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电压依赖性阴离子通道1(VDAC1)参与结蛋白病中线粒体功能障碍的凋亡过程。

Voltage-Dependent Anion Channel 1(VDAC1) Participates the Apoptosis of the Mitochondrial Dysfunction in Desminopathy.

作者信息

Li Huanyin, Zheng Lan, Mo Yanqing, Gong Qi, Jiang Aihua, Zhao Jing

机构信息

Department of Internal Neurology, Central Hospital of Minhang District, Shanghai (Minhang Hospital, Fudan University), Minhang District, Shanghai, P.R.China.

出版信息

PLoS One. 2016 Dec 12;11(12):e0167908. doi: 10.1371/journal.pone.0167908. eCollection 2016.

Abstract

Desminopathies caused by the mutation in the gene coding for desmin are genetically protein aggregation myopathies. Mitochondrial dysfunction is one of pathological changes in the desminopathies at the earliest stage. The molecular mechanisms of mitochondria dysfunction in desminopathies remain exclusive. VDAC1 regulates mitochondrial uptake across the outer membrane and mitochondrial outer membrane permeabilization (MOMP). Relationships between desminopathies and Voltage-dependent anion channel 1 (VDAC1) remain unclear. Here we successfully constructed the desminopathy rat model, evaluated with conventional stains, containing hematoxylin and eosin (HE), Gomori Trichrome (MGT), (PAS), red oil (ORO), NADH-TR, SDH staining and immunohistochemistry. Immunofluorescence results showed that VDAC1 was accumulated in the desmin highly stained area of muscle fibers of desminopathy patients or desminopathy rat model compared to the normal ones. Meanwhile apoptosis related proteins bax and ATF2 were involved in desminopathy patients and desminopathy rat model, but not bcl-2, bcl-xl or HK2.VDAC1 and desmin are closely relevant in the tissue splices of deminopathies patients and rats with desminopathy at protein lever. Moreover, apoptotic proteins are also involved in the desminopathies, like bax, ATF2, but not bcl-2, bcl-xl or HK2. This pathological analysis presents the correlation between VDAC1 and desmin, and apoptosis related proteins are correlated in the desminopathy. Furthermore, we provide a rat model of desminopathy for the investigation of desmin related myopathy.

摘要

由编码结蛋白的基因突变引起的结蛋白病属于遗传性蛋白质聚集性肌病。线粒体功能障碍是结蛋白病最早出现的病理变化之一。结蛋白病中线粒体功能障碍的分子机制仍不明确。电压依赖性阴离子通道1(VDAC1)调节线粒体外膜的物质摄取以及线粒体膜通透性转换(MOMP)。结蛋白病与VDAC1之间的关系尚不清楚。在此,我们成功构建了结蛋白病大鼠模型,并用苏木精和伊红(HE)、改良Gomori三色染色法(MGT)、过碘酸雪夫染色(PAS)、油红O染色(ORO)、烟酰胺腺嘌呤二核苷酸四唑还原酶(NADH-TR)、琥珀酸脱氢酶(SDH)染色及免疫组化等常规染色方法进行评估。免疫荧光结果显示,与正常情况相比,在结蛋白病患者或结蛋白病大鼠模型的肌纤维结蛋白高染色区域中VDAC1聚集。同时,凋亡相关蛋白bax和激活转录因子2(ATF2)在结蛋白病患者和结蛋白病大鼠模型中存在,但bcl-2、bcl-xl或己糖激酶2(HK2)不存在。在结蛋白病患者和患结蛋白病大鼠的组织切片中,VDAC1和结蛋白在蛋白水平上密切相关。此外,凋亡蛋白也参与了结蛋白病,如bax、ATF2,但不包括bcl-2、bcl-xl或HK2。该病理分析揭示了VDAC1与结蛋白之间的相关性,且凋亡相关蛋白在结蛋白病中存在相关性。此外,我们为研究结蛋白相关肌病提供了结蛋白病大鼠模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aac8/5152834/f271225b22e6/pone.0167908.g001.jpg

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