Differential regulation of aldose reductase expression during macrophage polarization depends on hyperglycemia:

Innate Immunity

ChristianErbel¹ 

关键词: Atherosclerosis;    coronary artery disease;    macrophage;    diabetes mellitus;    aldose reductase;   

DOI  :  10.1177/1753425916632053

学科分类：生物科学（综合）

来源: Sage Journals

【 摘 要 】

Aldose reductase (AR; gene AKR1B1) is the rate-limiting enzyme of the polyol pathway and has been associated with diabetes and atherosclerosis. Here, we sought to identify the mechanisms underlying differential AR expression in human atherosclerotic plaque macrophages. In vitro, M1-polarized human monocyte-derived macrophages expressed significantly higher levels of AKR1B1 mRNA and AR protein compared with M2-polarized macrophages. AR activity was significantly higher in M1 macrophages. AKR1B1 mRNA expression correlated positively with the M1 marker TNF (r = 0.430, P = 0.006) and negatively with the M2 marker MRC1 (r = −0.443, P = 0.044). Increased AR expression in M1 macrophages depended on hyperglycemia. Concomitantly, expression of SLC2A1 (coding for the Glc transporter GLUT-1) was significantly higher in M1 than in M2 macrophages. Pharmacological inhibition of GLUT-1 using STF-32 completely abrogated Glc-induced AR up-regulation in M1 macrophages. When analyzing AR expression in post-mortem coronary a...

【 授权许可】

CC BY