Ka. Pritchard et al., Heat shock protein 90 mediates the balance of nitric oxide and superoxide anion from endothelial nitric-oxide synthase, J BIOL CHEM, 276(21), 2001, pp. 17621-17624
The balance of nitric oxide ( NO) and superoxide anion (O-2(radical anion))
plays an important role in vascular biology. The association of heat shock
protein 90 (Hsp90) with endothelial nitric-oxide synthase (eNOS) is a crit
ical step in the mechanisms by which eNOS generates . NO. As eNOS is capabl
e of generating both . NO and O-2(radical anion) we hypothesized that Hsp90
might also mediate eNOS-dependent O-2(.--) production. To test this hypoth
esis, bovine coronary endothelial cells (BCEC) were pretreated with geldana
mycin (GA, 10 mug/ml; 17.8 muM) and then stimulated with the calcium ionoph
ore, A23187 (5 muM). GA significantly decreased A23187-stimulated eNOS-depe
ndent nitrite production (p < 0.001, n = 4) and significantly increased A23
187-stimulated eNOS-dependent O-2(radical anion) production (p < 0.001, n =
8). A23187 increased phospho-eNOS(Ser-1179) levels by >1.6-fold over vehic
le (V)-treated levels. Pretreatment with GA by itself or with A23187 increa
sed phospho-eNOS levels. In unstimulated V-treated BCEC cultures low amount
s of Hsp90 were found to associate with eNOS. Pretreatment with GA and/or A
23187 increased the association of Hsp90 with eNOS. These data show that Hs
p90 is essential for eNOS-dependent . NO production and that inhibition of
ATP-dependent conformational changes in Hsp90 uncouples eNOS activity and i
ncreases eNOS-dependent O-2(radical anion) production.