Reduced expression of G protein-coupled receptor kinases in schizophrenia but not in schizoaffective disorder

被引:33
|
作者
Bychkov, E. R. [1 ]
Ahmed, M. R. [1 ]
Gurevich, V. V. [1 ]
Benovic, J. L. [2 ]
Gurevich, E. V. [1 ]
机构
[1] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[2] Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
关键词
G protein-coupled receptor kinase; Arrestin; Schizophrenia; Schizoaffective disorder; Postmortem; Protein expression; RNAse protection assay; mRNA expression; SEROTONIN 2A RECEPTOR; PREFRONTAL CORTEX; IN-VIVO; BETA-ARRESTIN; MESSENGER-RNA; RAT-BRAIN; HIPPOCAMPAL-NEURONS; NEOSTRIATAL NEURONS; BIPOLAR DISORDER; TRANSGENIC MICE;
D O I
10.1016/j.nbd.2011.07.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alterations of multiple G protein-mediated signaling pathways are detected in schizophrenia. G protein-coupled receptor kinases (GRKs) and arrestins terminate signaling by G protein-coupled receptors exerting a powerful influence on receptor functions. Modifications of arrestin and/or GRKs expression may contribute to schizophrenia pathology. Cortical expression of arrestins and GRKs was measured postmortem in control and subjects with schizophrenia or schizoaffective disorder. Additionally, arrestin/GRK expression was determined in elderly patients with schizophrenia and age-matched control. Patients with schizophrenia, but not schizoaffective disorder, displayed a reduced concentration of arrestin and GRK mRNAs and GRK3 protein. Arrestins and GRK significantly decreased with age. In elderly patients, GRK6 was reduced, with other GRKs and arrestins unchanged. A reduced cortical concentration of GRKs in schizophrenia (resembling that in aging) may result in altered G protein-dependent signaling, thus contributing to prefrontal deficits in schizophrenia. The data suggest distinct molecular mechanisms underlying schizophrenia and schizoaffective disorder. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:248 / 258
页数:11
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