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Cardiolipin-targeted peptides rejuvenate mitochondrial function, remodel mitochondria, and promote tissue regeneration during aging

期刊

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
卷 660, 期 -, 页码 137-148

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2018.10.013

关键词

Szeto-schiller peptides; SS-31; Mitochondrial cristae; Mitochondrial dynamics; Respiratory supercomplexes

资金

  1. National Institute on Aging [P01 AG001751]
  2. Social Profit Network
  3. NATIONAL INSTITUTE ON AGING [P01AG001751] Funding Source: NIH RePORTER

向作者/读者索取更多资源

It has been proposed that a loss of bioenergetic capacity of cells contributes to the progressive loss of biological function with age. Aging is associated with loss of mitochondrial cristae membranes and inhibition of ATP production. Despite the many approaches being pursued for improving mitochondrial function, none of them directly targets the electron transport chain to improve ATP production. Recent studies have brought attention to cardiolipin as a unique target for promoting mitochondrial efficiency. Cardiolipin is important for cristae curvatures and is necessary for optimal activity of the respiratory complexes and the assembly of supercomplexes. Here we describe the discovery of a class of cell-penetrating aromatic-cationic tetrapeptides that selectively target cardiolipin and increase coupling efficiency while reducing reactive oxygen species production. These compounds can rejuvenate mitochondrial bioenergetics, remodel mitochondrial cristae structure, repair cellular structure, and restore organ function during aging.

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