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[神经毒性因子与多发性硬化症]

[Gliotoxic factor and multiple sclerosis].

作者信息

Rieger F, Amouri R, Benjelloun N, Cifuentes-Diaz C, Lyon-Caen O, Hantaz-Ambroise D, Dobransky T, Perron H, Gemy C

机构信息

INSERM U. 153, équipe de neurobiologie et de neuropathologie fondamentales, Paris, France.

出版信息

C R Acad Sci III. 1996 Apr;319(4):343-50.

PMID:8762982
Abstract

Multiple sclerosis in a disease of the central nervous system characterized by perivascular and periventricular lesions of the myelin and immune cell infiltrates and increased permeability of the blood-brain barrier. We have found a cytotoxic factor of the cerebrospinal fluid (CSF) specific for multiple sclerosis patients which has 2 main characteristic effects in vitro on primary or immortalized astrocyte cultures: (1) disruption of the gliofilament network of the cells; and (2) apoptotic cell death induction. Moreover, in vivo, intraventricular injections of minute amounts of partially purified gliotoxic factor in adult rats have striking effects on both the morphology and general organization of astrocytes in the entire brain and the permeability characteristics of the blood brain barrier, which becomes leaky to immunoglobulins. These pathological effects are strongly similar to some of the neuropathological findings reported during the course of MS--They suggest an entirely new hypothesis to explain the active stage of the disease: the presence of a new factor of unknown extrinsic (viral) or intrinsic (cellular) origin, able to disorganize the glial cytoskeleton and glial cell differentiation. This factor is then able to provoke glial cell death. Such glial cell death may result in both demyelination and increased blood brain barrier permeability. Both in vitro and in vivo studies strongly support the idea that this gliotoxic factor plays a central role in the pathogenesis of MS, making its full identification a critical theme for MS research.

摘要

多发性硬化症是一种中枢神经系统疾病,其特征为髓鞘的血管周围和脑室周围病变、免疫细胞浸润以及血脑屏障通透性增加。我们发现了一种针对多发性硬化症患者的脑脊液(CSF)细胞毒性因子,该因子在体外对原代或永生化星形胶质细胞培养物有两个主要特征性作用:(1)破坏细胞的神经胶质丝网络;(2)诱导细胞凋亡。此外,在体内,向成年大鼠脑室内注射微量部分纯化的神经胶质毒性因子,会对整个大脑中星形胶质细胞的形态和整体组织结构以及血脑屏障的通透性特征产生显著影响,血脑屏障会对免疫球蛋白变得渗漏。这些病理效应与多发性硬化症病程中报道的一些神经病理学发现非常相似——它们提出了一个全新的假说来解释该疾病的活动期:存在一种未知的外在(病毒)或内在(细胞)来源的新因子,能够破坏神经胶质细胞骨架和神经胶质细胞分化。然后这种因子能够引发神经胶质细胞死亡。这种神经胶质细胞死亡可能导致脱髓鞘和血脑屏障通透性增加。体外和体内研究都有力地支持了这样一种观点,即这种神经胶质毒性因子在多发性硬化症的发病机制中起核心作用,因此对其进行全面鉴定是多发性硬化症研究的一个关键课题。

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