首页> 美国卫生研究院文献>Cerebrospinal Fluid Research >Differential cytokine expression by brain microglia/macrophages in primary culture after oxygen glucose deprivation and their protective effects on astrocytes during anoxia
【2h】

Differential cytokine expression by brain microglia/macrophages in primary culture after oxygen glucose deprivation and their protective effects on astrocytes during anoxia

机译:缺氧后脑小胶质细胞/巨噬细胞在原代培养中差异表达的细胞因子及其对星形胶质细胞的保护作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BackgroundActivation of microglia/macrophages following cerebral ischemia may be beneficial or detrimental for the survival of brain cells, an ambiguity in effects that has been explained by findings that ischemia can induce transformation of resting monocytes/macrophages into two different inflammation-related phenotypes, termed M1 and M2. The extent to which this differentiation depends on paracrine signaling from other brain cells is not clear. This study explored if oxygen glucose deprivation (OGD) can trigger expression of phenotype-specific markers in rat microglia/macrophages in primary culture, in absence/low abundance of other brain cells. Time pattern of these changes was assessed and compared to time-pattern that has been revealed in vivo previously. Effects of phenotype-specific cytokines on viability of astrocytes in primary culture during anoxia were also explored.
机译:背景脑缺血后小胶质细胞/巨噬细胞的激活可能对脑细胞的存活有益或有害,这一发现的歧义已被以下发现所解释:缺血可诱导静息单核细胞/巨噬细胞转化为两种不同的炎症相关表型,称为M1。和M2。这种分化依赖于其他脑细胞旁分泌信号传导的程度尚不清楚。这项研究探讨了在缺乏/低其他脑细胞丰度的情况下,缺氧葡萄糖剥夺(OGD)是否可以触发大鼠小胶质细胞/巨噬细胞中表型特异性标志物的表达。评估了这些变化的时间模式,并将其与之前体内发现的时间模式进行了比较。还探讨了表型特异性细胞因子对缺氧时原代培养中星形胶质细胞活力的影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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