ROCK mediates the inflammatory response in thrombin induced microglia

•Increased expression of ROCK, NO and TNF-α in thrombin induced microglia was found.•Enhanced phagocytosis in thrombin induced microglia was also found.•Argatroban or Y-27632 pretreatment decreased ROCK, NO and TNF-α expression.•Argatroban or Y-27632 pretreatment reduced phagocytosis in thrombin ind...

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Veröffentlicht in:Neuroscience letters 2013-10, Vol.554, p.82-87
Hauptverfasser: Cui, Guiyun, Zuo, Tao, Zhao, Qiuchen, Hu, Jinxia, Jin, Peisheng, Zhao, Hui, Jing, Jia, Zhu, Jienan, Chen, Hao, Liu, Bin, Hua, Fang, Ye, Xinchun
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Sprache:eng
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Zusammenfassung:•Increased expression of ROCK, NO and TNF-α in thrombin induced microglia was found.•Enhanced phagocytosis in thrombin induced microglia was also found.•Argatroban or Y-27632 pretreatment decreased ROCK, NO and TNF-α expression.•Argatroban or Y-27632 pretreatment reduced phagocytosis in thrombin induced microglia.•ROCK may regulate the inflammatory response in thrombin induced microglia. To investigate whether the ROCK pathway is involved in thrombin-induced microglial inflammatory response, thrombin-induced microglia were pretreated with the thrombin inhibitor argatroban or a ROCK inhibitor Y-27632. Microglial inflammatory response was evaluated by phagocytosis of fluorescein labeled latex beads analyses and inflammatory mediators’ expression such as nitric oxide (NO) and tumor necrosis factor-alpha (TNF-а). Compared to non-induced microglia, thrombin-induced microglia show significantly enhanced phagocytotic capacity and increased ROCK, NO and TNF-а expression. Pretreatment of thrombin-induced microglia with argatroban or Y-27632 significantly decreased phagocytotic capacity and reduced ROCK, NO and TNF-α expression. Therefore, the ROCK pathway may play a vital role in the mechanisms by which thrombin induces microglia in the inflammatory response.
ISSN:0304-3940
1872-7972
DOI:10.1016/j.neulet.2013.08.065