Depletion of the ATPase NSF from Golgi membranes with hypo-S-nitrosylation of vasorelevant proteins in endothelial cells exposed to monocrotaline pyrrole

Am J Physiol Heart Circ Physiol. 2008 Nov;295(5):H1943-55. doi: 10.1152/ajpheart.00642.2008. Epub 2008 Sep 5.

Abstract

Investigations of regulated S-nitrosylation and denitrosylation of vasorelevant proteins are a newly emergent area in vascular biology. We previously showed that monocrotaline pyrrole (MCTP)-induced megalocytosis of pulmonary arterial endothelial cells (PAECs), which underlies the development of pulmonary arterial hypertension, was associated with a Golgi blockade characterized by the trapping of diverse vesicle tethers, soluble N-ethylmaleimide-sensitive factor (NSF)-attachment protein receptors (SNAREs), and soluble NSF-attachment proteins (SNAPs) in the Golgi; reduced trafficking of caveolin-1 (cav-1) and endotheial nitric oxide (NO) synthase (eNOS) from the Golgi to the plasma membrane; and decreased caveolar NO. We have investigated whether NSF, the ATPase involved in all SNARE disassembly, might be the upstream target of MCTP and whether MCTP might regulate NSF by S-nitrosylation. Immunofluorescence microscopy and Golgi purification techniques revealed the discordant decrease of NSF by approximately 50% in Golgi membranes after MCTP despite increases in alpha-SNAP, cav-1, eNOS, and syntaxin-6. The NO scavenger (4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide failed to affect the initiation or progression of MCTP megalocytosis despite a reduction of 4,5-diaminofluorescein diacetate fluorescence and inhibition of S-nitrosylation of eNOS as assayed using the biotin-switch method. Moreover, the latter assay not only revealed constitutive S-nitrosylation of NSF, eNOS, cav-1, and clathrin heavy chain (CHC) in PAECs but also a dramatic 70-95% decrease in the S-nitrosylation of NSF, eNOS, cav-1, and CHC after MCTP. These data point to depletion of NSF from Golgi membranes as a mechanism for Golgi blockade after MCTP and to denitrosylation of vasorelevant proteins as critical to the development of endothelial cell megalocytosis.

Publication types

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

MeSH terms

  • Animals
  • Blotting, Western
  • Cattle
  • Caveolin 1 / metabolism
  • Cell Fractionation
  • Cells, Cultured
  • Clathrin Heavy Chains / metabolism
  • Down-Regulation
  • Endothelial Cells / drug effects*
  • Endothelial Cells / enzymology
  • Fluorescent Antibody Technique
  • Free Radical Scavengers / pharmacology
  • Golgi Apparatus / drug effects*
  • Golgi Apparatus / enzymology
  • Monocrotaline / analogs & derivatives*
  • Monocrotaline / pharmacology
  • N-Ethylmaleimide-Sensitive Proteins / metabolism*
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type III / metabolism
  • Protein Processing, Post-Translational / drug effects*
  • Protein Transport
  • SNARE Proteins / metabolism
  • Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins / metabolism

Substances

  • Caveolin 1
  • Free Radical Scavengers
  • SNARE Proteins
  • Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins
  • Clathrin Heavy Chains
  • monocrotaline pyrrole
  • Nitric Oxide
  • Monocrotaline
  • Nitric Oxide Synthase Type III
  • N-Ethylmaleimide-Sensitive Proteins