The scavenger receptor class B type I adaptor protein PDZK1 maintains endothelial monolayer integrity

Circ Res. 2008 Feb 29;102(4):480-7. doi: 10.1161/CIRCRESAHA.107.159079. Epub 2008 Jan 3.

Abstract

Circulating levels of high-density lipoprotein (HDL) cholesterol are inversely related to the risk of cardiovascular disease, and HDL and the HDL receptor scavenger receptor class B type I (SR-BI) initiate signaling in endothelium through src that promotes endothelial NO synthase activity and cell migration. Such signaling requires the C-terminal PDZ-interacting domain of SR-BI. Here we show that the PDZ domain-containing protein PDZK1 is expressed in endothelium and required for HDL activation of endothelial NO synthase and cell migration; in contrast, endothelial cell responses to other stimuli, including vascular endothelial growth factor, are PDZK1-independent. Coimmunoprecipitation experiments reveal that Src interacts with SR-BI, and this process is PDZK1-independent. PDZK1 also does not regulate SR-BI abundance or plasma membrane localization in endothelium or HDL binding or cholesterol efflux. Alternatively, PDZK1 is required for HDL/SR-BI to induce Src phosphorylation. Paralleling the in vitro findings, carotid artery reendothelialization following perivascular electric injury is absent in PDZK1-/- mice, and this phenotype persists in PDZK1-/- mice with genetic reconstitution of PDZK1 expression in liver, where PDZK1 modifies SR-BI abundance. Thus, PDZK1 is uniquely required for HDL/SR-BI signaling in endothelium, and through these mechanisms, it is critically involved in the maintenance of endothelial monolayer integrity.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta / cytology
  • Cattle
  • Cell Movement / physiology
  • Cells, Cultured
  • Endothelial Cells / cytology*
  • Endothelial Cells / metabolism*
  • Enzyme Activation / physiology
  • Lipoproteins, HDL / metabolism*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Mutant Strains
  • Nitric Oxide Synthase Type II / metabolism
  • Nitric Oxide Synthase Type III
  • STAT1 Transcription Factor / physiology
  • Scavenger Receptors, Class B / metabolism*
  • Tunica Intima / cytology
  • Tunica Intima / metabolism

Substances

  • Lipoproteins, HDL
  • Membrane Proteins
  • Pdzk1ip1 protein, mouse
  • STAT1 Transcription Factor
  • Scarb1 protein, mouse
  • Scavenger Receptors, Class B
  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III
  • Nos3 protein, mouse