神经元和β细胞中的REST/NRSF靶基因:糖尿病和神经退行性疾病的病理生理和治疗观点

A. Abderrahmani
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引用次数: 1

摘要

胰腺β和神经元细胞有许多相似之处,包括分化程序的关键转录机制。其机制涉及转录抑制因子re -1沉默转录因子(REST)的减少或消失,也称为神经元限制性沉默因子(NRSF),导致编码成熟β和神经元细胞功能所需蛋白质的各种基因的表达。一些REST/NRSF靶基因的异常表达和遗传变异已经在糖尿病和神经退行性疾病中被报道,这表明在这两种疾病中,共同的致病机制解释了β细胞下降和神经元变性。此外,一些REST/NRSF靶基因已被确定为改善糖尿病β细胞功能的潜在治疗靶点。这篇综述揭示了神经元和β细胞REST/NRSF靶基因是未来治疗糖尿病和神经变性的潜在药物靶点。
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REST/NRSF Target Genes in Neuronal and Beta Cells: Pathophysiological and Therapeutic Perspectives for Diabetes and Neurodegenerative Disorders
Pancreatic beta and neuronal cells share numerous similarities, including a key transcriptional mechanism of the differentiation programme. The mechanism involves the decrease or the extinction of the transcriptional repressor RE-1-silencing transcription factor (REST), also called neuron-restrictive silencer factor (NRSF), which leads to the expression of various genes encoding proteins required for mature beta and neuronal cell function. Abnormal expression and genetic variation in some of the REST/NRSF target genes have been reported in diabetes and neurodegenerative disorders, suggesting that common pathogenic mechanisms account for beta-cell decline and neuronal degeneration in the two diseases. In addition, some of the REST/NRSF target genes have been identified as potential therapeutic targets for improvement of beta-cell function in diabetes. This review sheds light on the neuronal and beta-cell REST/NRSF target genes that are potential future drug targets for the treatment of diabetes and neurodegeneration.
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