Transcribing β-cell mitochondria in health and disease.

Transcribing β-cell mitochondria in health and disease.
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DOI:
10.1016/j.molmet.2017.05.014
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发表时间:
2017-09
影响因子:
8.1
通讯作者:
Mulder H
Mulder H
中科院分区:
医学1区
文献类型:
--
作者:
Mulder H

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最近的2型糖尿病(T2D)全基因组关联研究(GWAS)已经确定胰腺β细胞是该疾病发病机制的罪魁祸首。线粒体代谢在控制胰岛素释放和β细胞质量的过程中发挥着至关重要的作用。这一概念意味着控制线粒体功能的机制有可能在T2D中发挥决定性的致病作用。本文综述的研究表明,确实有线粒体功能障碍的胰岛在T2D,和GWAS已经确定了一个变种的基因编码转录因子B1线粒体(TFB1M),诱发T2D由于线粒体功能障碍和胰岛素分泌受损。这种致病联系的性质,以及其他线粒体转录因子的机制研究,描述。基于此,认为线粒体中的转录和翻译是决定健康和疾病中β细胞中线粒体功能的关键过程。
The recent genome-wide association studies (GWAS) of Type 2 Diabetes (T2D) have identified the pancreatic β-cell as the culprit in the pathogenesis of the disease. Mitochondrial metabolism plays a crucial role in the processes controlling release of insulin and β-cell mass. This notion implies that mechanisms controlling mitochondrial function have the potential to play a decisive pathogenetic role in T2D. This article reviews studies demonstrating that there is indeed mitochondrial dysfunction in islets in T2D, and that GWAS have identified a variant in the gene encoding transcription factor B1 mitochondrial (TFB1M), predisposing to T2D due to mitochondrial dysfunction and impaired insulin secretion. Mechanistic studies of the nature of this pathogenetic link, as well as of other mitochondrial transcription factors, are described. Based on this, it is argued that transcription and translation in mitochondria are critical processes determining mitochondrial function in β-cells in health and disease.
DOI: 10.1038/nature18642
发表时间: 2016-08-04
期刊: NATURE
影响因子: 64.8
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发表时间: 2015
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