Calcineurin acts via the C-terminus of NR2A to modulate desensitization of NMDA receptors

被引:98
作者
Krupp, JJ
Vissel, B
Thomas, CG
Heinemann, SF
Westbrook, GL
机构
[1] Oregon Hlth & Sci Univ, Vollum Inst, Portland, OR 97201 USA
[2] Salk Inst Biol Studies, La Jolla, CA 92037 USA
关键词
calcineurin; NMDA receptors; desensitization; tyrosine phosphatases; mutagenesis; patch-clamp;
D O I
10.1016/S0028-3908(02)00031-X
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Phosphatase IIb (calcineurin, CaN) can reduce N-methyl-D-aspartate (NMDA) synaptic responses by enhancing glycine-independent desensitization. We examined the action of CaN on desensitization in recombinant NMDA receptors comprised of NMDA receptor 1 (NR1) and NR2A subunits. The C-terminus of NR2A, but not NR1, was critical for modulation of desensitization by CaN. Alanine-scanning mutagenesis indicated that serines 900 and 929 in NR2A altered desensitization, as did inhibition of tyrosine phosphatases. Our data suggest that dephosphorylation-dependent regulation of the C-terminus of NR2A increases desensitization of NMDA receptors, providing an additional mechanism for modulation of synaptic signals. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:593 / 602
页数:10
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