| Literature DB >> 30901725 |
Hannah Meiklejohn1, Md Shaki Mostaid2, Sandra Luza3, Serafino G Mancuso4, Dali Kang4, Sonny Atherton3, Debora A Rothmond5, Cynthia Shannon Weickert6, Carlos M Opazo3, Christos Pantelis7, Ashley I Bush8, Ian P Everall9, Chad A Bousman10.
Abstract
A number of recent studies have suggested the ubiquitin proteasome system (UPS) in schizophrenia is dysfunctional. The purpose of this study was to investigate UBE2K, a ubiquitin-conjugating (E2) enzyme within the UPS that has been associated with psychosis symptom severity, in the blood and brain of individuals with schizophrenia. Whole blood and erythrocytes from 128 (71 treatment-resistant schizophrenia, 57 healthy controls) individuals as well as frozen dorsolateral prefrontal cortex (DLPFC) and orbitofrontal cortex (OFC) post-mortem samples from 74 (37 schizophrenia, 37 controls) individuals were obtained. UBE2K gene expression was assayed in whole blood and DLPFC samples, whereas protein levels were assayed in erythrocytes and OFC samples. Elevated levels of UBE2K mRNA were observed in whole blood of individuals with schizophrenia (p = 0.03) but not in the DLPFC, while protein levels were raised in erythrocytes and the OFC (p < 0.001 and p = 0.002 respectively). Findings were not better explained by age, smoking, clozapine plasma levels or duration of illness. Although blood and brain samples were derived from independent samples, our findings suggest peripheral protein levels of UBE2K may serve as a surrogate of brain levels and further supports the notion of UPS dysfunction in schizophrenia. Future studies to determine the pathophysiological effects of elevated UBE2K protein levels in the brain of those with schizophrenia are warranted.Entities:
Keywords: Gene expression; Post-mortem; Protein expression; Schizophrenia; Treatment-resistant; UBE2K; Ubiquitin
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Year: 2019 PMID: 30901725 DOI: 10.1016/j.jpsychires.2019.03.005
Source DB: PubMed Journal: J Psychiatr Res ISSN: 0022-3956 Impact factor: 4.791