特雷姆2
炎症体
粒体自噬
帕金
术后认知功能障碍
炎症
神经保护
医学
下调和上调
药理学
麻醉
免疫学
内科学
内分泌学
小胶质细胞
神经科学
心理学
认知
化学
生物化学
细胞凋亡
自噬
疾病
帕金森病
基因
作者
Wenwen Jiang,Fang Liu,Hongqing Li,Kexin Wang,Xuezhao Cao,Xiaohan Xu,Yongjian Zhou,Jie Zou,Xinyue Zhang,Xiaotong Cui
标识
DOI:10.1016/j.neuro.2022.04.005
摘要
Postoperative cognitive dysfunction (POCD) is a major postoperative complication. Triggering receptor expressed on myeloid cells 2 (TREM2) exerts a neuroprotective function against neuro-inflammatory responses. The present study investigated the role of TREM2 in anesthesia and surgery-induced cognitive impairment and the potential related mechanism. Our results revealed that TREM2 was downregulated, coupled with activation of the NLRP3 inflammasome and subsequent IL-1β expression on postoperative day 3. A corresponding decline in PSD-95 and BDNF was found at the same time point. The key regulator of mitophagy PINK1 and Parkin protein levels were significantly decreased following surgery and anesthesia. TREM2 overexpression partially reversed postoperative cognitive impairment and enhanced PSD-95 and BDNF expression. TREM2 overexpression also improved mitophagy function and inhibited activation of the NLRP3 inflammasome and associated production of IL-1β. Our findings demonstrate that TREM2 rescues anesthesia and surgery-induced spatial learning and memory impairment and neuro-inflammation in aged C57/BL6 mice, which may be at least partially mediated through the activation of mitophagy and subsequent inhibition of the NLRP3 inflammasome.
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