Regulation of neuregulin signaling by PSD-95 interacting with ErbB4 at CNS synapses

被引:327
作者
Huang, YZ
Won, S
Ali, DW
Wang, Q
Tanowitz, M
Du, QS
Pelkey, KA
Yang, DJ
Xiong, WC
Salter, MW
Mei, L [1 ]
机构
[1] Univ Alabama Birmingham, Dept Neurobiol Pathol & Phys Med & Rehabil, Birmingham, AL 35294 USA
[2] Univ Virginia, Dept Pharmacol, Charlottesville, VA 22908 USA
[3] Chinese Acad Sci, Inst Neurosci, Mol Neurobiol Lab, Shanghai 200031, Peoples R China
[4] Shanghai Res Ctr Life Sci, Shanghai 200031, Peoples R China
[5] Univ Toronto, Hosp Sick Children, Dept Physiol, Program Brain & Behav, Toronto, ON M5G 1X8, Canada
[6] Univ Toronto, Hosp Sick Children, Dept Physiol, Cell Biol Program, Toronto, ON M5G 1X8, Canada
[7] Georgetown Univ, Vincent T Lombardi Canc Res Ctr, Washington, DC 20007 USA
[8] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
D O I
10.1016/S0896-6273(00)81176-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuregulins (NRGs) and their receptors, the ErbB protein tyrosine kinases, are essential for neuronal development, but their functions in the adult CNS are unknown. We report that ErbB4 is enriched in the postsynaptic density (PSD) and associates with PSD-95. Heterologous expression of PSD-95 enhanced NRG activation of ErbB4 and MAP kinase. Conversely, inhibiting expression of PSD-95 in neurons attenuated NRG-mediated activation of MAP kinase. PSD-95 formed a ternary complex with two molecules of ErbB4, suggesting that PSD-95 facilitates ErbB4 dimerization. Finally, NRG suppressed induction of long-term potentiation in the hippocampal CA1 region without affecting basal synaptic transmission. Thus, NRG signaling may be synaptic and regulated by PSD-95. A role of NRG signaling in the adult CNS may be modulation of synaptic plasticity.
引用
收藏
页码:443 / 455
页数:13
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