c-jun公司
细胞生物学
激酶
生物
细胞凋亡
支架蛋白
信号转导
丝裂原活化蛋白激酶
MAP激酶激酶激酶
蛋白激酶A
基因
转录因子
生物化学
作者
Michael Wilhelm,Nickolay V. Kukekov,Zhiheng Xu,Lloyd A. Greene
出处
期刊:Developmental Neuroscience
[S. Karger AG]
日期:2007-01-01
卷期号:29 (4-5): 355-362
被引量:10
摘要
The c-Jun N-terminal kinase (JNK) pathway plays an important role in neuronal apoptosis both during normal CNS development and following stroke in adult animals. As with other MAP kinase pathways, scaffold proteins regulate JNK signaling. The scaffold protein POSH (Plenty of SH3s) enhances JNK activation and apoptosis. We identified a POSH homologue, POSH2, which was cloned from rat brain and is present in cortical neurons in vitro. POSH2 mRNA is expressed in a variety of tissues including brain, and this distribution partially overlaps with that of POSH. POSH2 overexpression promotes JNK activation in HEK293 cells and promotes apoptosis in neuronal PC12 cells, which is blocked by a dominant-negative c-Jun. Finally POSH2 contains a functional RING domain and enhances the stability of coexpressed mixed-lineage kinases. These results indicate that POSH2 may regulate JNK activation and consequent apoptosis under conditions of increased expression.
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