TPA induces the expression of EC-SOD in human monocytic THP-1 cells: Involvement of PKC, MEK/ERK and NOX-derived ROS

被引:33
作者
Makino, Junya [1 ]
Kamiya, Tetsuro [1 ]
Hara, Hirokazu [1 ]
Adachi, Tetsuo [1 ]
机构
[1] Gifu Pharmaceut Univ, Lab Clin Pharmaceut, Gifu 5011196, Japan
关键词
extracellular-superoxide dismutase; protein kinase C; mitogen-activated protein kinase; reactive oxygen species; monocytic differentiation; EXTRACELLULAR-SUPEROXIDE-DISMUTASE; PROTEIN-KINASE-C; NF-KAPPA-B; OXIDATIVE STRESS; REACTIVE OXYGEN; U937; CELLS; COS7; SIGNAL-TRANSDUCTION; METABOLIC SYNDROME; COBALT CHLORIDE;
D O I
10.3109/10715762.2012.664841
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Extracellular-superoxide dismutase (EC-SOD) is a major SOD isozyme mainly present in the vascular wall. EC-SOD is also observed in monocytes/macrophages, and its high expression contributes to the suppression of atherosclerosis by scavenging superoxide. The molecular mechanisms governing cell-specific expression of EC-SOD are mostly unknown, while the anti-oxidative effect of EC-SOD is well recognized. In this study, we investigated the expression of EC-SOD during 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced monocytic differentiation of THP-1 cells, which is not expressing its gene in the basal phase. We confirmed the significant induction of EC-SOD in a TPA time-dependent manner, and that induction was completely blocked by pre-treatment with GF109203X, an inhibitor of protein kinase C, U0126 and PD98059, inhibitors of mitogen-activated protein kinase kinase/extracellular-signal regulated kinase. Moreover, we determined the involvement of NADPH oxidase-derived reactive oxygen species in that induction. Overall, we considered that these results may contribute to clarify the cell-specific expression of EC-SOD.
引用
收藏
页码:637 / 644
页数:8
相关论文
共 45 条
[1]
VASCULAR BOUND RECOMBINANT EXTRACELLULAR SUPEROXIDE-DISMUTASE TYPE-C PROTECTS AGAINST THE DETRIMENTAL EFFECTS OF SUPEROXIDE RADICALS ON ENDOTHELIUM-DEPENDENT ARTERIAL RELAXATION [J].
ABRAHAMSSON, T ;
BRANDT, U ;
MARKLUND, SL ;
SJOQVIST, PO .
CIRCULATION RESEARCH, 1992, 70 (02) :264-271
[2]
Reactive oxygen species mediate cyclooxygenase-2 induction during monocyte to macrophage differentiation: critical role of NADPH oxidase [J].
Barbieri, SS ;
Eligini, S ;
Brambilla, M ;
Tremoli, E ;
Colli, S .
CARDIOVASCULAR RESEARCH, 2003, 60 (01) :187-197
[3]
APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[4]
Nox proteins in signal transduction [J].
Brown, David I. ;
Griendling, Kathy K. .
FREE RADICAL BIOLOGY AND MEDICINE, 2009, 47 (09) :1239-1253
[5]
Phorbol ester-induced generation of reactive oxygen species is protein kinase Cβ-dependent and required for SAPK activation [J].
Datta, R ;
Yoshinaga, K ;
Kaneki, M ;
Pandey, P ;
Kufe, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (52) :41000-41003
[6]
Free radicals in the physiological control of cell function [J].
Dröge, W .
PHYSIOLOGICAL REVIEWS, 2002, 82 (01) :47-95
[7]
Oxidant signals and oxidative stress [J].
Finkel, T .
CURRENT OPINION IN CELL BIOLOGY, 2003, 15 (02) :247-254
[8]
FUJII J, 1991, J BIOL CHEM, V266, P23142
[9]
Increased oxidative stress in obesity and its impact on metabolic syndrome [J].
Furukawa, S ;
Fujita, T ;
Shimabukuro, M ;
Iwaki, M ;
Yamada, Y ;
Nakajima, Y ;
Nakayama, O ;
Makishima, M ;
Matsuda, M ;
Shimomura, I .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (12) :1752-1761