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Am J Physiol Heart Circ Physiol 292: H893-H903, 2007. First published September 29, 2006; doi:10.1152/ajpheart.00498.2006
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Nitric oxide preconditioning regulates endothelial monolayer integrity via the heat shock protein 90-soluble guanylate cyclase pathway

Galina N. Antonova,1 Connie M. Snead,1 Alexander S. Antonov,1 Christiana Dimitropoulou,2 Richard C. Venema,1,3 and John D. Catravas1,2

1Vascular Biology Center, 2Department of Pharmacology and Toxicology, and 3Department of Pediatrics, Medical College of Georgia, Augusta, Georgia

Submitted 15 May 2006 ; accepted in final form 19 September 2006

Large (pathological) amounts of nitric oxide (NO) induce cell injury, whereas low (physiological) NO concentrations often ameliorate cell injury. We tested the hypotheses that pretreatment of endothelial cells with low concentrations of NO (preconditioning) would prevent injury induced by high NO concentrations. Apoptosis, induced in bovine aortic endothelial cells (BAECs) by exposing them to either 4 mM sodium nitroprusside (SNP) or 0.5 mM N-(2-aminoethyl)-N-(2-hydroxy-2-nitrosohydrazino)-1,2-ethylenediamine (spermine NONOate) for 8 h, was abolished by 24-h pretreatment with either 100 µM SNP, 10 µM spermine NONOate, or 100 µM 8-bromo-cGMP (8-Br-cGMP). Repair of BAECs following wounding, measured as the recovery rate of transendothelial electrical resistance, was delayed by 8-h exposure to 4 mM SNP, and this delay was significantly attenuated by 24-h pretreatment with 100 µM SNP. NO preconditioning produced increased association and expression of soluble guanyl cyclase (sGC) and heat shock protein 90 (HSP90). The protective effect of NO preconditioning, but not the injurious effect of 4 mM SNP, was abolished by either a sGC activity inhibitor 1H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one (ODQ) or a HSP90 binding inhibitor (radicicol) and was mimicked by 8-Br-cGMP. We conclude that preconditioning with a low dose of NO donor accelerates repair and maintains endothelial integrity via a mechanism that includes the HSP90/sGC pathway. HSP90/sGC may thus play a role in the protective effects of NO-generating drugs from injurious stimuli.

bovine aortic endothelial cells; 8-bromoguanosine 3',5'-cyclic monophosphate; nitric oxide synthase; transendothelial electrical resistance



Address for reprint requests and other correspondence: G. Antonova, Vascular Biology Center, Medical College of Georgia, Augusta, GA, 30912-2500 (e-mail: gantonova{at}mail.mcg.edu)




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Am. J. Physiol. Heart Circ. Physiol.Home page
T. Xia, C. Dimitropoulou, J. Zeng, G. N. Antonova, C. Snead, R. C. Venema, D. Fulton, S. Qian, C. Patterson, A. Papapetropoulos, et al.
Chaperone-dependent E3 ligase CHIP ubiquitinates and mediates proteasomal degradation of soluble guanylyl cyclase
Am J Physiol Heart Circ Physiol, November 1, 2007; 293(5): H3080 - H3087.
[Abstract] [Full Text] [PDF]




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