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脂联素对猪巨噬细胞中的细胞因子有不同的调节作用。

Adiponectin differentially regulates cytokines in porcine macrophages.

作者信息

Wulster-Radcliffe Meghan C, Ajuwon Kolapo M, Wang Jiazhen, Christian John A, Spurlock Michael E

机构信息

Department of Animal Sciences, Comparative Medicine Program, Purdue University, West Lafayette, IN, USA.

出版信息

Biochem Biophys Res Commun. 2004 Apr 9;316(3):924-9. doi: 10.1016/j.bbrc.2004.02.130.

DOI:10.1016/j.bbrc.2004.02.130
PMID:15033490
Abstract

Adiponectin, an adipocyte-derived hormone, attenuates the production of TNFalpha by activated human macrophages. In the present study, we used porcine blood-derived macrophages to test the hypothesis that the anti-inflammatory action of adiponectin includes suppression of IL6 and an induction of IL10. Adiponectin suppressed both TNFalpha and IL6 production in macrophages activated with lipopolysaccharide (P<0.01). In contrast, adiponectin increased IL10 expression (P<0.05) and augmented (P<0.05) the induction of this cytokine by lipopolysaccharide (LPS). Mechanistically, the attenuation of proinflammatory cytokine production by adiponectin was associated with an attenuation of the translocation of NFkappaB to the nucleus. Either adiponectin or inhibition of ERK1/2 with U0126 diminished the induction of IL6 by LPS (P<0.05), but the combination of adiponectin and the inhibitor did not further reduce IL6 production. In contrast, the inhibitory actions of adiponectin and a p38 MAPK inhibitor (SB203580) were additive (P<0.05). These data indicate that the anti-inflammatory actions of adiponectin include suppression of IL6 and induction of IL10. In addition, we provide evidence that some of the anti-inflammatory actions of adiponectin are mediated in part by suppression of NFkappaB signaling and ERK1/2 activity.

摘要

脂联素是一种由脂肪细胞分泌的激素,可减弱活化的人类巨噬细胞产生肿瘤坏死因子α(TNFα)的能力。在本研究中,我们使用猪血来源的巨噬细胞来验证脂联素的抗炎作用包括抑制白细胞介素6(IL6)和诱导白细胞介素10(IL10)这一假设。脂联素可抑制脂多糖激活的巨噬细胞中TNFα和IL6的产生(P<0.01)。相反,脂联素可增加IL10的表达(P<0.05),并增强(P<0.05)脂多糖(LPS)对这种细胞因子的诱导作用。从机制上讲,脂联素对促炎细胞因子产生的减弱与核因子κB(NFκB)向细胞核的转位减弱有关。脂联素或用U0126抑制细胞外信号调节激酶1/2(ERK1/2)均可减少LPS对IL6的诱导(P<0.05),但脂联素与抑制剂联合使用并未进一步降低IL6的产生。相反,脂联素和p38丝裂原活化蛋白激酶抑制剂(SB203580)的抑制作用具有相加性(P<0.05)。这些数据表明脂联素的抗炎作用包括抑制IL6和诱导IL10。此外,我们提供证据表明脂联素的一些抗炎作用部分是通过抑制NFκB信号传导和ERK1/2活性介导的。

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