Expression of inducible nitric oxide synthase in human umbilical vein endothelial cells during primary culture

被引:42
作者
de Assis, MC
Plotkowski, MC
Fierro, IM
Barja-Fidalgo, C
de Freitas, MS [1 ]
机构
[1] Univ Estado Rio De Janeiro, Inst Biol, Dept Farmacol, BR-20551030 Rio De Janeiro, Brazil
[2] Univ Estado Rio De Janeiro, Fac Ciencias Med, Dept Microbiol & Immunol, Rio De Janeiro, Brazil
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2002年 / 7卷 / 04期
关键词
iNOS; HUVEC; primary culture; adaptive response;
D O I
10.1016/S1089-8603(02)00123-4
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
The adaptive response of endothelial cells to stress may lead to the upregulation of nitric oxide (NO) production. Herein, we report inducible nitric oxide synthase (iNOS) induction in primary cultures of human umbilical vein endothelial cells (HUVEC). The enzyme expression was earlier observed in 12-h cultures, reaching maximal levels after 3 days and decreasing when cells become confluent. The time course of NO production by HUVEC paralleled iNOS expression during the whole culture period, indicating that enzyme was functionally active. Conversely, iNOS induction could not be further detected in HUVEC subcultures passed once from cells presenting maximal levels of iNOS expression in the primary culture. Induction of iNOS in HUVEC was not related to lipopolysaccharide contamination, since the enzyme expression was not affected in the presence of polymyxin B added to primary cultures. Further analysis showed that aminoguanidine, a specific iNOS inhibitor, did not affect cell proliferation, suggesting that the NO produced by HUVEC may not be directly related to cell growth. Platelet endothelial cell adhesion molecule-1 expression was upregulated during cell confluence, in contrast to the decrease of iNOS expression and activity. The data suggest that iNOS expression may be a molecular mechanism mediating the adaptive response of endothelial cells to culture environment. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:254 / 261
页数:8
相关论文
共 47 条
[1]   ENDOCAM - A NOVEL ENDOTHELIAL-CELL CELL-ADHESION MOLECULE [J].
ALBELDA, SM ;
OLIVER, PD ;
ROMER, LH ;
BUCK, CA .
JOURNAL OF CELL BIOLOGY, 1990, 110 (04) :1227-1237
[2]  
ASSIS MC, 2000, IMMUNOLOGY, V101, P271
[3]   INDUCTION OF NO SYNTHASE IN RAT CARDIAC MICROVASCULAR ENDOTHELIAL-CELLS BY IL-1-BETA AND IFN-GAMMA [J].
BALLIGAND, JL ;
UNGUREANULONGROIS, D ;
SIMMONS, WW ;
KOBZIK, L ;
LOWENSTEIN, CJ ;
LAMAS, S ;
KELLY, RA ;
SMITH, TW ;
MICHEL, T .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 268 (03) :H1293-H1303
[4]  
Beck KF, 1999, J EXP BIOL, V202, P645
[5]   The dominant role of exogenous or endogenous interleukin-1 beta on expression and activity of inducible nitric oxide synthase in rat microvascular brain endothelial cells [J].
Bonmann, E ;
Suschek, C ;
Spranger, M ;
KolbBachofen, V .
NEUROSCIENCE LETTERS, 1997, 230 (02) :109-112
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   ISOLATION OF NITRIC-OXIDE SYNTHETASE, A CALMODULIN-REQUIRING ENZYME [J].
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (02) :682-685
[8]   Nitric oxide and its role in apoptosis [J].
Brüne, B ;
von Knethen, A ;
Sandau, KB .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 351 (03) :261-272
[9]   Endogenously produced nitric oxide inhibits endothelial cell growth as demonstrated using novel antisense cell lines [J].
Cartwright, JE ;
Johnstone, AP ;
Whitley, GS .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 131 (01) :131-137
[10]  
Cines DB, 1998, BLOOD, V91, P3527