TRPC3aEurodependent synaptic transmission in central mammalian neurons

被引:19
作者
Hartmann, Jana [1 ,2 ,3 ]
Konnerth, Arthur [1 ,2 ,3 ]
机构
[1] Tech Univ Munich, Inst Neurosci, D-80802 Munich, Germany
[2] Munich Cluster Syst Neurol SyNergy, Munich, Germany
[3] Ctr Integrated Prot Sci CIPSM, Munich, Germany
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2015年 / 93卷 / 09期
基金
欧洲研究理事会;
关键词
Cerebellum; Purkinje cell; mGluR1; STIM1; Ataxia; METABOTROPIC GLUTAMATE RECEPTORS; TRPC3; CHANNELS; PHOSPHOLIPASE-C; CEREBELLAR; CALCIUM; RELEASE; ACTIVATION; EXPRESSION; CURRENTS; DOMAIN;
D O I
10.1007/s00109-015-1298-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The transient receptor potential (TRPC) proteins form non-selective cation channels that are activated downstream of G(q)-phospholipase C-coupled receptors. TRPC3, one of the seven members of the TRPC subfamily, combines functions of an unspecific ion channel and a signal transducer. In the mammalian brain, the expression of TRPC3 is highest in cerebellar Purkinje cells, the principal neurons, and the sole output of the cerebellar cortex. In this review, we summarize findings identifying TRPC3 channels as integral components of glutamatergic metabotropic synaptic transmission. We give an overview of postsynaptic interaction partners and activation mechanisms of TRPC3 in central neurons. Finally, we address the deleterious consequences of distorted TRPC3 synaptic signaling for cerebellar function in different mouse models and present TRPC3 as an emerging candidate protein implicated in various forms of ataxia in humans.
引用
收藏
页码:983 / 989
页数:7
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