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TC10β/CDC42 GTPASE ACTIVATING PROTEIN IS REQUIRED FOR THE GROWTH OF CORTICAL NEURON DENDRITES
被引:6
|作者:
Shen, P. -C.
[1
]
Xu, D. -F.
[1
]
Liu, J. -W.
[1
]
Li, K.
[1
]
Lin, M.
[1
]
Wang, H. -T.
[1
]
Wang, R.
[1
]
Zheng, J.
[1
]
机构:
[1] E China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
TCGAP;
cortical neurons;
dendritic growth;
dendrite elaboration;
spine formation;
axonal morphogenesis;
FYN TYROSINE KINASE;
MENTAL-RETARDATION;
SPINE MORPHOLOGY;
RHO-GTPASES;
BRAIN;
MORPHOGENESIS;
P250GAP;
RECEPTOR;
CORTEX;
ANOMALIES;
D O I:
10.1016/j.neuroscience.2011.08.053
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Neuronal morphogenesis plays an important role in neuronal development. TC10 beta/CDC42 GTPase-activating protein (TCGAP) is known to be a brain-enriched multiple domain protein, but its role in neuronal development process remains poorly understood. In the present study, we showed that TCGAP positively regulated dendritic outgrowth and spine formation in developing cortical neurons. Knocking down TCGAP by RNA interference led to a decrease in the overall length of dendrite arbors and the number of dendrite branches both in vitro and in vivo. Overexpressing TCGAP in cultured cortical neurons increased dendritic outgrowth and branching. Moreover, overexpressing TCGAP lead to an increase of spine density while knocking-down TCGAP decreased spine density in vivo. The defect by downregulating TCGAP could be rescued by expressing a knock-down resistant form of TCGAP both in vivo and in vitro. In contrast, neither downregulating nor overexpressing TCGAP had any effect on axonal morphogenesis in primary cortical neuron cultures. Together, our findings suggest that TCGAP regulates neuronal morphogenesis in developing cortical neurons at both early and late stage. (C) 2011 Published by Elsevier Ltd on behalf of IBRO.
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页码:589 / 597
页数:9
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