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脂联素亚型在人单核细胞中的不同作用。

Different effects of adiponectin isoforms in human monocytic cells.

作者信息

Neumeier Markus, Weigert Johanna, Schäffler Andreas, Wehrwein Gabriele, Müller-Ladner Ulf, Schölmerich Jürgen, Wrede Christian, Buechler Christa

机构信息

Department of Internal Medicine I, University of Regensburg, D-93042 Regensburg, Germany.

出版信息

J Leukoc Biol. 2006 Apr;79(4):803-8. doi: 10.1189/jlb.0905521. Epub 2006 Jan 24.

DOI:10.1189/jlb.0905521
PMID:16434692
Abstract

Adiponectin (APM) is an adipocyte-derived adipokine with immunosuppressive, antidiabetic, and antiatherosclerotic properties. Low molecular weight (LMW)- and higher molecular weight (HMW)-APM circulate in the serum and activate different signaling pathways. We were interested to see whether LMW-APM exerts different effects on monocytic cells compared with the HMW isoform. Therefore, the effects of recombinant LMW-APM produced in insect cells and the APM from higher eukaryotic cells containing HMW forms on monocytic cells were investigated with respect to apoptosis and inflammation. LMW- and HMW-APM induce apoptosis in nondifferentiated THP-1 cells, reduce macrophage scavenger receptor (MSR) A mRNA expression, and stimulate phosphorylation of adenosine monophosphate-activated protein kinase (AMPK). However, HMW-APM induces the secretion of interleukin (IL)-6 in human monocytes and THP-1 cells but does not suppress lipopolysaccharide (LPS)-induced IL-6 secretion. In contrast, LMW-APM reduces LPS-mediated IL-6 release and furthermore, stimulates IL-10 secretion, most likely by reducing the abundance of inhibitor of nuclear factor (NF)-kappaB kinase beta, leading to a diminished nuclear translocation of NF-kappaB p65. Our data indicate that the different APM isoforms do share common effects on monocytic cells but also induce isoform-specific responses. Although apoptosis, the activation of AMPK, and the reduction of MSR are mediated by all APM isoforms, only LMW-APM displays anti-inflammatory properties.

摘要

脂联素(APM)是一种由脂肪细胞分泌的脂肪因子,具有免疫抑制、抗糖尿病和抗动脉粥样硬化特性。低分子量(LMW)和高分子量(HMW)的APM在血清中循环并激活不同的信号通路。我们想了解LMW-APM与HMW亚型相比,对单核细胞是否有不同作用。因此,研究了昆虫细胞中产生的重组LMW-APM以及含有HMW形式的高等真核细胞来源的APM对单核细胞凋亡和炎症的影响。LMW-APM和HMW-APM均可诱导未分化的THP-1细胞凋亡,降低巨噬细胞清道夫受体(MSR)A的mRNA表达,并刺激腺苷酸活化蛋白激酶(AMPK)的磷酸化。然而,HMW-APM可诱导人单核细胞和THP-1细胞分泌白细胞介素(IL)-6,但不能抑制脂多糖(LPS)诱导的IL-6分泌。相反,LMW-APM可减少LPS介导的IL-6释放,此外,还刺激IL-10分泌,这很可能是通过降低核因子(NF)-κB激酶β抑制剂的丰度,导致NF-κB p65的核转位减少。我们的数据表明,不同的APM亚型对单核细胞有共同作用,但也会诱导亚型特异性反应。虽然所有APM亚型均可介导细胞凋亡、AMPK激活和MSR降低,但只有LMW-APM具有抗炎特性。

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