Literature DB >> 22332935

Lateral regions of the rodent striatum reveal elevated glutamate decarboxylase 1 mRNA expression in medium-sized projection neurons.

Stefan Trifonov1, Takeshi Houtani, Masahiko Kase, Kazunori Toida, Masato Maruyama, Yuji Yamashita, Jun-Ichi Shimizu, Tetsuo Sugimoto.   

Abstract

The GABA-synthesizing enzymes glutamate decarboxylase (GAD)1 and GAD2 are universally contained in GABAergic neurons in the central nervous system of the mouse and rat. The two isoforms are almost identically expressed throughout the brain and spinal cord. By using in situ hybridization, we found that the mouse lateral striatum concentrates medium-sized projection neurons with high-level expression of GAD1, but not of GAD2, mRNA. This was confirmed with several types of riboprobe, including those directed to the 5'-noncoding, 3'-noncoding and coding regions. Immunohistochemical localization of GAD1 also revealed predominant localization of the enzyme in the same striatal region. The lateral region of the mouse striatum, harboring such neurons, is ovoid in shape and extends between interaural +4.8 and +2.8, and at lateral 2.8 and dorsoventral 2.0. This intriguing region corresponds to the area that receives afferent inputs from the primary motor and sensory cortex that are presumably related to mouth and forelimb representations. The lateral striatum is included in the basal ganglia-thalamocortical loop, and is most vulnerable to various noxious stimuli in the neurodegeneration processes involving the basal ganglia. We have confirmed elevated expression of GAD1 mRNA, but not of GAD2 mRNA, also in the rat lateral striatum. Image analysis favored the view that the regional increase is caused by elevated cellular expression, and that the greatest number of medium-sized spiny neurons were positive for GAD1 mRNA. The GAD1 mRNA distribution in the mouse lateral striatum partially resembled those of GPR155 and cannabinoid receptor type 1 mRNAs, suggesting functional cooperation in some neurons.
© 2012 The Authors. European Journal of Neuroscience © 2012 Federation of European Neuroscience Societies and Blackwell Publishing Ltd.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22332935     DOI: 10.1111/j.1460-9568.2012.08001.x

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


  5 in total

1.  Deep sequencing of the murine olfactory receptor neuron transcriptome.

Authors:  Ninthujah Kanageswaran; Marilen Demond; Maximilian Nagel; Benjamin S P Schreiner; Sabrina Baumgart; Paul Scholz; Janine Altmüller; Christian Becker; Julia F Doerner; Heike Conrad; Sonja Oberland; Christian H Wetzel; Eva M Neuhaus; Hanns Hatt; Günter Gisselmann
Journal:  PLoS One       Date:  2015-01-15       Impact factor: 3.240

2.  Glutamic acid decarboxylase 1 alternative splicing isoforms: characterization, expression and quantification in the mouse brain.

Authors:  Stefan Trifonov; Yuji Yamashita; Masahiko Kase; Masato Maruyama; Tetsuo Sugimoto
Journal:  BMC Neurosci       Date:  2014-10-16       Impact factor: 3.288

3.  Evolution of the Membrane Transport Protein Domain.

Authors:  Siarhei A Dabravolski; Stanislav V Isayenkov
Journal:  Int J Mol Sci       Date:  2022-07-22       Impact factor: 6.208

4.  Characterization of GABAergic neurons in the mouse lateral septum: a double fluorescence in situ hybridization and immunohistochemical study using tyramide signal amplification.

Authors:  Changjiu Zhao; Brian Eisinger; Stephen C Gammie
Journal:  PLoS One       Date:  2013-08-13       Impact factor: 3.240

5.  Estradiol Facilitates Functional Integration of iPSC-Derived Dopaminergic Neurons into Striatal Neuronal Circuits via Activation of Integrin α5β1.

Authors:  Kaneyasu Nishimura; Daisuke Doi; Bumpei Samata; Shigeo Murayama; Tsuyoshi Tahara; Hirotaka Onoe; Jun Takahashi
Journal:  Stem Cell Reports       Date:  2016-03-17       Impact factor: 7.765

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.