首页> 美国卫生研究院文献>Cell Death Disease >ALV-J inhibits autophagy through the GADD45β/MEKK4/P38MAPK signaling pathway and mediates apoptosis following autophagy
【2h】

ALV-J inhibits autophagy through the GADD45β/MEKK4/P38MAPK signaling pathway and mediates apoptosis following autophagy

机译:ALV-J通过GADD45β/ M​​EKK4 / P38MAPK信号通路抑制自噬并在自噬之后介导细胞凋亡

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

DF-1 cells were infected with ALV-J for 24, 48, or 72 h and the expression levels of GADD45β were analyzed. Statistical differences were determined using two-way ANOVA.  **  ***  b Following 24, 48, or 72 h of ALV-J infection, total protein was extracted from DF-1 cells or CEF cells, the expression levels of GADD45β were analyzed using western blotting. The chart ( ) shows the quantification of GADD45β/β-actin in ( ). Cells were infected with ALV-J for 24 h and immunostained with rabbit anti-gp37 antibody (green). The expression levels of GADD45β (red) were analyzed using confocal microscopy. DAPI (blue) was used to stain the nuclear DNA. Scale bar, 10 μm. The chart ( ) shows the fluorescence intensity of endogenous GADD45β in ( ). All experiments were repeated in triplicate.
机译:用Alv-j感染DF-1细胞24,48或72小时,分析了GADD45β的表达水平。使用双向ANOVA确定统计差异。 ** ** *** B以下24,48或72小时的Alv-J感染,从DF-1细胞或CEF细胞中提取总蛋白质,使用Western印迹分析GADD45β的表达水平。图表()显示了在()中的Gadd45β/β-actin的定量。将细胞用Alv-J感染24小时,并用兔抗GP37抗体(绿色)免疫染色。使用共聚焦显微镜分析GADD45β(红色)的表达水平。 DAPI(蓝色)用于染色核DNA。秤杆,10μm。图表()显示了()内源性Gadd45β的荧光强度。所有实验均以三份重复。

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