Microglial LOX-1/MAPKs/NF-κB positive loop promotes the vicious cycle of neuroinflammation and neural injury

被引:22
|
作者
Ge, Xin [1 ,2 ]
Zhang, Dong-Mei [1 ]
Li, Meng-Meng [1 ,2 ]
Zhang, Yi [3 ]
Zhu, Xiang-Yang [4 ]
Zhou, Yong [4 ]
Peng, Xiao [1 ]
Shen, Ai-Guo [1 ,2 ,5 ]
机构
[1] Nantong Univ, Clin Med Res Ctr, Affiliated Hosp 2, Nantong 226001, Peoples R China
[2] Nantong Univ, Jiangsu Key Lab Neurogenerat, Nantong 226001, Peoples R China
[3] Nantong Univ, Neurosurg Dept, Affiliated Hosp 2, Nantong 226001, Peoples R China
[4] Nantong Univ, Neurol Dept, Affiliated Hosp 2, Nantong 226001, Peoples R China
[5] Nantong Univ, Canc Res Ctr Nantong, Tumor Hosp, Nantong 226361, Peoples R China
基金
中国国家自然科学基金;
关键词
LOX-1; Neuroinflammation; Microglia activation; Neural injury; MAPK; NF-kappa B; DENSITY-LIPOPROTEIN RECEPTOR-1; INDUCED LOX-1 EXPRESSION; ENDOTHELIAL-CELLS; DOWN-REGULATION; ATHEROSCLEROSIS; ACTIVATION; APOPTOSIS; MACROPHAGES; MODULATION; PATHWAY;
D O I
10.1016/j.intimp.2019.02.013
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1), a member of the scavenger receptor family, recognizes multiple ligands and participates in several inflammatory responses, but its function within the central nervous system (CNS) remains unclear. In this study, we discovered an increased LOX-1 expression in activated microglia in vivo and in vitro. Employing the specific inhibitors, we found that conditioned medium of necrotic neurons (Necrotic-CM) induced microglial LOX-1 expression through the MAPKs/NF-kappa B pathway. Silencing LOX-1 inhibited MAPK phosphorylation, NF-kappa B-p65 nuclear transportation, and pro-inflammatory factor production in microglia exposed to Necrotic-CM. Furthermore, utilizing the conditioned medium of activated microglia (MG-CM), we discovered microglial LOX-1 aggravated the neuroinflammation-induced neuronal apoptosis. Collectively, a LOX-1/MPAKs/NF-kappa B positive loop might promote microglia activation and drive the vicious cycle of neuroinflammation and neuronal injury.
引用
收藏
页码:187 / 200
页数:14
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