The Jnk1 and Jnk2 protein kinases are required for regional specific apoptosis during early brain development

被引:771
作者
Kuan, CY
Yang, DD
Roy, DRS
Davis, RJ [1 ]
Rakic, P
Flavell, RA
机构
[1] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Biochem & Mol Biol, Worcester, MA 01605 USA
[3] Yale Univ, Sch Med, Howard Hughes Med Inst, Immunobiol Sect, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Neurobiol Sect, New Haven, CT 06510 USA
关键词
D O I
10.1016/S0896-6273(00)80727-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The c-Jun NH2-terminal kinase (Jnk) family is implicated in apoptosis, but its function in brain development is unclear. Here, we address this issue using mutant mice lacking different members of the family (Jnk1, Jnk2, and Jnk3). Mice deficient in Jnk1, Jnk2, Jnk3, and Jnk1/Jnk3 or Jnk2/Jnk3 double mutants all survived normally. Compound mutants lacking Jnk1 and Jnk2 genes were embryonic lethal and had severe dysregulation of apoptosis in brain. Specifically, there was a reduction of cell death in the lateral edges of hindbrain prior to neural tube closure. In contrast, increased apoptosis and caspase activation were found in the mutant forebrain, leading to precocious degeneration. These results suggest that Jnk1 and Jnk2 regulate region-specific apoptosis during early brain development.
引用
收藏
页码:667 / 676
页数:10
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