Loss of neurons in the hippocampus and cerebral cortex of AMSH-deficient mice

被引:42
作者
Ishii, N
Owada, Y
Yamada, M
Miura, S
Murata, K
Asao, H
Kondo, H
Sugamura, K
机构
[1] Tohoku Univ, Grad Sch Med, Dept Microbiol & Immunol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Histol, Aoba Ku, Sendai, Miyagi 9808575, Japan
[3] Japan Sci & Technol Corp, CREST Program, Kawaguchi 3320012, Japan
关键词
D O I
10.1128/MCB.21.24.8626-8637.2001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
AMSH, a molecule that associates with STAM1, is involved in the in vitro cell growth signaling mediated by interleukin 2 and granulocyte-macrophage colony-stimulating factor. To investigate the in vivo functional role of AMSH, we have generated AMSH-deficient mice by gene targeting. The AMSH-deficient mice were morphologically indistinguishable from their littermates at birth, and histopathological examinations revealed normal morphogenesis in all tissues tested. However, all the AMSH-deficient mice exhibited postnatal growth retardation and died between postnatal day 19 (P19) and P23. Examination of brain sections at P6 demonstrated significant loss of neurons and apoptotic cells in the CAI subfield of the hippocampus. Brain atrophy developed by P16 and was accompanied by complete loss of the CAI neurons in the hippocampus and marked atrophy of the cerebral cortex. Furthermore, AMSH-deficient hippocampal neuronal cells were unable to survive in vitro, even in the presence of several stimulatory cytokines, while AMSH-deficient cerebellar neurons, thymocytes, and embryonic fibroblasts survived normally. Taken together, these observations indicate that AMSH is an essential molecule for the survival of neuronal cells in early postnatal mice.
引用
收藏
页码:8626 / 8637
页数:12
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