ERK MAP kinase activation is required for acetylcholine receptor inducing activity-induced increase in all five acetylcholine receptor subunit mRNAs as well as synapse-specific expression of acetylcholine receptor ε-transgene

被引:29
作者
Si, JT [1 ]
Mei, L [1 ]
机构
[1] Univ Virginia, Sch Med, Dept Pharmacol, Charlottesville, VA 22908 USA
来源
MOLECULAR BRAIN RESEARCH | 1999年 / 67卷 / 01期
关键词
ARIA; transcription; MAP kinase; synapse; acetylcholine receptor;
D O I
10.1016/S0169-328X(99)00028-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The AChR is a pentamer of four different subunits in a stoichiometry of alpha(2)beta gamma delta in embryonic and alpha(2)beta epsilon delta in adult animals. Transcription of AChR subunit genes is most active in synaptic nuclei in adult skeletal muscle cells, and is regulated by neural factors such as ARlA. We report here that ARIA up-regulated specifically the expression of all five AChR subunits in C2C12 cells. The mRNA level of erbB2, erbB3, rapsyn, MuSK, SHP-2 and beta-actin remained unchanged in response to ARIA stimulation in C2C12 cells. The ARIA-induced increase in AChR subunit expression in C2C12 cells was inhibited by the erbB kinase inhibitor tyrphostin AG1478 and the MEK inhibitor PD98059, but not by the PI3 kinase inhibitor wortmannin, suggesting an important role of the erbB protein tyrosine kinases and MAP kinase in the regulation of the expression of the five different AChR subunits. To determine the signaling pathways in vivo, we studied the expression of reporter genes driven by the epsilon-promoter in injected muscles. The in vivo expression of the epsilon-transgene was inhibited by co-expression of dominant negative mutants of key components in the MAP kinase pathway including ras, raf and MEK, but not the dominant negative mutant of PI3 kinase. These results suggest that ERK MAP kinase activation is required for ARIA-induced increase in all five AChR subunit mRNAs as well as synapse-specific expression of AChR epsilon-transgene. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:18 / 27
页数:10
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