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多系统萎缩症 iPSC 衍生多巴胺能神经元中线粒体失调和自噬受损。

Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System Atrophy.

机构信息

IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan 20122, Italy.

Department of Neurology, Columbia University, New York, NY 10032, USA.

出版信息

Stem Cell Reports. 2018 Nov 13;11(5):1185-1198. doi: 10.1016/j.stemcr.2018.09.007. Epub 2018 Oct 18.

Abstract

Multiple system atrophy (MSA) is a progressive neurodegenerative disease that affects several areas of the CNS, whose pathogenesis is still widely unclear and for which an effective treatment is lacking. We have generated induced pluripotent stem cell-derived dopaminergic neurons from four MSA patients and four healthy controls and from two monozygotic twins discordant for the disease. In this model, we have demonstrated an aberrant autophagic flow and a mitochondrial dysregulation involving respiratory chain activity, mitochondrial content, and CoQ10 biosynthesis. These defective mechanisms may contribute to the onset of the disease, representing potential therapeutic targets.

摘要

多系统萎缩症(MSA)是一种进行性神经退行性疾病,影响中枢神经系统的多个区域,其发病机制仍不清楚,也缺乏有效的治疗方法。我们已经从四名 MSA 患者和四名健康对照者以及两名患有该疾病的异卵双胞胎中生成了诱导多能干细胞衍生的多巴胺能神经元。在该模型中,我们已经证明了异常的自噬流和线粒体失调,涉及呼吸链活性、线粒体含量和 CoQ10 生物合成。这些有缺陷的机制可能有助于疾病的发生,代表了潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/870d/6234905/73992aea7020/gr1.jpg

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