eNOS phosphorylation in health and disease

被引:158
作者
Kolluru, Gopi Krishna [1 ]
Siamwala, Jamila H. [1 ]
Chatterjee, Suvro [1 ]
机构
[1] Anna Univ, Vasc Biol Lab, AU KBC Res Ctr, Madras 600044, Tamil Nadu, India
关键词
eNOS; Serine phosphorylation; Nitric oxide; NITRIC-OXIDE SYNTHASE; DEPENDENT DIABETES-MELLITUS; ENDOTHELIAL NO SYNTHASE; FLUID SHEAR-STRESS; C-REACTIVE PROTEIN; CALCIUM-INDEPENDENT ACTIVATION; PERIPHERAL ARTERIAL-DISEASE; VASCULAR OXIDATIVE STRESS; SOLUBLE GUANYLYL CYCLASE; HIGH-FAT DIET;
D O I
10.1016/j.biochi.2010.03.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endothelium plays a fundamental role in maintaining the vascular tone by releasing various biochemical factors that modulate the contractile and relaxatory behavior of the underlying vascular smooth muscle, regulation of inflammation, immunomodulation, platelet aggregation, and thrombosis. Endothelium regulates these cellular processes by activating endothelial nitric oxide synthase (eNOS) responsible for nitric oxide (NO) production. eNOS is constitutively expressed in ECs in response to humoral, mechanical or pharmacological stimulus. eNOS activity is regulated mainly by protein-protein interactions and multisite phosphorylations. The phosphorylation state of specific serine, threonine and tyrosine residues of the enzyme plays a pivotal role in regulation of eNOS activity. Perturbations of eNOS phosphorylation have been reported in a number of diseases thereby emphasizing the importance of regulation of eNOS activity. This review summarizes the mechanism of eNOS regulation through multi-site phosphorylation in different pathologies. Attempts have been made to highlight phosphorylation of eNOS at various residues, regulation of the enzyme activity via posttranslational modifications and its implications on health and disease. (C) 2010 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1186 / 1198
页数:13
相关论文
共 237 条
[121]   NITRIC-OXIDE SYNTHASE - ASPECTS CONCERNING STRUCTURE AND CATALYSIS [J].
MARLETTA, MA .
CELL, 1994, 78 (06) :927-930
[122]   Upregulation of endothelial constitutive NOS: A major role in the increased NO production in cirrhotic rats [J].
Martin, PY ;
Xu, DL ;
Niederberger, M ;
Weigert, A ;
Tsai, P ;
StJohn, J ;
Gines, P ;
Schrier, RW .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1996, 270 (03) :F494-F499
[123]   Nitric oxide-generating hydrogels inhibit neointima formation [J].
Masters, KSB ;
Lipke, EA ;
Rice, EEH ;
Liel, MS ;
Myler, HA ;
Zygourakis, C ;
Tulis, DA ;
West, JL .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2005, 16 (05) :659-672
[124]   Enhanced electron flux and reduced calmodulin dissociation may explain "calcium-independent" eNOS activation by phosphorylation [J].
McCabe, TJ ;
Fulton, D ;
Roman, LJ ;
Sessa, WC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) :6123-6128
[125]  
MCVEIGH GE, 1992, DIABETOLOGIA, V35, P771
[126]   ENDOTHELIUM-DEPENDENT RELAXATION IN AORTA OF BB RAT [J].
MERAJI, S ;
JAYAKODY, L ;
SENARATNE, MPJ ;
THOMSON, ABR ;
KAPPAGODA, T .
DIABETES, 1987, 36 (08) :978-981
[127]   Reciprocal regulation of endothelial nitric-oxide synthase by Ca2+-calmodulin and caveolin [J].
Michel, JB ;
Feron, O ;
Sacks, D ;
Michel, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (25) :15583-15586
[128]   Nitric oxide synthases: Which, where, how, and why? [J].
Michel, T ;
Feron, O .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (09) :2146-2152
[129]   PHOSPHORYLATION AND SUBCELLULAR TRANSLOCATION OF ENDOTHELIAL NITRIC-OXIDE SYNTHASE [J].
MICHEL, T ;
LI, GK ;
BUSCONI, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (13) :6252-6256
[130]   Coordinated control of endothelial nitric-oxide synthase phosphorylation by protein kinase C and the cAMP-dependent protein kinase [J].
Michell, BJ ;
Chen, ZP ;
Tiganis, T ;
Stapleton, D ;
Katsis, F ;
Power, DA ;
Sim, AT ;
Kemp, BE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (21) :17625-17628