GAT-1, A HIGH-AFFINITY GABA PLASMA-MEMBRANE TRANSPORTER, IS LOCALIZED TO NEURONS AND ASTROGLIA IN THE CEREBRAL-CORTEX

被引:270
作者
MINELLI, A
BRECHA, NC
KARSCHIN, C
DEBIASI, S
CONTI, F
机构
[1] UNIV ANCONA,IST FISIOL UMANA,I-60131 ANCONA,ITALY
[2] UNIV CALIF LOS ANGELES,SCH MED,DEPT NEUROBIOL,LOS ANGELES,CA 90024
[3] UNIV CALIF LOS ANGELES,SCH MED,DEPT MED,LOS ANGELES,CA 90024
[4] UNIV CALIF LOS ANGELES,SCH MED,BRAIN RES INST,LOS ANGELES,CA 90024
[5] UNIV CALIF LOS ANGELES,SCH MED,CURE VA UCLA GASTROENTER BIOL CTR,LOS ANGELES,CA 90024
[6] VET ADM MED CTR,LOS ANGELES,CA 91343
[7] MAX PLANCK INST EXPTL MED,W-3400 GOTTINGEN,GERMANY
[8] UNIV MILAN,DEPT GEN PHYSIOL & BIOCHEM,HISTOL & HUMAN ANAT SECT,MILAN,ITALY
关键词
GABA; GABA TRANSPORTERS; NEOCORTEX; SYNAPSES; NEURONS; ASTROCYTES;
D O I
10.1523/jneurosci.15-11-07734.1995
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
High affinity, GABA plasma membrane transporters influence the action of GABA, the main inhibitory neurotransmitter. The cellular expression of GAT-1, a prominent GABA transporter, has been investigated in the cerebral cortex of adult rats using in situ hybridizaton with S-35-labeled RNA probes and immunocytochemistry with affinity purified polyclonal antibodies directed to the C-terminus of rat GAT-1. GAT-1 mRNA was observed in numerous neurons and in some glial cells. Double-labeling experiments were performed to compare the pattern of GAT-1 mRNA containing and GAD67 immunoreactive cells. The majority of neurons expressing GAT-1 mRNA also contained GAD67 immunoreactivity (ir), but GAT-1 mRNA was also observed in a few pyramidal neurons. GAT-1-ir was localized to numerous puncta and fibers and to astrocytic processes, was not observed in sections incubated in GAT-1 antibodies preadsorbed with rat GAT-1 C-terminal peptide, and was observed in sections incubated in GAT-1 antibodies preadsorbed with the C-terminal portion of the related peptides rat GAT3(607-627) or rat glycine transporter-1(625-633). The highest number of GAT-1-ir puncta was in layer IV, followed by layers II-III. GAT-1 positive puncta appeared to have a preferential relationship to the soma and proximal dendrites of unlabeled pyramidal cells. All GAT-1 positive axon terminals formed symmetric synapses. This study demonstrates that (1) GAT-1 is expressed by both neurons and astrocytes, (2) the majority of GAT-1 expressing neurons contain GAD67, and (3) GAT-1 uptake system is more extensive than the GABA synthetizing system. These observations support the hypothesis that, in addition to its role in terminating GABA action by uptake into GABAergic axon terminals, GAT-1 influences both excitatory and inhibitory transmission by modulating the ''paracrine'' spread of GABA (Isaacson et al., 1993), and suggest that astrocytes may play an important role in this process.
引用
收藏
页码:7734 / 7746
页数:13
相关论文
共 99 条
[1]   NONVESICULAR RELEASE OF NEUROTRANSMITTER [J].
ATTWELL, D ;
BARBOUR, B ;
SZATKOWSKI, M .
NEURON, 1993, 11 (03) :401-407
[2]   COMPETITIVE INHIBITION OF GABA UPTAKE IN RAT-BRAIN SLICES BY SOME GABA ANALOGS OF RESTRICTED CONFORMATION [J].
BEART, PM ;
JOHNSTON, GA ;
UHR, ML .
JOURNAL OF NEUROCHEMISTRY, 1972, 19 (08) :1855-&
[3]   NUMERICAL DATA ON NEOCORTICAL NEURONS IN ADULT-RAT, WITH SPECIAL REFERENCE TO THE GABA POPULATION [J].
BEAULIEU, C .
BRAIN RESEARCH, 1993, 609 (1-2) :284-292
[4]  
BIGNAMI A, 1973, J COMP NEUROL, V153, P27
[5]  
BLOOM FE, 1970, NATURE, V229, P628
[6]  
BONANNO G, 1992, TRENDS NEUROSCI, V15, P482, DOI 10.1016/0166-2236(92)90093-N
[7]  
Borden L. A., 1994, Society for Neuroscience Abstracts, V20, P919
[8]  
BORDEN LA, 1992, J BIOL CHEM, V267, P21098
[9]   TIAGABINE, SK-AND-F 89976-A, CI-966, AND NNC-711 ARE SELECTIVE FOR THE CLONED GABA TRANSPORTER GAT-1 [J].
BORDEN, LA ;
DHAR, TGM ;
SMITH, KE ;
WEINSHANK, RL ;
BRANCHEK, TA ;
GLUCHOWSKI, C .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1994, 269 (02) :219-224
[10]   SELECTIVE-INHIBITION OF NEURONAL GABA UPTAKE BY CIS-1,3-AMINOCYCLOHEXANE CARBOXYLIC-ACID [J].
BOWERY, NG ;
JONES, GP ;
NEAL, MJ .
NATURE, 1976, 264 (5583) :281-284