TY - JOUR
T1 - Differential expression and function of apoptosis-associated tyrosine kinase (AATYK) in the developing mouse brain
AU - Tomomura, Mineko
AU - Hasegawa, Yuki
AU - Hashikawa, Tsutomu
AU - Tomomura, Akito
AU - Yuzaki, Michisuke
AU - Furuichi, Teiichi
AU - Yano, Ryoji
N1 - Funding Information:
We would like to thank Dr. Premkumar Reddy and Dr. Stacey J. Baker of the Fels Institute for Cancer Research and Molecular Biology (Philadelphia, PA, USA) for providing anti-AATYK antibody, and Ms. Naoko Shinya for her technical assistance. This research was supported by grants-in-aid for Scientific Research from the Japanese Ministry of Education, Culture, Sports, Science and Technology and the Japan Society for the Promotion of Science and by the Institute of Physical and Chemical Research (RIKEN).
PY - 2003/4/10
Y1 - 2003/4/10
N2 - 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.
AB - 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.
KW - Cerebellar granule cell
KW - Immunohistochemistry
KW - Neurite outgrowth
KW - Tyrosine kinase
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U2 - 10.1016/S0169-328X(03)00054-8
DO - 10.1016/S0169-328X(03)00054-8
M3 - Article
C2 - 12670708
AN - SCOPUS:0037430921
SN - 0006-8993
VL - 112
SP - 103
EP - 112
JO - Molecular Brain Research
JF - Molecular Brain Research
IS - 1-2
ER -