Neuronal differentiation of neuro 2a cells by inhibitors of cell cycle progression, trichostatin A and butyrolactone I
Authors
Inokoshi, J
Katagiri, M
Arima, S
Tanaka, H
Hayashi, M
Kim, YB
Furumai, R
Yoshida, M
Horinouchi, S
Omura, S
Citation
J. Inokoshi et al., Neuronal differentiation of neuro 2a cells by inhibitors of cell cycle progression, trichostatin A and butyrolactone I, BIOC BIOP R, 256(2), 1999, pp. 372-376
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
SICI code
0006-291X(19990316)256:2<372:NDON2C>2.0.ZU;2-Z
Abstract
Trichostatin A (TSA, 17 nM), a specific and reversible inhibitor of histone
deacetylase induced neurite network formation at and after 4 days. The net
works were preserved for at least 3 weeks in the presence of TSA. Butyrolac
tone I (BLI, 23.6 mu M), an inhibitor of cdc2 and cdk2 kinases, also induce
d neurite extension. Both compounds enhanced the acetylcholinesterase activ
ity of the cells. Cell cycle progression of the cells was blocked by TSA (1
7 nM) at G1 phase alone. Furthermore, the level of histone hyperacetylation
and p21(WAF1) expression in TSA-treated cells increased transiently. These
findings suggest that the induction of the neuronal differentiation in Neu
ro 2a cells by these agents requires the cell cycle arrest at G1 phase, whi
ch is caused by inhibition of cycline dependent kinase, a target molecule o
f BLI and p21(WAF1). (C) 1999 Academic Press.