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树突状谷氨酸释放可在小脑浦肯野细胞中产生代谢型谷氨酸受体1(mGluR1)的自分泌激活。

Dendritic glutamate release produces autocrine activation of mGluR1 in cerebellar Purkinje cells.

作者信息

Shin Jung Hoon, Kim Yu Shin, Linden David J

机构信息

Department of Neuroscience, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, 916 Hunterian Building, Baltimore, MD 21205, USA.

出版信息

Proc Natl Acad Sci U S A. 2008 Jan 15;105(2):746-50. doi: 10.1073/pnas.0709407105. Epub 2008 Jan 3.

Abstract

In recent years, it has become clear that, in addition to conventional anterograde transmission, signaling in neural circuits can occur in a retrograde manner. This suggests the additional possibility that postsynaptic release of neurotransmitter might be able to act in an autocrine fashion. Here, we show that brief depolarization of a cerebellar Purkinje cell triggers a slow inward current. This depolarization-induced slow current (DISC) is attenuated by antagonists of mGluR1 or TRP channels. DISC is eliminated by a mixture of voltage-sensitive Ca2+ channel blockers and is mimicked by a brief climbing fiber burst. DISC is attenuated by an inhibitor of vesicular glutamate transporters or of vesicular fusion. These data suggest that Ca2+-dependent postsynaptic fusion of glutamate-loaded vesicles evokes a slow inward current produced by activation of postsynaptic mGluR1, thereby constituting a useful form of feedback regulation.

摘要

近年来,已经明确的是,除了传统的顺行性传递外,神经回路中的信号传导还可以逆行方式发生。这提示了另一种可能性,即神经递质的突触后释放可能能够以自分泌方式起作用。在这里,我们表明小脑浦肯野细胞的短暂去极化会触发缓慢的内向电流。这种去极化诱导的缓慢电流(DISC)被mGluR1或TRP通道的拮抗剂所减弱。DISC被电压敏感的Ca2+通道阻滞剂混合物消除,并被短暂的攀缘纤维爆发所模拟。DISC被囊泡谷氨酸转运体或囊泡融合抑制剂所减弱。这些数据表明,依赖Ca2+的装载谷氨酸的囊泡的突触后融合会引发由突触后mGluR1激活产生的缓慢内向电流,从而构成一种有用的反馈调节形式。

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