MicroRNA-7/Shank3 axis involved in schizophrenia pathogenesis.

J Clin Neurosci

Prevention and Treatment Center for Psychological Diseases, No. 102 Hospital of the Chinese People's Liberation Army, North Peace Road 55, Changzhou, Jiangsu 213003, People's Republic of China. Electronic address:

Published: August 2015

AI Article Synopsis

  • The study compared microRNA-7 (miR-7) expression levels between schizophrenia patients and healthy controls, finding elevated levels in patients.
  • Researchers used a neuron cell line to manipulate miR-7 levels and observed its impact on the SHANK3 gene, which is important for neuronal function.
  • Results suggested that miR-7 negatively regulates SHANK3, indicating that it may influence the development of schizophrenia through alterations in neuronal morphology and function.

Article Abstract

This study aimed to identify the difference of microRNA-7 (miR-7) expression levels between schizophrenia patients and healthy controls and to investigate the regulatory effects of miR-7 on the SHANK3 gene in schizophrenia. miR-7 levels in plasma were detected by quantitative polymerase chain reactions (qPCR) in 50 schizophrenia patients and 50 healthy controls. The hippocampal neuron cell line, HT22, was transfected with lentiviral vector overexpressing or knocking-down miR-7, and the expression levels of SHANK3 mRNA and Shank3 protein were measured by qPCR and immunofluorescence. A luciferase assay was carried out to analyze the regulatory effects of miR-7 on SHANK3. Circulating miR-7 level was significantly increased in schizophrenia patients (p = 0.022). Overexpression of miR-7 suppressed the expression of SHANK3 while the levels of SHANK3 mRNA and Shank protein were significantly increased by miR-7 knockdown. We conclude that miR-7 binds to 3-prime untranslated regions of SHANK3 mRNA and causes the alteration of neuronal morphology and function, potentially playing a crucial role in the pathophysiological process of schizophrenia.

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Source
http://dx.doi.org/10.1016/j.jocn.2015.01.031DOI Listing

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