Glycinergic miniature synaptic currents and receptor cluster sizes differ between spinal cord interneurons

被引:33
作者
Oleskevich, S
Alvarez, FJ
Walmsley, B
机构
[1] Australian Natl Univ, Div Neurosci, John Curtin Sch Med Res, Synapt Structure & Funct Grp, Canberra, ACT 2601, Australia
[2] Wright State Univ, Dayton, OH 45435 USA
关键词
D O I
10.1152/jn.1999.82.1.312
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The structural features of a synaptic connection between central neurons play an important role in determining the strength of the connection. In the present study, we have examined the relationship between the structural and functional properties of glycinergic synapses in the rat spinal cord. We have analyzed the structure of glycinergic receptor clusters on rat ventral horn interneurons using antibodies against the glycine receptor clustering protein, gephyrin. We have examined the properties of quantal glycinergic currents generated at these synapses using whole cell parch-clamp recordings of miniature postsynaptic inhibitory currents (mIPSCs) in rat spinal cord slices in vitro. Our immunolabeling results demonstrate that there is a considerable variability in the size of glycine receptor clusters within individual neurons. Furthermore there are large differences in the mean cluster size between neurons. These observations are paralleled closely by recordings of glycinergic mIPSCs. The mIPSC amplitude varies significantly within and between neurons. Results obtained using combined immunolabeling and electrophysiological recording on the same neurons show that cells with small glycine receptor clusters concurrently exhibit small mIPSCs. Our results suggest that the differences in the size of glycinergic receptor clusters may constitute an important factor contributing to the observed differences in mIPSC amplitude among spinal cord interneurons.
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收藏
页码:312 / 319
页数:8
相关论文
共 38 条
[1]   Distribution of cholinergic contacts on Renshaw cells in the rat spinal cord: a light microscopic study [J].
Alvarez, FJ ;
Dewey, DE ;
McMillin, P ;
Fyffe, REW .
JOURNAL OF PHYSIOLOGY-LONDON, 1999, 515 (03) :787-797
[2]  
Alvarez FJ, 1997, J COMP NEUROL, V379, P150
[3]  
Aprison M. H., 1990, GLYCINE NEUROTRANSMI, P1
[4]   Expression of glycine receptor alpha subunits and gephyrin in cultured spinal neurons [J].
Bechade, C ;
Colin, I ;
Kirsch, J ;
Betz, H ;
Triller, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1996, 8 (02) :429-435
[5]  
BECKER CM, 1988, EMBO J, V7, P1358
[6]   CONTRIBUTIONS OF DENDRITIC SPINES AND PERFORATED SYNAPSES TO SYNAPTIC PLASTICITY [J].
CALVERLEY, RKS ;
JONES, DG .
BRAIN RESEARCH REVIEWS, 1990, 15 (03) :215-249
[7]   Calbindin D28k expression in immunohistochemically identified Renshaw cells [J].
Carr, PA ;
Alvarez, FJ ;
Leman, EA ;
Fyffe, REW .
NEUROREPORT, 1998, 9 (11) :2657-2661
[8]   Detection of spontaneous synaptic events with an optimally scaled template [J].
Clements, JD ;
Bekkers, JM .
BIOPHYSICAL JOURNAL, 1997, 73 (01) :220-229
[9]   Transmitter timecourse in the synaptic cleft: Its role in central synaptic function [J].
Clements, JD .
TRENDS IN NEUROSCIENCES, 1996, 19 (05) :163-171
[10]  
Colin I, 1998, J COMP NEUROL, V398, P359