Differential pro-inflammatory responses of TNF-α receptors (TNFR1 and TNFR2) on LOX-1 signalling

被引:15
作者
Arjuman, Albina [1 ]
Chandra, Nimai C. [1 ]
机构
[1] AIIMS, Dept Biochem, New Delhi 110029, India
关键词
LOX-1; TNF receptors; Atherosclerosis; Nitric oxide; Oxidized-LDL; LOW-DENSITY-LIPOPROTEIN; LECTIN-LIKE; EXPRESSION; ATHEROSCLEROSIS; MACROPHAGES; IDENTIFICATION;
D O I
10.1007/s11033-014-3841-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
TNF-alpha potently induces LOX-1 expression in THP-1 macrophages at concentrations between 1.25-50 ng/mL. The interplay between the two TNF receptors (TNFR1 and TNFR2) was apparent in the expression pattern of LOX-1 in response to TNF-alpha. Interestingly, R1 signal abrogation depleted both TNFR2 as well as LOX-1 transcript expression, suggesting that TNFR1 holds priority in the relative signaling mechanism between TNFR1 and TNFR2. TNF-alpha was also found to abrogate the oxidized-LDL (ox-LDL) mediated increase in intracellular pool of NO, a known downstream intermediate of LOX-1 pro-inflammatory signaling cascade. At the level of ox-LDL clearance, TNF-alpha inhibited the uptake (scavenging) of ox-LDL via LOX-1. Our study demonstrates the ability of TNF-alpha to enhance the signaling propensity of LOX-1 by increasing its expression and inhibiting its scavenging property.
引用
收藏
页码:1039 / 1047
页数:9
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