4.7 Article

Prohibitin-1 maintains the angiogenic capacity of endothelial cells by regulating mitochondrial function and senescence

Journal

JOURNAL OF CELL BIOLOGY
Volume 180, Issue 1, Pages 101-112

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.200706072

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Funding

  1. NHLBI NIH HHS [N01-HV-28186, R01 HL064793, R01 HL 57665, N01HV28186, P01 HL 70295, R01 HL061371, R01 HL085416, 1-R01 HL 085416, R01 HL64793, R01 HL057665, R01 HL 61371, P01 HL070295] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS056206] Funding Source: Medline

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Prohibitin 1 (PHB1) is a highly conserved protein that is mainly localized to the inner mitochondrial membrane and has been implicated in regulating mitochondrial function in yeast. Because mitochondria are emerging as an important regulator of vascular homeostasis, we examined PHB1 function in endothelial cells. PHB1 is highly expressed in the vascular system and knockdown of PHB1 in endothelial cells increases mitochondrial production of reactive oxygen species via inhibition of complex I, which results in cellular senescence. As a direct consequence, both Akt and Rac1 are hyper-activated, leading to cytoskeletal rearrangements and decreased endothelial cell motility, e. g., migration and tube formation. This is also reflected in an in vivo angiogenesis assay, where silencing of PHB1 blocks the formation of functional blood vessels. Collectively, our results provide evidence that PHB1 is important for mitochondrial function and prevents reactive oxygen species-induced senescence and thereby maintains the angiogenic capacity of endothelial cells.

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