The TRPM7 ion channel functions in cholinergic synaptic vesicles and affects transmitter release

被引:168
作者
Krapivinsky, Grigory
Mochida, Sumiko
Krapivinsky, Luba
Cibulsky, Susan M.
Clapham, David E.
机构
[1] Childrens Hosp, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
[3] Tokyo Med Univ, Dept Physiol, Tokyo 1608402, Japan
关键词
D O I
10.1016/j.neuron.2006.09.033
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A longstanding hypothesis is that ion channels are present in the membranes of synaptic vesicles and might affect neurotransmitter release. Here we demonstrate that TRPM7, a member of the transient receptor potential (TRP) ion channel family, resides in the membrane of synaptic vesicles of sympathetic neurons, forms molecular complexes with the synaptic vesicle proteins synapsin I and synaptotagmin 1, and directly interacts with synaptic vesicular snapin. In sympathetic neurons, changes in TRPM7 levels and channel activity alter acetylcholine release, as measured by EPSP amplitudes and decay times in postsynaptic neurons. TRPM7 affects EPSP quantal size, an intrinsic property of synaptic vesicle release. Targeted peptide interference of TRPM7's interaction with snapin affects the amplitudes and kinetics of postsynaptic EPSPs. Thus, vesicular TRPM7 channel activity is critical to neurotransmitter release in sympathetic neurons.
引用
收藏
页码:485 / 496
页数:12
相关论文
共 51 条
[1]  
Bennett M R, 1972, Monogr Physiol Soc, P1
[2]   Rapid vesicular translocation and insertion of TRP channels [J].
Bezzerides, VJ ;
Ramsey, IS ;
Kotecha, S ;
Greka, A ;
Clapham, DE .
NATURE CELL BIOLOGY, 2004, 6 (08) :709-720
[3]   MORPHOLOGICAL-STUDIES OF SYNAPSES AND VARICOSITIES IN DISSOCIATED CELL-CULTURES OF SYMPATHETIC NEURONS [J].
BUCKLEY, KM ;
LANDIS, SC .
JOURNAL OF NEUROCYTOLOGY, 1983, 12 (01) :67-92
[4]   Splitting the quantum: regulation of quantal release during vesicle fusion [J].
Burgoyne, RD ;
Barclay, JW .
TRENDS IN NEUROSCIENCES, 2002, 25 (04) :176-178
[5]   Identification and characterization of Snapin as a ubiquitously expressed SNARE-binding protein that interacts with SNAP23 in non-neuronal cells [J].
Buxton, P ;
Zhang, XM ;
Walsh, B ;
Sriratana, A ;
Schenberg, I ;
Manickam, E ;
Rowe, T .
BIOCHEMICAL JOURNAL, 2003, 375 :433-440
[6]   ISOLATION AND CHARACTERIZATION OF POSTSYNAPTIC DENSITIES FROM VARIOUS BRAIN-REGIONS - ENRICHMENT OF DIFFERENT TYPES OF POSTSYNAPTIC DENSITIES [J].
CARLIN, RK ;
GRAB, DJ ;
COHEN, RS ;
SIEKEVITZ, P .
JOURNAL OF CELL BIOLOGY, 1980, 86 (03) :831-843
[7]   Synaptotagmin:: A Ca2+ sensor that triggers exocytosis? [J].
Chapman, ER .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (07) :498-508
[8]   Phosphorylation of Snapin by PKA modulates its interaction with the SNARE complex [J].
Chheda, MG ;
Ashery, U ;
Thakur, P ;
Rettig, J ;
Sheng, ZH .
NATURE CELL BIOLOGY, 2001, 3 (04) :331-338
[9]   Synapsin dispersion and reclustering during synaptic activity [J].
Chi, P ;
Greengard, P ;
Ryan, TA .
NATURE NEUROSCIENCE, 2001, 4 (12) :1187-1193
[10]   TRP channels as cellular sensors [J].
Clapham, DE .
NATURE, 2003, 426 (6966) :517-524