊

ANTIOXIDANTS & REDOX SIGNALING
卷 32, 期 12, 页码 884-905

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/ars.2019.7872

关键词

GSNOR; metabolism; cancer; mitophagy; neurodegeneration

资金

  1. Danish Cancer Society KBVU [R146-A9414, R231-A13855]
  2. Italian Association for Cancer Research (AIRC) [IG2017-20719]
  3. NovoNordisk [2018-0052550]
  4. Tor Vergata University

向作者/读者索取更多资源

Recent Advances: Growing pieces of in vitro and in vivo evidence argue for S-nitrosylation being deeply involved in development and aging, and playing a role in the onset of different pathological states. New findings suggest it being an enzymatically regulated cellular process, with deep impact on mitochondrial structure and function, and in cellular metabolism. In light of this, the recent discovery of the denitrosylase S-nitrosoCoA (coenzyme A) reductase takes on even greater importance and opens new perspectives on S-nitrosylation as a general mechanism of cellular homeostasis. Critical Issues: Based on these recent findings, we aim at summarizing and elaborating on the established and emerging crucial roles of S-nitrosylation in mitochondrial metabolism and mitophagy, and provide an overview of the pathophysiological effects induced by its deregulation. Future Directions: The identification of new S-nitrosylation targets, and the comprehension of the mechanisms through which S-nitrosylation modulates specific classes of proteins, that is, those impinging on diverse mitochondrial functions, may help to better understand the pathophysiology of aging, and propose lines of intervention to slow down or extend the onset of aging-related diseases.

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