Galectin-1 attenuates astrogliosis-associated injuries and improves recovery of rats following focal cerebral ischemia

被引:36
|
作者
Qu, Wen-Sheng [1 ]
Wang, Yi-Hui [1 ]
Ma, Jun-Fang [1 ]
Tian, Dai-Shi [1 ]
Zhang, Qiang [1 ]
Pan, Deng-Ji [1 ]
Yu, Zhi-Yuan [1 ]
Xie, Min-Jie [1 ]
Wang, Jian-Ping [2 ]
Wang, Wei [1 ]
机构
[1] Huazhong Univ Sci & Technol, Dept Neurol, Tongji Hosp, Tongji Med Coll, Wuhan 430074, Peoples R China
[2] Zhengzhou Univ, Dept Neurol, Affiliated Hosp 5, Zhengzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
astrogliosis; cerebral ischemia; function recovery; galectin-1; neuronal apoptosis; CYCLE PROTEIN EXPRESSION; INDUCED PROLIFERATION; NEUROPROTECTIVE ROLE; AXONAL REGENERATION; FUNCTIONAL RECOVERY; BRAIN ISCHEMIA; SCAR FORMATION; CELL-DEATH; IN-VITRO; ASTROCYTES;
D O I
10.1111/j.1471-4159.2010.07095.x
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
P>Astrogliosis occurs after brain ischemia, and excessive astrogliosis can devastate the neuronal recovery. Previous reports show that galectin-1 (Gal-1) regulates proliferation of several cell types and plays an important role after nervous system injuries. Here, we found that expression of Gal-1 was remarkably up-regulated in activated astrocytes around ischemic infarct. Furthermore, under ischemic conditions either in vitro or in vivo, Gal-1 was found to inhibit the proliferation of astrocytes in a dose-dependent manner, attenuate astrogliosis and down-regulate the astrogliosis associated expression of nitric oxide synthase and interleukin-1 beta after the ischemia. All these changes were blocked by lactose, suggesting a lectin dependent manner of Gal-1's function. Moreover, 7-day Gal-1 treatment reduced apoptosis of neurons, decreased brain infarction volume and improved neurological function induced by the ischemia. Together, these findings indicate that through reducing astrogliosis related damages, Gal-1 is a potential therapeutical target for attenuating neuronal damage and promoting recovery of brain ischemia.
引用
收藏
页码:217 / 226
页数:10
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