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首页> 外文期刊>Biochemistry and Cell Biology >Chronic activation of pattern recognition receptors suppresses brown adipogenesis of multipotent mesodermal stem cells and brown pre-adipocytes
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Chronic activation of pattern recognition receptors suppresses brown adipogenesis of multipotent mesodermal stem cells and brown pre-adipocytes

机译:模式识别受体的慢性激活抑制了多能中胚层干细胞和棕色前脂肪细胞的棕色脂肪生成

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Brown adipose tissue (BAT) holds promise to combat obesity through energy-spending, non-shivering thermogenesis. Understanding of regulation of BAT development can lead to novel strategies to increase BAT mass and function for obesity treatment and prevention. Here, we report the effects of chronic activation of PRR on brown adipogenesis of multipotent mesodermal stem C3H10T1/2 cells and immortalized brown pre-adipocytes from the classical interscapular BAT of mice. Activation of NOD1, TLR4, or TLR2 by their respective synthetic ligand suppressed brown marker gene expression and lipid accumulation during differentiation of brown-like adipocytes of C3H10T1/2. Activation of the PRR only during the commitment was sufficient to suppress the differentiation. PRR activation suppressed PGC-1 alpha mRNA, but induced PRDM16 mRNA at the commitment. Consistently, PRR activation suppressed the differentiation of immortalized brown pre-adipocytes. Activation of PRR induced NF-kappa B activation in both cells, which correlated with their abilities to suppress PPAR gamma transactivation, a critical event for brown adipogenesis. Taken together, our results demonstrate that chronic PRR activation suppressed brown adipogenesis of multipotent mesodermal stem cells and brown pre-adipocytes, possibly through suppression of PPAR gamma transactivation. The results suggest that anti-inflammatory therapies targeting PRRs may be beneficial for the BAT development.
机译:棕色脂肪组织(BAT)有望通过节省能量,无颤抖的生热作用对抗肥胖症。对BAT发育规律的理解可以导致增加肥胖治疗和预防的BAT质量和功能的新策略。在这里,我们报告PRR的慢性激活对多能中胚层干C3H10T1 / 2细胞和永生化的棕色肩inter间BAT的棕色前脂肪细胞的棕色脂肪形成的影响。 NOD1,TLR4或TLR2各自的合成配体的激活抑制了C3H10T1 / 2褐色脂肪细胞分化过程中褐色标记基因的表达和脂质蓄积。仅在承诺期间激活PRR足以抑制差异。 PRR激活抑制了PGC-1αmRNA,但是在承诺时诱导了PRDM16 mRNA。一致地,PRR激活抑制了永生化的棕色前脂肪细胞的分化。 PRR的激活在两个细胞中诱导NF-κB激活,这与其抑制PPARγ反式激活的能力有关,这是棕色脂肪形成的关键事件。两者合计,我们的结果表明,慢性PRR激活可能通过抑制PPARγ反式激活来抑制多能中胚层干细胞和棕色前脂肪细胞的棕色脂肪生成。结果表明靶向PRR的抗炎疗法可能对BAT的发展有益。

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