Regional alterations in RGS4 protein in schizophrenia
Abstract
The regulator of G protein signaling (RGS) molecules are a class of proteins that modulate the signaling activity of G-protein coupled receptors. Regulator of G protein signaling 4 (RGS4) is of particular interest in schizophrenia since it is associated with the dopamine (DA) receptor, its expression is altered in affected CNS tissue, and polymorphisms in the RGS4 gene are being examined as risk factors for the disease (Morris et al.2004, Am J Med Genet B Neuropsychiatr Genet 125:50-53; Prasad et al.2005, Mol Psychiatry 10:213-219; Williams et al.2004, Biol Psychiatry 55:192-195). To further test for the involvement of RGS4 expression in schizophrenia, we examined a selection of different cortical and subcortical regions in human brain for alterations in RGS4 mRNA and protein expression. To evaluate the effect of antipsychotic medication on RGS4 expression levels, we compared a subset of treated and untreated cases that were off antipsychotic medication for at least 3 months prior to death. We report a significant decrease in RGS4 mRNA levels in the cingulate gyrus, superior frontal gyrus, and the insular cortex of all schizophrenia cases when compared with controls. A decrease in RGS4 mRNA was also observed in the caudate, but only in the medicated schizophrenia cases. Measurement of protein levels using Western blot demonstrated that RGS4 protein is decreased in the frontal cortex of schizophrenia cases.
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RGS4 levels are greatly reduced in the PFC of patients with schizophrenia, and there is evidence of genetic alterations in RGS4 in some families with schizophrenia or bipolar disorder.
“RGS4 levels are greatly reduced in the PFC of patients with schizophrenia134,135, and there is evidence of genetic alterations in RGS4 in some families with schizophrenia or bipolar disorder136,137.”
From Stress signalling pathways that impair prefrontal cortex structure and function (2009) · cites this paper as [135]
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- Authors
- Erdely, H. A., Tamminga, C. A., Roberts, R. C., & Vogel, M. W.
- Affiliations
- University of Maryland, Baltimore (US)
- The University of Texas Southwestern Medical Center (US)
- Corresponding author
- Erdely, Holly A.
- Venue
- Synapse
- Publisher
- Wiley
- Published
- 2006
- Volume
- 59
- Issue
- 8
- Pages
- 472-479
- ISSN
- 0887-4476 (ISSN-L)
- 1098-2396
- OpenAlex
- W1989629219
- Cited by
- 99
- References
- 0
- Citations by year
- 2025: 3 · 2024: 3 · 2023: 2 · 2022: 1 · 2021: 1 · 2020: 3 · 2019: 2 · 2018: 3 · 2017: 1 · 2016: 3 · 2015: 5 · 2014: 2 · 2013: 3 · 2012: 5
- FWCI
- 10.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Synapse (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r03mh067998-02)
- National Institute of Mental Health (R01MH060744, MH 067998, MH60744, MH 62236-01, R01MH062236)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- RGS4, regulator of G protein signaling, schizophrenia, dopamine receptors, G protein-coupled receptors, cingulate gyrus, superior frontal gyrus, insula, caudate nucleus, frontal cortex, antipsychotic drugs, regional brain differences
- MeSH terms
- Adult, Autoradiography, Brain, Female, Humans, Male, Middle Aged, RNA, Messenger, Schizophrenia, Antipsychotic Agents, Blotting, Western, In Situ Hybridization, RGS Proteins
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