ZFYVE21 promotes endothelial nitric oxide signaling and vascular barrier function in the kidney during aging

Kidney Int. 2024 Sep;106(3):419-432. doi: 10.1016/j.kint.2024.05.007. Epub 2024 May 24.

Abstract

ZFYVE21 is an ancient, endosome-associated protein that is highly expressed in endothelial cells (ECs) but whose function(s) in vivo are undefined. Here, we identified ZFYVE21 as an essential regulator of vascular barrier function in the aging kidney. ZFYVE21 levels significantly decline in ECs in aged human and mouse kidneys. To investigate attendant effects, we generated EC-specific Zfyve21-/- reporter mice. These knockout mice developed accelerated aging phenotypes including reduced endothelial nitric oxide (ENOS) activity, failure to thrive, and kidney insufficiency. Kidneys from Zfyve21 EC-/- mice showed interstitial edema and glomerular EC injury. ZFYVE21-mediated phenotypes were not programmed developmentally as loss of ZFYVE21 in ECs during adulthood phenocopied its loss prenatally, and a nitric oxide donor normalized kidney function in adult hosts. Using live cell imaging and human kidney organ cultures, we found that in a GTPase Rab5- and protein kinase Akt-dependent manner, ZFYVE21 reduced vesicular levels of inhibitory caveolin-1 and promoted transfer of Golgi-derived ENOS to a perinuclear Rab5+ vesicular population to functionally sustain ENOS activity. Thus, our work defines a ZFYVE21- mediated trafficking mechanism sustaining ENOS activity and demonstrates the relevance of this pathway for maintaining kidney function with aging.

Keywords: ENOS; aging; endosomes; endothelial cell dysfunction.

MeSH terms

  • Aging* / metabolism
  • Aging* / physiology
  • Animals
  • Caveolin 1* / genetics
  • Caveolin 1* / metabolism
  • Endothelial Cells* / metabolism
  • Golgi Apparatus / metabolism
  • Humans
  • Kidney* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nitric Oxide Donors / pharmacology
  • Nitric Oxide Synthase Type III* / genetics
  • Nitric Oxide Synthase Type III* / metabolism
  • Nitric Oxide* / metabolism
  • Phenotype
  • Proto-Oncogene Proteins c-akt / metabolism
  • Renal Insufficiency / genetics
  • Renal Insufficiency / metabolism
  • Renal Insufficiency / physiopathology
  • Signal Transduction*
  • rab5 GTP-Binding Proteins / genetics
  • rab5 GTP-Binding Proteins / metabolism

Substances

  • CAV1 protein, human
  • Cav1 protein, mouse
  • Caveolin 1
  • Nitric Oxide
  • Nitric Oxide Donors
  • Nitric Oxide Synthase Type III
  • NOS3 protein, human
  • Nos3 protein, mouse
  • Proto-Oncogene Proteins c-akt
  • rab5 GTP-Binding Proteins