4.6 Article

The dynamics of the mitochondrial organelle as a potential therapeutic target

期刊

出版社

SAGE PUBLICATIONS INC
DOI: 10.1038/jcbfm.2012.158

关键词

Biogenesis; cerebral ischemia; mitochondrial dynamics; mitophagy; neurodegeneration

资金

  1. National Institutes of Health/NINDS [NS36736, NS43802, NS56118, NS45048]
  2. VA Merit Review Grant
  3. Chinese Natural Science Foundation [30670642, 30870794, 81020108021]
  4. VA Career Scientist Award
  5. RK Mellon Endowed Chair from the University of Pittsburgh Medical Center
  6. Changjiang Chair Professorship from the Chinese Ministry of Education
  7. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS036736, R01NS045048, R01NS056118, R01NS043802] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Mitochondria play a central role in cell fate after stressors such as ischemic brain injury. The convergence of intracellular signaling pathways on mitochondria and their release of critical factors are now recognized as a default conduit to cell death or survival. Besides the individual processes that converge on or emanate from mitochondria, a mitochondrial organellar response to changes in the cellular environment has recently been described. Whereas mitochondria have previously been perceived as a major center for cellular signaling, one can postulate that the organelle's dynamics themselves affect cell survival. This brief perspective review puts forward the concept that disruptions in mitochondrial dynamics-biogenesis, clearance, and fission/fusion events-may underlie neural diseases and thus could be targeted as neuroprotective strategies in the context of ischemic injury. To do so, we present a general overview of the current understanding of mitochondrial dynamics and regulation. We then review emerging studies that correlate mitochondrial biogenesis, mitophagy, and fission/fusion events with neurologic disease and recovery. An overview of the system as it is currently understood is presented, and current assessment strategies and their limitations are discussed. Journal of Cerebral Blood Flow & Metabolism (2013) 33, 22-32; doi:10.1038/jcbfm.2012.158; published online 24 October 2012

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