The regulation of endothelial nitric oxide synthase by caveolin: a paradigm validated in vivo and shared by the 'endothelium-derived hyperpolarizing factor'

被引:34
作者
Dessy, Chantal [1 ]
Feron, Olivier [1 ]
Balligand, Jean-Luc [1 ]
机构
[1] Catholic Univ Louvain, Inst Expt & Clin Res, B-1200 Brussels, Belgium
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2010年 / 459卷 / 06期
关键词
Endothelium; Nitric oxide; Caveolae; Caveolin; EDHF; INDUCED PULMONARY-HYPERTENSION; BLOOD-PRESSURE VARIABILITY; KNOCKOUT MICE; SIGNAL-TRANSDUCTION; CARDIAC MYOCYTES; NAD(P)H OXIDASE; NO SYNTHASE; HEART-RATE; NULL-MICE; ACTIVATION;
D O I
10.1007/s00424-010-0815-3
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
The endothelium plays a crucial role in the regulation of cardiovascular homeostasis through the release of vasoactive autacoids such as nitric oxide, prostacyclin, and a third factor or pathway termed 'endothelium-derived hyperpolarizing factor' (EDHF). Although the functional influence of NO and EDHF is sometimes reciprocal (i.e., their effects decrease or increase with the reduction in vessel diameter, respectively), recent insights led to the identification of caveolae and caveolin as common regulators of their production. In this review, we will first focus on the current understanding of the caveolin/eNOS paradigm and will then detail the most recent findings on the role of caveolae in driving EDHF-signaling pathways.
引用
收藏
页码:817 / 827
页数:11
相关论文
共 68 条
[1]
Effects of methyl β-cyclodextrin on EDHF responses in pig and rat arteries; association between SKCa channels and caveolin-rich domains [J].
Absi, M. ;
Burnham, M. P. ;
Weston, A. H. ;
Harno, E. ;
Rogers, M. ;
Edwards, G. .
BRITISH JOURNAL OF PHARMACOLOGY, 2007, 151 (03) :332-340
[2]
Ambudkar Indu S, 2004, Novartis Found Symp, V258, P63
[3]
Caveolin-1 contributes to assembly of store-operated Ca2+ influx channels by regulating plasma membrane localization of TRPC1 [J].
Brazer, SCW ;
Singh, BB ;
Liu, XB ;
Swaim, W ;
Ambudkar, IS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (29) :27208-27215
[4]
Antitumor effects of in vivo caveolin gene delivery are associated with the inhibition of the proangiogenic and vasodilatory effects of nitric oxide [J].
Brouet, A ;
DeWever, J ;
Martinive, P ;
Havaux, X ;
Bouzin, C ;
Sonveaux, P ;
Feron, O .
FASEB JOURNAL, 2004, 18 (15) :602-+
[5]
Hsp90 ensures the transition from the early Ca2+-dependent to the late phosphorylation-dependent activation of the endothelial nitric-oxide synthase in vascular endothelial growth factor-exposed endothelial cells [J].
Brouet, A ;
Sonveaux, P ;
Dessy, C ;
Balligand, JL ;
Feron, O .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (35) :32663-32669
[6]
Hsp90 and caveolin are key targets for the proangiogenic nitric oxide-mediated effects of statins [J].
Brouet, A ;
Sonveaux, P ;
Dessy, C ;
Moniotte, S ;
Balligand, JL ;
Feron, O .
CIRCULATION RESEARCH, 2001, 89 (10) :866-873
[7]
In vivo delivery of the caveolin-1 scaffolding domain inhibits nitric oxide synthesis and reduces inflammation [J].
Bucci, M ;
Gratton, JP ;
Rudic, RD ;
Acevedo, L ;
Roviezzo, F ;
Cirino, G ;
Sessa, WC .
NATURE MEDICINE, 2000, 6 (12) :1362-1367
[8]
NAD(P)H oxidase-derived hydrogen peroxide mediates endothelial nitric oxide production in response to angiotensin [J].
Cai, H ;
Li, ZM ;
Dikalov, S ;
Holland, SM ;
Hwang, JN ;
Jo, H ;
Dudley, SC ;
Harrison, DG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (50) :48311-48317
[9]
PURIFICATION AND CHARACTERIZATION OF SMOOTH-MUSCLE CELL CAVEOLAE [J].
CHANG, WJ ;
YING, YS ;
ROTHBERG, KG ;
HOOPER, NM ;
TURNER, AJ ;
GAMBLIEL, HA ;
DEGUNZBURG, J ;
MUMBY, SM ;
GILMAN, AG ;
ANDERSON, RGW .
JOURNAL OF CELL BIOLOGY, 1994, 126 (01) :127-138
[10]
Increased neuronal nitric oxide synthase-derived NO production in the failing human heart [J].
Damy, T ;
Ratajczak, P ;
Shah, AM ;
Camors, E ;
Marty, I ;
Hasenfuss, G ;
Marotte, F ;
Samuel, JL ;
Heymes, C .
LANCET, 2004, 363 (9418) :1365-1367