Literature DB >> 11720708

Distribution of an orphan G-protein coupled receptor (JP05) mRNA in the human brain.

S Brézillon1, M Detheux, M Parmentier, T Hökfelt, Y L Hurd.   

Abstract

JP05, also called GPR72 or GIR, is an orphan G-protein-coupled receptor, GPCR, showing significant structural similarity to the tachykinin receptors. The anatomical distribution of JP05 mRNA was first described in the central nervous system of the mouse, and recently the human JP05 orphan receptor gene has been cloned. In the present study the distribution of JP05 mRNA was examined in the human forebrain using in situ hybridization analysis. The results revealed a wide but discrete distribution of the transcript with strongly JP05 mRNA expressing cells, presumably neurons, present in the cerebral cortex (layer II), hippocampus (pyramidal CA3 neurons and granule cells), amygdala (basal and periamygdaloid cortical nuclei), in the endopiriform nucleus, diagonal band of Broca, thalamus (nucleus reuniens, parafascicular nucleus) and hypothalamus (posterior, dorsal, and around the medial mammillary). Weaker signals were detected in the deeper cortical layers and throughout the striatum. A few positive cells were evident in the raphe but not in the substantia nigra or pontine nuclei. The results indicate significant similarities between human and mouse brain with regard to JP05 mRNA expression. The distribution patterns of JP05 mRNA in the human brain suggest involvement in control of emotions and of neuroendocrine, cognitive and motor functions.

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Year:  2001        PMID: 11720708     DOI: 10.1016/s0006-8993(01)03068-2

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  13 in total

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2.  Expression of the glucocorticoid-induced receptor mRNA in rat brain.

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Review 3.  Neuropeptide PEN and Its Receptor GPR83: Distribution, Signaling, and Regulation.

Authors:  Seshat M Mack; Ivone Gomes; Lakshmi A Devi
Journal:  ACS Chem Neurosci       Date:  2019-02-21       Impact factor: 4.418

4.  GPR83 engages endogenous peptides from two distinct precursors to elicit differential signaling.

Authors:  Seshat M Mack; Ivone Gomes; Amanda K Fakira; Mariana L Duarte; Achla Gupta; Lloyd Fricker; Lakshmi A Devi
Journal:  Mol Pharmacol       Date:  2022-05-23       Impact factor: 4.054

Review 5.  Targeting the Recently Deorphanized Receptor GPR83 for the Treatment of Immunological, Neuroendocrine and Neuropsychiatric Disorders.

Authors:  Lindsay M Lueptow; Lakshmi A Devi; Amanda K Fakira
Journal:  Prog Mol Biol Transl Sci       Date:  2018-08-25       Impact factor: 3.622

6.  Identification of GPR83 as the receptor for the neuroendocrine peptide PEN.

Authors:  Ivone Gomes; Erin N Bobeck; Elyssa B Margolis; Achla Gupta; Salvador Sierra; Amanda K Fakira; Wakako Fujita; Timo D Müller; Anne Müller; Matthias H Tschöp; Gunnar Kleinau; Lloyd D Fricker; Lakshmi A Devi
Journal:  Sci Signal       Date:  2016-04-26       Impact factor: 8.192

7.  Downregulation of GPR83 in the hypothalamic preoptic area reduces core body temperature and elevates circulating levels of adiponectin.

Authors:  Jeffrey S Dubins; Manuel Sanchez-Alavez; Victor Zhukov; Alejandro Sanchez-Gonzalez; Gianluca Moroncini; Santos Carvajal-Gonzalez; John R Hadcock; Tamas Bartfai; Bruno Conti
Journal:  Metabolism       Date:  2012-05-04       Impact factor: 8.694

8.  The orphan receptor Gpr83 regulates systemic energy metabolism via ghrelin-dependent and ghrelin-independent mechanisms.

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Journal:  Nat Commun       Date:  2013       Impact factor: 14.919

9.  Molecules affecting hypothalamic control of core body temperature in response to calorie intake.

Authors:  Tamas Bartfai; Bruno Conti
Journal:  Front Genet       Date:  2012-10-05       Impact factor: 4.599

10.  G-protein coupled receptor 83 (GPR83) signaling determined by constitutive and zinc(II)-induced activity.

Authors:  Anne Müller; Gunnar Kleinau; Carolin L Piechowski; Timo D Müller; Brian Finan; Juliane Pratzka; Annette Grüters; Heiko Krude; Matthias Tschöp; Heike Biebermann
Journal:  PLoS One       Date:  2013-01-15       Impact factor: 3.240

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