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Maraviroc reduces cytokine expression and secretion in human adipose cells without altering adipogenic differentiation

机译:Maraviroc降低人脂肪细胞中细胞因子的表达和分泌,而不会改变脂肪形成的分化

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Maraviroc (MVC) is a drug approved for use as part of HAART in treatment-experienced HIV-1 patients with CCR5-tropic virus. Despite the current concerns on the alterations in adipose tissue that frequently appear in HIV-infected patients under HAART, there is no information available on the effects of MVC on adipose tissue. Here we studied the effects of MVC during and after the differentiation of human adipocytes in culture, and compared the results with the effects of efavirenz (EFV). We measured the acquisition of adipocyte morphology; the gene expression levels of markers for mitochondrial toxicity, adipogenesis and inflammation; and the release of adipokines and cytokines to the medium. Additionally, we determined the effects of MVC on lipopolysaccharide (LPS)-induced pro-inflammatory cytokine expression in adipocytes. Unlike EFV-treated pre-adipocytes, MVC-treated pre-adipocytes showed no alterations in the capacity to differentiate into adipocytes and accumulated lipids normally. Consistent with this, there were no changes in the mRNA levels of PPAR?? or SREBP-1c, two master regulators of adipogenesis. In addition, MVC caused a significant decrease in the gene expression and release of pro-inflammatory cytokines, whereas EFV had the opposite effect. Moreover, MVC lowered inflammation-related gene expression and inhibited the LPS-induced expression of pro-inflammatory genes in differentiated adipocytes. We conclude that MVC does not alter adipocyte differentiation but rather shows anti-inflammatory properties by inhibiting the expression and secretion of pro-inflammatory cytokines. Collectively, our results suggest that MVC may minimize adverse effects on adipose tissue development, metabolism, and inflammation, and thus could be a potentially beneficial component of antiretroviral therapy. ? 2013 Elsevier Ltd.
机译:Maraviroc(MVC)是一种经批准可作为HAART的药物,用于治疗经验丰富的CCR5-tropic病毒的HIV-1患者。尽管目前对在HAART下感染HIV的患者中经常出现的脂肪组织变化存在担忧,但尚无关于MVC对脂肪组织影响的信息。在这里,我们研究了培养中人脂肪细胞分化过程中和分化后MVC的作用,并将结果与​​依非韦伦(efavirenz,EFV)的作用进行了比较。我们测量了脂肪细胞形态的获得;线粒体毒性,脂肪形成和炎症标志物的基因表达水平;以及脂肪因子和细胞因子向培养基的释放。此外,我们确定了MVC对脂多糖(LPS)诱导的脂肪细胞促炎细胞因子表达的影响。与EFV处理的前脂肪细胞不同,MVC处理的前脂肪细胞在分化为脂肪细胞和正常积累脂质的能力上没有任何变化。与此相一致,PPARα2的mRNA水平没有变化。或SREBP-1c,这两个主要的脂肪形成调节剂。此外,MVC导致促炎细胞因子的基因表达和释放显着下降,而EFV则相反。此外,MVC降低了炎症相关基因的表达,并抑制了LPS诱导的分化脂肪细胞中促炎基因的表达。我们得出的结论是,MVC不会改变脂肪细胞的分化,而是通过抑制促炎性细胞因子的表达和分泌来显示抗炎特性。总的来说,我们的结果表明,MVC可以最大程度地减少对脂肪组织发育,代谢和炎症的不利影响,因此可能是抗逆转录病毒疗法的潜在有益成分。 ? 2013爱思唯尔有限公司

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