Literature DB >> 9753172

A rat G protein-coupled receptor selectively expressed in myelin-forming cells.

J Allard1, S Barrón, J Diaz, C Lubetzki, B Zalc, J C Schwartz, P Sokoloff.   

Abstract

By screening an olfactory bulb cDNA library using dopamine receptor probes, we isolated the cDNA coding for the rat counterpart of an orphan receptor known as Edg-2, homologous to G protein-coupled receptors. In situ hybridization analysis showed that Edg-2 mRNA expression is restricted to myelinated structures, e.g. corpus callosum or peripheral nerves. A weaker expression in various peripheral organs was also detected in newborns. A 3.8-kb transcript was found at high levels in highly myelinated brain structures and sciatic nerve, and, at lower levels, in poorly myelinated peripheral organs, consistent with its occurrence in Schwann cells in the peripheral nervous system. One hundred percent of Edg-2 mRNA-containing cells in the brain also expressed mRNA encoding myelin-basic-protein, a marker of oligodendrocytes. This restricted olygodendrocytes localization was confirmed by the absence of cellular colocalization of Edg-2 and glial fibrillary acidic protein, an astrocytic marker. During prenatal development, Edg-2 mRNA expression was high in the cortical neuroepithelium and meningeal layer at E16, extended later to other neuroepithelia, and disappeared shortly after birth. During brain postnatal development, Edg-2 mRNA expression in myelinated structures followed a caudo-rostral gradient, similar to that of myelination. Thus, Edg-2 is the first G protein-coupled receptor found to be selectively expressed in myelin-forming cells in the nervous system and its temporal expression pattern is consistent with a dual role (i) in neurogenesis, during embryonic development, and (ii) in myelination and myelin maintenance, during postnatal life.

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Year:  1998        PMID: 9753172     DOI: 10.1046/j.1460-9568.1998.00117.x

Source DB:  PubMed          Journal:  Eur J Neurosci        ISSN: 0953-816X            Impact factor:   3.386


  17 in total

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2.  Lysophosphatidic acid can support the formation of membranous structures and an increase in MBP mRNA levels in differentiating oligodendrocytes.

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3.  Lysophosphatidic acid (LPA) and its receptor, LPA1 , influence embryonic schwann cell migration, myelination, and cell-to-axon segregation.

Authors:  Brigitte Anliker; Ji Woong Choi; Mu-En Lin; Shannon E Gardell; Richard R Rivera; Grace Kennedy; Jerold Chun
Journal:  Glia       Date:  2013-09-24       Impact factor: 7.452

4.  Exploratory, anxiety and spatial memory impairments are dissociated in mice lacking the LPA1 receptor.

Authors:  Estela Castilla-Ortega; Jorge Sánchez-López; Carolina Hoyo-Becerra; Elisa Matas-Rico; Emma Zambrana-Infantes; Jerold Chun; Fernando Rodríguez De Fonseca; Carmen Pedraza; Guillermo Estivill-Torrús; Luis J Santin
Journal:  Neurobiol Learn Mem       Date:  2010-04-11       Impact factor: 2.877

5.  Neurochemical changes in LPA1 receptor deficient mice--a putative model of schizophrenia.

Authors:  Claire Roberts; Panida Winter; Claire S Shilliam; Zoe A Hughes; Christopher Langmead; Peter R Maycox; Lee A Dawson
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Review 6.  Lysophospholipid receptor nomenclature review: IUPHAR Review 8.

Authors:  Yasuyuki Kihara; Michael Maceyka; Sarah Spiegel; Jerold Chun
Journal:  Br J Pharmacol       Date:  2014-07-12       Impact factor: 8.739

Review 7.  Lysophospholipid receptors in the nervous system.

Authors:  Rachelle E Toman; Sarah Spiegel
Journal:  Neurochem Res       Date:  2002-08       Impact factor: 3.996

Review 8.  Lysophospholipids and their receptors in the central nervous system.

Authors:  Ji Woong Choi; Jerold Chun
Journal:  Biochim Biophys Acta       Date:  2012-07-31

9.  Deletion of lysophosphatidic acid receptor LPA1 reduces neurogenesis in the mouse dentate gyrus.

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Journal:  Mol Cell Neurosci       Date:  2008-07-29       Impact factor: 4.314

10.  Characterization of lpa(2) (Edg4) and lpa(1)/lpa(2) (Edg2/Edg4) lysophosphatidic acid receptor knockout mice: signaling deficits without obvious phenotypic abnormality attributable to lpa(2).

Authors:  James J A Contos; Isao Ishii; Nobuyuki Fukushima; Marcy A Kingsbury; Xiaoqin Ye; Shuji Kawamura; Joan Heller Brown; Jerold Chun
Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

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