LOCALIZATION OF MESSENGER-RNAS ENCODING 3 GABA TRANSPORTERS IN RAT-BRAIN - AN IN-SITU HYBRIDIZATION STUDY

被引:171
作者
DURKIN, MM [1 ]
SMITH, KE [1 ]
BORDEN, LA [1 ]
WEINSHANK, RL [1 ]
BRANCHEK, TA [1 ]
GUSTAFSON, EL [1 ]
机构
[1] SYNAPT PHARMACEUT CORP,PARAMUS,NJ 07652
来源
MOLECULAR BRAIN RESEARCH | 1995年 / 33卷 / 01期
关键词
GABA TRANSPORTER; IN SITU HYBRIDIZATION; MESSENGER-RNA; GLIA; MENINGES; BRAIN;
D O I
10.1016/0169-328X(95)00101-W
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Localization of the messenger RNAs encoding three gamma-aminobutyric acid (GABA) transporters, termed GAT-1, GAT-2, and GAT-3, has been carried out in rat brain using radiolabeled oligonucleotide probes and in situ hybridization histochemistry. Hybridization signals for GAT-1 mRNA were observed over many regions of the rat brain, including the retina, olfactory bulb, neocortex, ventral pallidum, hippocampus, and cerebellum. At the microscopic level, this signal appeared to be restricted to neuronal profiles, and the overall distribution of GAT-1 mRNA closely paralleled that seen in other studies with antibodies to GABA. Areas containing hybridization signals for GAT-S mRNA included the retina, olfactory bulb, subfornical organ, hypothalamus, midline thalamus, and brainstem. In some regions, the hybridization signal for GAT-S seemed to be preferentially distributed over glial cells, although hybridization signals were also observed over neurons, particularly in the retina and olfactory bulb. Notably, hybridization signal for GAT-S mRNA was absent from the neocortex and cerebellar cortex, and was very weak in the hippocampus. In contrast to the parenchymal localization obtained for GAT-I and GAT-3 mRNAs, hybridization signals for GAT-2 mRNA were found only over the leptomeninges (pia and arachnoid). The differential distribution of the three GABA transporters described here suggests that while each plays a role in GABA uptake, they do so via distinct cellular populations.
引用
收藏
页码:7 / 21
页数:15
相关论文
共 57 条
  • [1] Barber, Vaughn, Roberts, The cytoarchitecture of GABAergic neurons in rat spinal cord, Brain Res., 238, pp. 305-328, (1982)
  • [2] Belin, Aguera, Tappaz, Degueurce, Bobillier, Pujol, GABA accumulating neurons in the nucleus raphe dorsalis and periaquaductal gray in the rat: a biochemical and autoradiographic study, Brain Res., 170, pp. 279-297, (1979)
  • [3] Borden, Smith, Hartig, Branchek, Weinshank, Molecular heterogeneity of the γ-aminobutyric acid (GABA) transport system. Cloning of two novel high affinity GABA transporters from rat brain, J. Biol. Chem., 267, pp. 21098-21104, (1992)
  • [4] Borden, Smith, Vaysse, Gustafson, Weinshank, Branchek, Reevaluation of GABA transport in neuronal and glial cell cultures correlation of pharmacology and mRNA localization, Receptors Channels, (1995)
  • [5] Bowery, Jones, Neal, Selective inhibition of neuronal GABA uptake by cis-3-aminocyclohexane car☐ylic acid, Nature, 264, pp. 281-284, (1986)
  • [6] Braestrup, Nielsen, Sonnewald, Knutsen, Andersen, Jansen, Frederiksen, Andersen, Mortensen, Suzdak, (R)-N-[4,4-bis(3-methyl-2-thienyl)but-3-en-1yl]nipecotic acid binds with high affinity to the brain γ-aminobutyric acid uptake carrier, J. Neurochem., 54, pp. 639-647, (1990)
  • [7] Brecha, Weigman, Messersmith, Expression of GABA transporter mRNA in the rat central nervous system, Soc. Neurosci. Abstr., 18, (1992)
  • [8] Brecha, Weigmann, Expression of GAT-1, a high-affinity gamma-aminobutyric acid plasma membrane transporter in the rat retina, J. Comp. Neurol., 345, pp. 602-611, (1994)
  • [9] Caruso, Owczarzak, Goebel, Hazlett, Pourcho, GABA-immunoreactivity in ganglion cells of the rat retina, Brain Res., 476, pp. 129-134, (1989)
  • [10] Chesselet, Robbins, Characterization of striatal neurons expressing high levels of glutamic acid decar☐ylase messenger RNA, Brain Res., 492, pp. 237-244, (1989)