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Na+ - and Cl-dependent neurotransmitter transporters in bovine retina: Identification and localization by in situ hybridization histochemistry

Published online by Cambridge University Press:  02 June 2009

Eugenia M. C. Jones
Affiliation:
Committee on Neurobiology, The University of Chicago, Chicago

Abstract

The physiological actions of biogenic amine and amino-acid neurotransmitters are terminated by their removal from the synaptic cleft by specific high-affinity transport proteins. The members of the Na+- and Cl-dependent neurotransmitter transporter family expressed in bovine retina and responsible for the uptake of biogenic amine and amino-acid neurotransmitters were identified using a reverse transcriptase-polymerase chain reaction-based approach. cDNA clones encoding bovine homologues of glycine (GLYT-1), γ-aminobutyric acid (GAT-1) creatine (CreaT), and orphan (NTT4) transporters were identified using this strategy. The expression pattern of mRNAs encoding these proteins in the retina was determined by in situ hybridization histochemistry GLYT-1 CreaT NTT4 and GAT-1 mRNAs were expressed in the retina by cells in the inner nuclear inner plex, iform and ganglion cell layers They were not expressed at detectable levels in the photoreceptor cells whose cell bodies are in the outer nuclear layer and are the most abundant cell type in the retina GLYT-1 mRNA was present exclusively in the proximal inner nuclear layer GAT-1 mRNA was localized to both the inner nuclear and ganglion cell layers CreaT mRNA was expressed in all cell types in the retina except photoreceptors and NTT4 mRNA was expressed by a sub subpoulation of cells in the ganglion cell laver. Elucidation of the expression pattern of these neurotransmitter transporter mRNAs in the retina provides a basis for studies of the role of glycine γ-aminobutyric acid and creatine transporters in retinal function.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 1995

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References

REFERENCES

Amara, S.G. & Kuhar, M.J. (1993). Neurotransmitter transporters: Recent progress. Annual Review of Neuroscience 16, 7393.CrossRefGoogle ScholarPubMed
Bercer, S.L. & Kimmel, A.R. (1987). Methods in Enzymology. Vol. 152, New York: Academic Press.Google Scholar
Borden, L.A., Smith, K.E., Hartig, P.R., Branchek, T.A. & Wein-shank, R.L. (1992). Molecular heterogeneity of the gamma-amino-butyric acid (GABA) transport system. Cloning of two novel high affinity GABA transporters from rat brain. Journal of Biological Chemistry 26, 2109821104.Google Scholar
Borowsky, B., Mezey, E. & Hoffman, B.J. (1993). Two glycine transporter variants with distinct localization in the CNS and peripheral tissues are encoded by a common gene. Neuron 10, 851863.CrossRefGoogle ScholarPubMed
Brecha, N.C., Sternini, C. & Humphray, M.F. (1991). Cellular distribution of L-glutamate decarboxylase (GAD) and gamma-aminobutyric acid A (GABA-A) receptor mRNAs in the retina. Cellular and Molecular Neurobiology 11, 497509.CrossRefGoogle ScholarPubMed
Cohen, E. & Sterling, P. (1986). Accumulation of (3H)glycine by cone bipolar neurons in the cat retina. Journal of Comparative Neurology 250, 17.Google Scholar
El Mestikawy, S., Giros, B., Pohl, M., Hamon, M., Kingsmore, S.F., Seldin, M.F. & Caron, M.G. (1994). Characterization of an atypical member of the Na+/Cl dependent transporter family: Chromosomal localization and distribution in GABAergic and glutamatergic neurons in the rat brain. Journal of Neurochemistry 62, 445455.CrossRefGoogle ScholarPubMed
Ehringer, B. & Falck, B. (1971). Autoradiography of some suspected neurotransmitter substances: GABA, glycine, glutamic acid, histamine, dopamine, and L-DOPA. Brain Research 33, 157172.CrossRefGoogle Scholar
Greferath, U., Gruenert, U., Müller, F. & Wässel, H. (1994). Localization of GABA A receptors in the rabbit retina. Cell and Tissue Research 276, 295307.Google Scholar
Gruenert, U. & Wässel, H. (1990). GABA-like immunoreactivity in the macaque monkey retina: A light and electron microscopic study. Journal of Comparative Neurology 297, 509524.CrossRefGoogle Scholar
Guimbal, C. & Kilimann, M.W. (1993). A Na(+)-dependent creatine transporter in rabbit brain, muscle, heart, and kidney. cDNA cloning and functional expression. Journal of Biological Chemistry 26, 84188421.CrossRefGoogle Scholar
Johnson, J.W. & Ascher, P. (1987). Glycine potentiates the NMDA response in cultured mouse brain neurones. Nature 325, 529531.CrossRefGoogle Scholar
Liu, Q.R., Mandiyan, S., Lopez-Corcuera, B., Nelson, H. & Nelson, N. (1993a). A rat brain cDNA encoding the neurotransmitter transporter with an unusual structure. FEBS Letters 315, 114118.CrossRefGoogle ScholarPubMed
Liu, Q.R., Lopez-Corcuera, B., Mandiyan, S., Nelson, H. & Nelson, N. (1993b). Cloning and expression of a spinal cord- and brain-specific glycine transporter with novel structural features. Journal of Biological Chemistry 268, 2280222806.CrossRefGoogle ScholarPubMed
Liu, Q.R., Lopez-Corcuera, B., Mandiyan, S., Nelson, H. & Nelson, N. (1993c). Molecular characterization of four pharmacologically distinct α-aminobutyric acid transporters in mouse brain. Journal of Biological Chemistry 268, 21062121.Google Scholar
Marc, R.E. (1985). The role of glycine in retinal circuitry. In Retinal Transmitters and Modulators: Models for the Brain. Vol. 1, ed. Morgan, W.W., pp. 119158. Boca Raton, Florida: CRC Press.Google Scholar
Nelson, H., Mandiyan, S. & Nelson, N. (1990). Cloning of the human brain GABA transporter. FEBS Letters 269, 181184.Google Scholar
Osborne, N.N. (1980). In vitro experiments on the metabolism, uptake, and release of 5–hydroxytryptamine in bovine retina. Brain Research 184, 283297.Google Scholar
Osborne, N.N. (1981). Noradrenaline, a transmitter candidate in the retina. Journal of Neurochemistry 36, 1727.CrossRefGoogle ScholarPubMed
Pasante-Morales, H. (1985). Taurine function in excitable tissue: The retina as a model. In Retinal Transmitters and Modulators: Models for the Brain. Vol. 2, ed. Morgan, W.W., pp. 3362. Boca Raton, Florida: CRC Press.Google Scholar
Richardson, K.C., Jarett, L. & Finke, E.H. (1960). Embedding in epoxy resin for ultrathin sectioning in electron microscopy. Stain Technology 35, 313323.Google Scholar
Ruiz, M., Egal, H., Sarthy, V., Qian, X. & Sarkar, H.K. (1994). Cloning, expression, and localization of a mouse retinal gamma-aminobutyric acid transporter. Investigative Ophthamology and Visual Science 35, 40394048.Google ScholarPubMed
Sambrook, J., Fritsch, E.F. & Maniatas, T. (1989). Molecular Cloning: A Laboratory Manual. Cold Spring Harbor, Michigan: Cold Spring Harbor Press.Google Scholar
Sarthy, P.V. (1982). The uptake of [3H]gamma-aminobutyric acid by isolated glial (Müller) cells from the mouse retina. Journal of Neuroscience Methods 5, 7782.Google Scholar
Sassoe-Pognetto, M., Wässel, H. & Gruenert, U. (1994). Glycinergic synapses in the rod pathway of the rat retina: Cone bipolar cells express α 1 subunit of the glycine receptor. Journal of Neuroscience 14, 51315146.Google Scholar
Schloss, P., Püschel, A.W. & Betz, H. (1994). Neurotransmitter transporters: New members of known families. Current Opinions in Cell Biology 6, 595599.Google Scholar
Shafat, S., Velaz-Faircloth, M., Guadano-Ferraz, a. & Fremeau, R.T. (1993). Molecular characterization of neurotransmitter transporters. Molecular Endocrinology 7, 15171529.Google Scholar
Simmons, D.M., Arriza, J.L. & Swanson, L.W. (1989). a complete protocol for In situ hybridization of messenger RNAs in brain and other tissues with radio-labeled single-stranded RNA probes. Journal of Histotechnology 12, 169181.Google Scholar
Starr, M.S. (1978). Uptake of taurine by retina in different species. Brain Research 151, 604608.CrossRefGoogle ScholarPubMed
Uhl, G.R. (1992). Neurotransmitter transporters (plus): a promising new gene family. Trends in Neuroscience 15, 265268.CrossRefGoogle Scholar
Wallimann, T. & Eppenberger, H.M. (1990). The subcellular com-partmentation of creatine kinase isozymes as a precondition for a proposed phosphoryl-creatine circuit. Progress in Clinical Biological Research 344, 877889.Google Scholar
Wässel, H. & Chun, M.H. (1989). GaBa-like immunoreactivity in the cat retina: Light microscopy. Journal of Comparative Neurology 279, 4354.Google Scholar