Sarker K P, Nakata M, Kitajima I, Nakajima T, Maruyama I
Department of Laboratory and Molecular Medicine, Faculty of Medicine, Kagoshima University, Japan.
J Mol Neurosci. 2000 Dec;15(3):243-50. doi: 10.1385/JMN:15:3:243.
Mitogen-activated protein kinase (MAPK) p38 plays pivotal role in cell proliferation, differentiation, and apoptosis when cysteine protease caspase induces apoptosis in different cell systems. SB 203580 (4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)1 H-imidazole) is widely used as a specific inhibitor of p38 MAPK, and prevents apoptosis induced by various agents. The effect of SB 203580 on nitric oxide(NO)- or peroxynitrite-induced cell death is not known. Western blotting results indicate that p38 MAPK was activated significantly in NO- or peroxynitrite-induced cell death in a time-dependent manner, and subsequently this cell death was markedly inhibited by SB 203580, as determined by fluorescence-activated cell sorting (FACS)-can analyzer. Furthermore, NO/peroxynitrite-induced caspase-3 activation was notably inhibited by SB 203580, however, phosphorylation of either p38 MAPK or p44/42 was not influenced by SB 203580. Thus, it is likely that SB 203580 prevents NO/peroxynitrite-induced cell death by inhibiting caspase-3 activation in PC-12 cells.
当半胱氨酸蛋白酶半胱天冬酶在不同细胞系统中诱导细胞凋亡时,丝裂原活化蛋白激酶(MAPK)p38在细胞增殖、分化和凋亡中起关键作用。SB 203580(4-(4-氟苯基)-2-(4-甲亚磺酰基苯基)-5-(4-吡啶基)-1H-咪唑)被广泛用作p38 MAPK的特异性抑制剂,并可防止各种因素诱导的细胞凋亡。SB 203580对一氧化氮(NO)或过氧亚硝酸盐诱导的细胞死亡的影响尚不清楚。蛋白质印迹结果表明,在NO或过氧亚硝酸盐诱导的细胞死亡中,p38 MAPK以时间依赖性方式被显著激活,随后通过荧光激活细胞分选(FACS)分析仪测定,这种细胞死亡被SB 203580显著抑制。此外,SB 203580显著抑制了NO/过氧亚硝酸盐诱导的半胱天冬酶-3激活,然而,p38 MAPK或p44/42的磷酸化不受SB 203580的影响。因此,SB 203580可能通过抑制PC-12细胞中的半胱天冬酶-3激活来防止NO/过氧亚硝酸盐诱导的细胞死亡。