Electroacupuncture prevents LPS- induced neuroinflammation via upregulation of PICK-TLR4 complexes in the microglia of hippocampus

TLR4型 神经炎症 小胶质细胞 促炎细胞因子 p38丝裂原活化蛋白激酶 电针 海马体 MAPK/ERK通路 下调和上调 神经科学 化学 医学 信号转导 炎症 免疫学 生物 生物化学 病理 基因 替代医学 针灸科
作者
Yunchang Mo,Lu Wang,Miao Ren,Wenjing Xie,Xiaoxiao Ye,Bingbing Zhou,Anqi Zhang,Qinxue Dai,Junlu Wang
出处
期刊:Brain Research Bulletin [Elsevier]
卷期号:177: 295-304 被引量:11
标识
DOI:10.1016/j.brainresbull.2021.10.010
摘要

Sepsis-associated encephalopathy (SAE) is a common complication of sepsis caused by neuroinflammation. Electroacupuncture (EA) can be used to treat SAE, but the underlying mechanism is not clear. Lack of PICK1 further aggravates the inflammatory response in mice with sepsis. Therefore, we sought to investigate whether PICK1 is involved in the protective effects of electroacupuncture to SAE. In this study, mice were treated with EA after lipopolysaccharide (LPS) treatment. Behavioral tests; microglial activity of hippocampus; neuron survival and the inflammatory factors PICK1 and TLR4, as well as TLR4-related proteins, such as ERK, JNK, and P38, were assessed after EA treatment. PICK1, TLR4, and TLR4-related proteins, as well as PICK1-TLR4 complex levels were assessed in BV2 cells treated with LPS, PICK1 siRNA, or PICK1 polypeptide. The results indicated that EA could improve neurological assessment and reduce activation of microglial and TLR4 and expression of proinflammatory cytokines. EA also reduced the expression of TLR4 and phosphorylation of ERK/JNK/P38 while, increased the expression of PICK1 and TLR4 complexes. PICK1 knockdown further promoted the expression of TLR4 and phosphorylation of ERK/JNK/P38 in BV2 cells, but this effect was reversed by PICK1 polypeptides. These results suggest that EA may reduce neuroinflammation responses, decrease inflammatory factors, and finally, protect SAE by increasing the formation of PICK1-TLR4 complexes in microglia.
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