首页> 外文期刊>Experimental Neurology >Live imaging of remyelination after antibody-mediated demyelination in an ex-vivo model for immune mediated CNS damage.
【24h】

Live imaging of remyelination after antibody-mediated demyelination in an ex-vivo model for immune mediated CNS damage.

机译:在免疫介导的中枢神经系统损伤的体外模型中,抗体介导的脱髓鞘后的实时髓鞘成像。

获取原文
获取原文并翻译 | 示例
           

摘要

Mononuclear cell infiltrates, deposits of immunoglobulin and complement as well as demyelination and axonal damage are neuropathological hallmarks of Multiple Sclerosis (MS) lesions. An involvement of antibodies is further suggested by the presence of oligoclonal immunoglobulins in the cerebrospinal fluid of almost all MS patients. However, which mechanisms are most relevant for de- and remyelination and axonal loss in MS lesions is poorly understood. To characterize the regenerative abilities of demyelinated CNS tissue, we utilized murine organotypic cerebellar slice cultures expressing GFP in oligodendrocytes. The addition of a demyelinating monoclonal antibody specific for myelin oligodendrocyte glycoprotein and complement induced complete myelin destruction and oligodendrocyte loss, as demonstrated by confocal live imaging and staining for different myelin proteins. After removal of antibodies and complement we visualized the stages of remyelination, presumably originating from proliferating oligodendrocyte precursor cells and guided by morphologically intact appearing axons. Allowing for the detailed live imaging of de- and remyelination in an ex vivo situation closely resembling the three dimensional cytoarchitecture of the CNS, we provide a useful experimental system for the evaluation of new therapeutic strategies to enhance remyelination and repair in MS.
机译:单核细胞浸润,免疫球蛋白和补体的沉积以及脱髓鞘和轴突损伤是多发性硬化症(MS)病变的神经病理学标志。几乎所有MS患者的脑脊液中都存在寡克隆免疫球蛋白,这进一步暗示了抗体的参与。然而,对于MS病变中的脱髓鞘和髓鞘再生以及轴突丧失最相关的机制了解甚少。为了表征脱髓鞘的中枢神经系统组织的再生能力,我们利用在少突胶质细胞中表达GFP的小鼠器官型小脑切片培养物。通过共聚焦实时成像和不同髓磷脂蛋白染色证明,添加了对髓磷脂少突胶质细胞糖蛋白和补体特异的脱髓鞘单克隆抗体,可诱导髓磷脂的完全破坏和少突胶质细胞的丢失。去除抗体和补体后,我们观察到髓鞘再生的阶段,大概是起源于少突胶质细胞前体细胞的增殖,并受到形态完整的轴突的引导。允许在离体情况下进行脱髓鞘和髓鞘再生的详细实时成像,非常类似于CNS的三维细胞结构,我们提供了一个有用的实验系统,用于评估增强MS的髓鞘再生和修复的新治疗策略。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号