Reduced cerebral ischemia-reperfusion injury in Toll-like receptor 4 deficient mice

被引:218
作者
Cao, Can-xiang
Yang, Qing-wu
Lv, Feng-lin
Cu, Jie
Fu, Hua-bin
Wang, Jing-zhou
机构
[1] Third Mil Med Univ, DaPing Hosp, Dept Neurol, Chongqing 400042, Peoples R China
[2] Third Mil Med Univ, Inst Surg, State Key Lab Trauma Burn & Combined Wound, Chongqing 400042, Peoples R China
关键词
toll-like receptor 4; cerebral ischemia/reperfusion; inflammatory factor; stroke;
D O I
10.1016/j.bbrc.2006.12.057
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
Inflammatory reaction plays an important role in cerebral ischemia-reperfusion injury, however, its mechanism is still unclear. Our study aims to explore the function of Toll-like receptor 4 (TLR4) in the process of cerebral ischemia-reperfusion. We made middle cerebral artery ischemia-reperfusion model in mice with line embolism method. Compared with C3H/OuJ mice, scores of cerebral water content, cerebral infarct size and neurologic impairment in C3H/Hej mice were obviously lower after 6 h ischemia and 24 h reperfusion. Light microscopic and electron microscopic results showed that cerebral ischemia-reperfusion injury in C3H/Hej mice was less serious than that in C3H/OuJ mice. TNF-alpha and IL-6 contents in C3H/HeJ mice were obviously lower than that in C3H/OuJ mice with ELISA. The results showed that TLR4 participates in the process of cerebral ischemia-reperfusion injury probably through decrease of inflammatory cytokines. TLR4 may become a new target for prevention of cerebral ischemia-reperfusion injury. Our study suggests that TLR4 is one of the mechanisms of cerebral ischemia-reperfusion injury besides its important role in innate immunity. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:509 / 514
页数:6
相关论文
共 32 条
[1]  
ANDREM A, 2000, NATURE, V406, P782
[2]   Toll-like receptor 4 on nonhematopoietic cells sustains CNS inflammation during endotoxemia, independent of systemic cytokines [J].
Chakravarty, S ;
Herkenham, M .
JOURNAL OF NEUROSCIENCE, 2005, 25 (07) :1788-1796
[3]   Inflammatory mechanisms after ischemia and stroke [J].
Danton, GH ;
Dietrich, WD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2003, 62 (02) :127-136
[4]  
Felberg R A, 2000, CNS Spectr, V5, P52
[5]   Acute Stroke Pathophysiology, Diagnosis, and Treatment [J].
Frizzell, Joan Parker .
AACN ADVANCED CRITICAL CARE, 2005, 16 (04) :421-440
[6]   Treatment and secondary prevention of stroke: evidence, costs, and effects on individuals and populations [J].
Hankey, GJ ;
Warlow, CI .
LANCET, 1999, 354 (9188) :1457-1463
[7]   Inflammation in stroke and focal cerebral ischemia [J].
Huang, Judy ;
Upadhyay, Urvashi A. ;
Tamargo, Rafael J. .
SURGICAL NEUROLOGY, 2006, 66 (03) :232-245
[8]   Reperfusion injury after focal cerebral ischemia: The role of inflammation and the therapeutic horizon [J].
Jean, WC ;
Spellman, SR ;
Nussbaum, ES ;
Low, WC .
NEUROSURGERY, 1998, 43 (06) :1382-1396
[9]   Receptor-mediated monitoring of tissue well-being via detection of soluble heparan sulfate by toll-like receptor 4 [J].
Johnson, GB ;
Brunn, GJ ;
Kodaira, Y ;
Platt, JL .
JOURNAL OF IMMUNOLOGY, 2002, 168 (10) :5233-5239
[10]  
Jorgensen HS, 1999, CLIN GERIATR MED, V15, P785