The two faces of IKK and NF-κB inhibition:: prevention of systemic inflammation but increased local injury following intestinal ischemia-reperfusion

被引:419
作者
Chen, LW
Egan, L
Li, ZW
Greten, FR
Kagnoff, MF
Karin, M [1 ]
机构
[1] Univ Calif San Diego, Dept Pharmacol, Lab Gene Regulat & Signal Transduct, San Diego, CA 92103 USA
[2] Univ Calif San Diego, Dept Med, Lab Mucosal Immun, San Diego, CA 92103 USA
[3] Natl Yang Ming Med Univ, Kaohsiung Vet Gen Hosp, Dept Surg, Taipei, Taiwan
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nm849
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
We studied the role of NF-kappaB in acute inflammation caused by gut ischemia-reperfusion through selective ablation of IkappaB kinase (IKK)-beta, the catalytic subunit of IKK that is essential for NF-kappaB activation. Ablation of IKK-beta in enterocytes prevented the systemic inflammatory response, which culminates in multiple organ dysfunction syndrome (MODS) that is normally triggered by gut ischemia-reperfusion. IKK-beta removal from enterocytes, however, also resulted in severe apoptotic damage to the reperfused intestinal mucosa. These results show the dual function of the NF-kappaB system, which is responsible for both tissue protection and systemic inflammation, and underscore the caution that should be exerted in using NF-kappaB and IKK inhibitors.
引用
收藏
页码:575 / 581
页数:7
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