Differential expression and function of apoptosis-associated tyrosine kinase (AATYK) in the developing mouse brain

被引:26
|
作者
Tomomura, M [1 ]
Hasegawa, Y
Hashikawa, T
Tomomura, A
Yuzaki, M
Furuichi, T
Yano, R
机构
[1] RIKEN, BSI, Lab Cellular Informat Proc, Wako, Saitama 3510198, Japan
[2] RIKEN, BSI, Mol Neurogenet Lab, Wako, Saitama 3510198, Japan
[3] RIKEN, BSI, Lab Neural Architecture, Wako, Saitama 3510198, Japan
[4] Brain Sci & Life Technol Res Fdn, Wako, Saitama, Japan
[5] Meikai Univ, Sch Dent, Dept Biochem, Sakado, Saitama 35002, Japan
[6] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
来源
MOLECULAR BRAIN RESEARCH | 2003年 / 112卷 / 1-2期
关键词
tyrosine kinase; immunohistochemistry; cerebellar granule cell; neurite outgrowth;
D O I
10.1016/S0169-328X(03)00054-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Apoptosis-associated tyrosine kinase (AATYK) is a non-receptor type tyrosine kinase that is predominantly expressed in adult mouse brain. Although it is also expressed in developing brains, its expression pattern and physiological functions are unclear. In the present study, we analyzed expression profiles of AATYK in developing mouse brains and its functional role and subcellular localization in cultured cerebellar granule cells. Expression of AATYK mRNA and protein increased during postnatal brain development. Immunohistochemical analysis indicated that the protein was differentially expressed in postmitotic neurons within various brain areas including the olfactory bulb, cerebral cortex, hippocampus, thalamus, colliculus, cerebellum, and brain stem. Developmental increases in its expression were also observed in cultured cerebellar granule cells. AATYK protein was largely fractionated into the microsomal fraction and was immunocytochemically distributed in an ER-like meshwork of the granule cell soma, suggesting a possible association with the ER membrane. AATYK protein was also present in neurites. In immature granule cells, overexpression of wild-type AATYK promoted neurite outgrowth, whereas that of tyrosine kinase-defective mutant significantly inhibited it. These results suggest that, in addition to its role in cell death in mature neurons, AATYK has a unique role in promoting neurite extension through its tyrosine kinase activity in developing neurons. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:103 / 112
页数:10
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