TY - JOUR
T1 - Surgery-induced cognitive dysfunction is alleviated through triggering receptor expressed on myeloid cells 2
AU - Niu, Wen
AU - Ma, Lei
AU - Tao, Tianqi
AU - Tian, Fangfang
AU - He, Tao
AU - Qiao, Min
AU - He, Haimeng
AU - Liu, Xiuhua
AU - Zhao, Xiayong
N1 - Publisher Copyright:
© 2020 Elsevier GmbH
PY - 2020/7
Y1 - 2020/7
N2 - Neuroinflammation plays a key role in perioperative neurocognitive disorders (PND). Increased evidences indicate that triggering receptor expressed on myeloid cells 2 (TREM2) can mitigate inflammatory response in the brain, and the aim of this study is to investigate whether TREM2 is involved in surgery-induced cognitive dysfunction in adult mice. We used adult C57BL/6 mice subjected to intramedullary fixation surgery, and found that surgery did not impair the motor ability of mice, but worsened the learning and memory function, and reduced the expression of TREM2. Meanwhile, up-regulated TREM2 expression in the brain of mice, induced by selective TREM2 agonist HSP60, significantly improved the learning and memory, alleviated the neuroinflammation, and decreased the neuronal cell apoptosis in mice. Meanwhile, TREM2-siRNA abolished the increased expression of TREM2 induced by HSP60, and reversed all the HSP60-induced beneficial effects. Therefore, our study indicated that up-regulation of TREM2 alleviated neuroinflammation and improved learning and memory function after surgery in mice.
AB - Neuroinflammation plays a key role in perioperative neurocognitive disorders (PND). Increased evidences indicate that triggering receptor expressed on myeloid cells 2 (TREM2) can mitigate inflammatory response in the brain, and the aim of this study is to investigate whether TREM2 is involved in surgery-induced cognitive dysfunction in adult mice. We used adult C57BL/6 mice subjected to intramedullary fixation surgery, and found that surgery did not impair the motor ability of mice, but worsened the learning and memory function, and reduced the expression of TREM2. Meanwhile, up-regulated TREM2 expression in the brain of mice, induced by selective TREM2 agonist HSP60, significantly improved the learning and memory, alleviated the neuroinflammation, and decreased the neuronal cell apoptosis in mice. Meanwhile, TREM2-siRNA abolished the increased expression of TREM2 induced by HSP60, and reversed all the HSP60-induced beneficial effects. Therefore, our study indicated that up-regulation of TREM2 alleviated neuroinflammation and improved learning and memory function after surgery in mice.
KW - Neuroinflammation
KW - Perioperative neurocognitive disorders
KW - Triggering receptor expressed on myeloid cells 2
UR - https://www.scopus.com/pages/publications/85084213678
U2 - 10.1016/j.acthis.2020.151553
DO - 10.1016/j.acthis.2020.151553
M3 - 文章
C2 - 32381365
AN - SCOPUS:85084213678
SN - 0065-1281
VL - 122
JO - Acta Histochemica
JF - Acta Histochemica
IS - 5
M1 - 151553
ER -