Funahashi Yu, Yoshino Yuta, Iga Jun-Ichi, Ueno Shu-Ichi
Department of Neuropsychiatry, Molecules and Function, Ehime University Graduate School of Medicine, Shitsukawa, Toon, Japan.
World J Biol Psychiatry. 2023 Apr;24(4):303-313. doi: 10.1080/15622975.2022.2104924. Epub 2022 Jul 29.
Recently, the expression changes of microRNAs (miRNAs) in the serum exosomes (EXO) of schizophrenia (SCZ) have been reported. The aim of this study was to investigate the global expression changes of miRNA derived from the plasma EXO of patients with treatment-resistant schizophrenia (TRS) and the effects of clozapine on miRNA expression.
Global miRNA expression changes in plasma EXO between TRS and controls were studied using microarray analysis. Then, miRNA expressions among TRS, non-TRS, and controls were confirmed with quantitative qPCR experiments. We also studied changes in EXO miRNA expression with in-vitro SH-SY5Y cells.
A microarray for miRNA expression analysis (nine controls vs. nine patients with TRS) revealed 13 up- and 18 downregulated miRNAs that were relevant to neuronal and brain development based on gene ontology analysis. Of those, upregulated miR-675-3p expression was successfully validated in the same cohort by qPCR experiments. Conversely, miR-675-3p expression levels were significantly decreased in the non-TRS cohort (50 controls vs. 50 patients without TRS without clozapine treatment).
We identified global miRNA changes in plasma EXO derived from patients with SCZ that were relevant to neuronal functions, among which, hsa-miR-675-3p expression was upregulated by clozapine treatment.
最近,有报道称精神分裂症(SCZ)患者血清外泌体(EXO)中微小RNA(miRNA)的表达发生了变化。本研究的目的是调查难治性精神分裂症(TRS)患者血浆EXO中miRNA的整体表达变化以及氯氮平对miRNA表达的影响。
采用微阵列分析研究TRS患者与对照组血浆EXO中miRNA的整体表达变化。然后,通过定量qPCR实验确认TRS组、非TRS组和对照组之间的miRNA表达。我们还利用体外SH-SY5Y细胞研究了EXO miRNA表达的变化。
基于基因本体分析,一项用于miRNA表达分析的微阵列(9名对照组与9名TRS患者)显示,有13种上调和18种下调的miRNA与神经元和大脑发育相关。其中,qPCR实验在同一队列中成功验证了上调的miR-675-3p的表达。相反,在非TRS队列(50名对照组与50名未接受氯氮平治疗的非TRS患者)中,miR-675-3p的表达水平显著降低。
我们确定了SCZ患者血浆EXO中与神经元功能相关的miRNA整体变化,其中氯氮平治疗可上调hsa-miR-675-3p的表达。