Author:
Broch M,Ramírez R,Auguet M T,Alcaide M J,Aguilar C,Garcia-España A,Richart C
Abstract
Obesity is linked to a low-level chronic inflammatory state that
may contribute to the development of associated metabolic
complications. Retinol-binding protein 4 (RBP4) is an adipokine
associated with parameters of obesity including insulin resistance
indices, body mass index, waist circumference, lipid profile, and
recently, with circulating inflammatory factors. Due to the
infiltration of adipose tissue in obesity by macrophages derived
from circulating monocytes and, on the other hand, the existence
of a close genetic relationship between adipocytes and
macrophages, we decided to examine if RBP4 is expressed in
monocytes and/or primary human macrophages. While we did
not detect expression of RBP4 in undifferentiated monocytes,
RBP4 expression became evident during the differentiation of
monocytes into macrophages and was highest in differentiated
macrophages. Once we demonstrated the expression of RBP4 in
macrophages, we checked if RBP4 expression could be regulated
by inflammatory stimuli such as tumor necrosis factor-alpha
(TNF-α), interleukin-6 (IL-6), or the endotoxin lipopolysaccharide
(LPS). We observed that while RBP4 expression was strongly
inhibited by TNF-α and LPS, it was not affected by IL-6. Our
results highlight the complexity behind the regulation of this
adipokine and demonstrate that RBP4 expression in macrophages
could be modulated by inflammatory stimuli.
Publisher
Institute of Physiology of the Czech Academy of Sciences
Subject
General Medicine,Physiology
Cited by
44 articles.
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