Modulation of vascular ATP diphosphohydrolase by fatty acids

被引:25
作者
Robson, SC
Daoud, S
Begin, M
Cote, YP
Siegel, JB
Bach, FH
Beaudoin, AR
机构
[1] UNIV SHERBROOKE,FAC SCI,DEPT BIOL,SHERBROOKE,PQ J1K 2R1,CANADA
[2] NEW ENGLAND DEACONESS HOSP,DEPT SURG,SANDOZ CTR IMMUNOBIOL,BOSTON,MA 02215
关键词
ATPDase; cell membrane; endothelium; vascular; fatty acids; lipid peroxides; membrane lipids; oxygen;
D O I
10.1097/00001721-199701000-00005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Endothelial cells (EC) possess several protective thromboregulatory mechanisms that may be perturbed by cell activation or injury. Vascular ATP-diphosphohydrolase (ATPDase) has been demonstrated on both aortic EC and smooth muscle cells and may play a key regulatory role in hemostasis and platelet reactivity by converting extracellular ATP and ADP to AMP. We have examined the role of exogenous saturated or unsaturated fatty acids in the modulation of EC associated ATPDase activity in vitro. EC growth was not dramatically influenced by supplementation with fatty acids whereas viability was enhanced by oleic, butyrate and eicosapentaenoic acid. EC cultures supplemented with saturated or a monounsaturated (oleic acid) fatty acid(s) had markedly increased ATPDase activity, whereas those exposed to polyunsaturated fatty acids showed substantive decreases. Exogenous oleic acid could also protect against the significant loss of ATPDase activity, following exposure to reactive oxygen intermediates in vitro. We conclude that endothelial ATPDase activity may be regulated by exogenous fatty acids and that underlying mechanisms include alterations in the nature of the phospholipid composition of EC membranes that influence responses to oxidative stress reactions.
引用
收藏
页码:21 / 27
页数:7
相关论文
共 28 条
[1]   METABOLISM OF EXTRACELLULAR ADENINE-NUCLEOTIDES BY HUMAN ENDOTHELIAL-CELLS EXPOSED TO REACTIVE OXYGEN METABOLITES [J].
AALTO, TK ;
RAIVIO, KO .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (02) :C282-C286
[2]   OXYGEN RADICALS INHIBIT HUMAN PLASMA ACETYLHYDROLASE, THE ENZYME THAT CATABOLIZES PLATELET-ACTIVATING-FACTOR [J].
AMBROSIO, G ;
ORIENTE, A ;
NAPOLI, C ;
PALUMBO, G ;
CHIARIELLO, P ;
MARONE, G ;
CONDORELLI, M ;
CHIARIELLO, M ;
TRIGGIANI, M .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (06) :2408-2416
[3]   PLATELETS AND ECTONUCLEOTIDASES [J].
BAKKER, WW ;
POELSTRA, K ;
BARRADAS, MA ;
MIKHAILIDIS, DP .
PLATELETS, 1994, 5 (03) :121-129
[4]  
BARRADAS M R, 1987, Diabetes Research and Clinical Practice, V3, P9, DOI 10.1016/S0168-8227(87)80003-7
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   THE EFFECT OF A FISH OIL ENRICHED DIET ON OXYGEN-TOXICITY AND LIPID-PEROXIDATION IN MICE [J].
BURNS, A ;
LIN, YG ;
GIBSON, R ;
JAMIESON, D .
BIOCHEMICAL PHARMACOLOGY, 1991, 42 (07) :1353-1360
[7]   IDENTIFICATION AND LOCALIZATION OF ATP-DIPHOSPHOHYDROLASE (APYRASE) IN BOVINE AORTA - RELEVANCE TO VASCULAR TONE AND PLATELET-AGGREGATION [J].
COTE, YP ;
PICHER, M ;
STJEAN, P ;
BELIVEAU, R ;
POTIER, M ;
BEAUDOIN, AR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1078 (02) :187-191
[8]   CHARACTERIZATION OF ATP-DIPHOSPHOHYDROLASE ACTIVITIES IN THE INTIMA AND MEDIA OF THE BOVINE AORTA - EVIDENCE FOR A REGULATORY ROLE IN PLATELET ACTIVATION INVITRO [J].
COTE, YP ;
FILEP, JG ;
BATTISTINI, B ;
GAUVREAU, J ;
SIROIS, P ;
BEAUDOIN, AR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1139 (1-2) :133-142
[9]  
Freshney R.A., 1987, CULTURE ANIMAL CELLS, VSecond
[10]   A MALACHITE GREEN COLORIMETRIC ASSAY FOR PROTEIN PHOSPHATASE-ACTIVITY [J].
GELADOPOULOS, TP ;
SOTIROUDIS, TG ;
EVANGELOPOULOS, AE .
ANALYTICAL BIOCHEMISTRY, 1991, 192 (01) :112-116