Role of HMGB1 signaling in the inflammatory process in diabetic retinopathy

被引:44
作者
Steinle, Jena J. [1 ]
机构
[1] Wayne State Univ, Sch Med, Dept Ophthalmol Visual & Anat Sci, Detroit, MI 48202 USA
关键词
HMGB1; Diabetic retinopathy; TLR4; RAGE; Inflammation; NF-KAPPA-B; GLYCATION END-PRODUCTS; GROUP BOX-1 PROTEIN; OXIDATIVE STRESS; RECEPTOR TLR; HIGH GLUCOSE; RAGE; ACTIVATION; CELLS; PATHWAY;
D O I
10.1016/j.cellsig.2020.109687
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
High mobility group box 1 (HMGB1) is a key player in retinal inflammation. HMGB1 is a danger associated protein pattern receptor which can sense high glucose as a stressor. Increased HMGB1 levels have been found in patients with late stage diabetic retinopathy. HMGB1 can bind toll-like receptor 4 (TLR4) and the receptor for advanced glycation end-products (RAGE), leading to increased inflammation commonly through nuclear factor kappa beta (NFkB). Because diabetic patients have been found to have increased HMGB1 and RAGE levels, as well as polymorphisms of TLR4, a number of investigations have focused on inhibition of these pathways in the diabetic retina. Work in diabetic animal models and cell culture have demonstrated a number of factors that can inhibit HMGB1/TLR4/RAGE signaling. This regulation offers potential new avenues for therapeutic development. This review is focused on HMGB1 signaling and downstream pathways leading to inflammation in the diabetic retina.
引用
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页数:4
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