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通过激活未折叠蛋白反应定义的内质网应激在多系统萎缩中的作用。

Involvement of endoplasmic reticulum stress defined by activated unfolded protein response in multiple system atrophy.

机构信息

Department of Neurology, Gunma University Graduate School of Medicine, Gunma, Japan.

出版信息

J Neurol Sci. 2010 Oct 15;297(1-2):60-5. doi: 10.1016/j.jns.2010.06.019. Epub 2010 Jul 29.

Abstract

Multiple system atrophy (MSA) and Parkinson's disease (PD) are classified as synucleinopathies that exhibit α-synuclein deposition in the central nervous system. Recently, activation of the unfolded protein response (UPR), which is a cellular stress response triggered by endoplasmic reticulum (ER) stress, was reported in PD and involvement of ER stress was indicated for this disease. To elucidate whether ER stress is also implicated in the pathology of MSA, we performed a series of immunohistochemical studies using MSA brain sections. Here, we showed the presence of an activated UPR response in oligodendroglia of postmortem MSA brains. The UPR protein-positive structures were observed in lesions where glial cytoplasmic inclusions (GCIs) appeared and colocalized highly in cells showing oligodendrocytic characteristics in the presence of α-synuclein inclusions. The UPR protein-positive structures appeared as granular shapes that are morphologically similar to granulovacuolar degeneration (GVD) and colocalized with GVD marker proteins. Double immunohistochemistry demonstrated that some of the activated UPR protein-positive structures were localized in oligodendrocytes that contained GCIs with faint α-synuclein labeling, without ubiquitination, and showing a strong correlation with the relocation of the tubulin polymerization-promoting protein (TPPP/p25α). These findings suggest that activation of the UPR may be induced at the early stage of the disease process, thus playing a pivotal role in the pathology of MSA.

摘要

多系统萎缩症 (MSA) 和帕金森病 (PD) 被归类为α-突触核蛋白在中枢神经系统中沉积的突触核蛋白病。最近,据报道, unfolded protein response(UPR)的激活,即内质网 (ER) 应激引发的细胞应激反应,在 PD 中存在,并且 ER 应激也与该疾病有关。为了阐明 ER 应激是否也与 MSA 的病理学有关,我们使用 MSA 脑切片进行了一系列免疫组织化学研究。在这里,我们显示了 MSA 脑死后的少突胶质细胞中存在活跃的 UPR 反应。在出现神经胶质细胞质包涵体 (GCIs) 的病变中观察到 UPR 蛋白阳性结构,并且在存在 α-突触核蛋白包涵体的情况下,与具有少突胶质细胞特征的细胞高度共定位。UPR 蛋白阳性结构呈颗粒状,形态上类似于颗粒空泡变性 (GVD),并且与 GVD 标志物蛋白共定位。双重免疫组织化学显示,一些活化的 UPR 蛋白阳性结构定位于含有 GCIs 的少突胶质细胞中,这些 GCIs 具有微弱的 α-突触核蛋白标记、无泛素化,并且与微管聚合促进蛋白 (TPPP/p25α) 的重定位强烈相关。这些发现表明,UPR 的激活可能发生在疾病过程的早期阶段,因此在 MSA 的病理学中发挥关键作用。

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