Toll-like receptor 4 and protease-activated receptor 2 in physiology and pathophysiology of the nervous system: more than just receptor cooperation?

被引:20
作者
Widera, Darius [1 ]
Martinez Aguilar, Rocio [1 ,2 ]
Cottrell, Graeme S. [3 ]
机构
[1] Univ Reading, Sch Pharm, Stem Cell Biol & Regenerat Med Grp, Whiteknights Campus, Reading, Berks, England
[2] Univ Granada, IBIMER, Unidad Inmunol, Granada, Spain
[3] Univ Reading, Sch Pharm, Cellular & Mol Neurosci, Reading, Berks, England
关键词
signaling; inflammation; proteases; myeloid of differentiation primary response gene 88; TIR-domain containing adaptor inducing interferon; lipopolysaccharide; TLR4; PAR2; ARRESTIN-DEPENDENT ENDOCYTOSIS; NF-KAPPA-B; SIGNAL-TRANSDUCTION; UP-REGULATION; TLR4; PAR2; LPS; PROTEINASE-ACTIVATED-RECEPTOR-2; INFLAMMATION; STIMULATION;
D O I
10.4103/1673-5374.251290
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Toll-like receptor 4 (TLR4) and protease-activated receptor 2 (PAR2) play pivotal roles in the mammalian innate immune response. Notably, in addition to their involvement in detection of invading pathogens, PAR2 and TLR4 modulate the levels of cell death-induced sterile inflammation by activating pro- or anti-inflammatory downstream signaling cascades. Within the central nervous system, there is emerging evidence that both receptors are involved in synaptic transmission and brain plasticity. Furthermore, due to their prominent role in mediating neuroinflammation, PAR2 and TLR4 are associated with development and progression of neurodegenerative disorders including but not limited to Alzheimer's disease, Parkinson's disease and multiple sclerosis. In this article, we summarise the current knowledge on the cooperation between PAR2 and TLR4, discuss the potential cross-talk levels and highlight the impact of the cross-coupling on neuroinflammation.
引用
收藏
页码:1196 / 1201
页数:6
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