The IFN-β and retinoic acid-induced cell death regulator GRIM-19 is upregulated during focal cerebral ischemia

被引:15
|
作者
Mehrabian, Zara
Chandrasekaran, Krish
Kalakonda, Sudhakar
Kristian, Tibor
Fiskum, Gary
Kalvakolanu, Dhananjaya V.
机构
[1] Univ Maryland, Sch Med, Dept Anesthesiol, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Microbiol & Immunol, Baltimore, MD 21201 USA
来源
关键词
D O I
10.1089/jir.2006.0067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The induction of GRIM-19 has been shown to be essential for interferon-beta (IFN-beta)-induced and retinoic acid (RA)- induced tumor cell death. We have studied the localization and levels of GRIM-19 in IFN/RA-induced cell death in neural cells and in focal cerebral ischemia. Exposure to IFN/RA caused a similar to 15-fold increase in GRIM-19 protein levels and induced similar to 50% cell death in human neuroblastoma SH-SY5Y cells. In rats subjected to permanent focal cerebral ischemia, increased oxidative stress, as well as increased GRIM mRNA levels (32-fold) and increased GRIM-19 (> 50%) protein levels were noted in the ipsilateral (affected) hemisphere compared with the contralateral (unaffected) hemisphere. These results suggest that GRIM-19 may play a role in ischemia-induced neuronal cell death.
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收藏
页码:383 / 391
页数:9
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