...
首页> 外文期刊>Folia neuropathologica >Administration of leukemia inhibitory factor increases Opalin and myelin oligodendrocyte glycoprotein expression in the cerebral cortex in a cuprizone-induced model of demyelination
【24h】

Administration of leukemia inhibitory factor increases Opalin and myelin oligodendrocyte glycoprotein expression in the cerebral cortex in a cuprizone-induced model of demyelination

机译:白血病抑制因子的给药在cuprizone诱导的脱髓鞘模型中增加大脑皮质中的蛋白石和髓磷脂少突胶质细胞糖蛋白表达

获取原文
获取原文并翻译 | 示例

摘要

Multiple sclerosis (ms) lesions are characterized by inflammatory demyelination and reactive gliosis, and although remyelination occurs in some lesions it is limited and incomplete. Leukemia inhibitory factor (LIF) is an important cytokine that stimulates oligodendrocyte proliferation and survival in vitro. Opalin is a unique molecular marker for mature oligodendrocytes. The aim of this study was to demonstrate the role of LIF on Opalin and myelin oligodendrocyte glycoprotein (MOG) expression in the cerebral cortex of cuprizone-induced MS mice. The mice were treated with cuprizone for five weeks in order to induce MS. The mice were then divided into 3 groups. The first group was injected intraperitoneally (IP) with LIF for six weeks in the amount of 30 mu g/kg bw per day. The second group (SHAM) was injected IP with normal saline and the third group was left without injection as a control. After six weeks the mice were killed, the cerebral cortex was harvested, and the expression of MOG and Opalin was studied. Using western blotting we found that LIF increases Opalin and MOG expression in the cerebral cortex extracts as compared to SHAM and control groups. However, no significant difference in the Opalin and MOG expression was seen between SHAM and control groups. It is concluded that LIF may have an important role in the process of remyelination by increasing Opalin expression and MOG expression.
机译:多发性硬化症(ms)病变的特征是炎症性脱髓鞘和反应性神经胶质增生,尽管在某些病变中发生髓鞘再生,但局限性且不完全。白血病抑制因子(LIF)是一种重要的细胞因子,可刺激少突胶质细胞的增殖和体外存活。蛋白石是成熟少突胶质细胞的独特分子标记。这项研究的目的是证明LIF对cuprizone诱导的MS小鼠大脑皮质中的蛋白石和髓磷脂少突胶质细胞糖蛋白(MOG)表达的作用。为了诱导MS,用铜酮治疗小鼠五周。然后将小鼠分为3组。第一组腹膜内(IP)注射LIF,持续六周,每天30毫克/千克体重。第二组(SHAM)腹腔注射生理盐水,第三组不注射作为对照。六周后处死小鼠,收获大脑皮层,并研究MOG和蛋白石的表达。使用蛋白质印迹,我们发现与SHAM和对照组相比,LIF增加了大脑皮层提取物中Opalin和MOG的表达。但是,SHAM与对照组之间的蛋白石和MOG表达没有显着差异。结论是,LIF可能通过增加Opalin表达和MOG表达而在髓鞘再生过程中发挥重要作用。

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