Inhibitors of p38 mitogen-activated protein kinase promote neuronal survival in vitro

✍ Scribed by Sonja Horstmann; Philipp J. Kahle; Gian Domenico Borasio

• Publisher: John Wiley and Sons
• Year: 1998
• Tongue: English
• Weight: 253 KB
• Volume: 52
• Category: Article
• ISSN: 0360-4012
• DOI: 10.1002/(sici)1097-4547(19980515)52:4<483::aid-jnr12>3.0.co;2-4

✦ Synopsis

Mammalian mitogen-activated protein kinases include the extracellular signal-regulated protein kinase, the c-Jun amino-terminal kinase, and the p38 subgroups. Sustained activation of Jun kinase and p38 have been shown to precede apoptosis of PC12 pheochromocytoma cells induced by withdrawal of trophic factors. To investigate the possible role of p38 in neuronal apoptosis, we tested the effect of two selective p38 inhibitors, the pyridinyl imidazole compounds SB203580 and SB202190, on different populations of chick embryonic neurons in vitro. Both substances promoted the in vitro survival of sensory, sympathetic, ciliary and motor neurons in a dosedependent fashion. When assayed in nerve growth factor-stimulated PC12 cells, SB203580 pretreatment inhibited the activation of both ribosomal S6 kinases-1 and -2 with the same IC 50 (approximately 30 M) that inhibited apoptosis in primary neurons. Thus, p38 inhibitor-sensitive pathways may be involved in apoptosis of neurotrophic factor-deprived primary neurons, and in activation of ribosomal S6 kinases.