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The brominated flame retardant PBDE 99 promotes adipogenesis via regulating mitotic clonal expansion and PPAR7 expression

机译:溴化阻燃PBDE 99通过调节丝分裂克隆膨胀和PPAR7表达来促进脂肪生物

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摘要

"Obesogens" have been widely accepted as chemicals that promote obesity, and there are many environmental pollutants that were functionally identified as obesogens. PBDE 99 is one of the most abundant PBDE congeners detected in human. However, its obesogenic effects are poorly understood. Here, we explore the in vitro effects of PBDE 99 on adipogenesis, which is a key process in obesogenesis. We observed an increase in adipogenesis when differentiating cells were exposed to PBDE 99. Further, the promoting effects of PBDE 99 on adipogenesis were most efficient during the first 4 days of 313-L1 differentiation. Consistent with this, early transcriptional factor CCAAT/enhancer-binding proteins beta (C/EBP beta) was upregulated at Days 1 and 2 during differentiation, which is accompanied with the acceleration of mitotic clonal expansion (MCE) and the upregulation of terminal transcriptional factors C/EBP alpha and PPAR gamma 2 from Day 2 or Day 4. Additionally, bisulfite genomic sequencing analysis revealed that PBDE 99 decreased methylation status of the CpG sites at PPAR gamma promoter region. Collectively, these findings demonstrate that PBDE 99 may be a potential environmental obesogen by promoting adipogenesis through facilitating MCE progression at early differentiation stage and upregulating key adipogenic factor PPAR gamma 2 expression both in direct transcriptional and epigenetic regulation dependent manner. (C) 2019 Elsevier B.V. All rights reserved.
机译:“Obesgens”被广泛接受为促进肥胖的化学品,并且有许多环境污染物在功能上被鉴定为萎缩。 PBDE 99是在人类中检测到的最丰富的PBDE同源物之一。然而,其萎缩的效果被理解得很差。在这里,我们探讨了PBDE 99对脂肪生成的体外影响,这是萎缩性的关键过程。当将区分细胞暴露于PBDE 99时,我们观察到脂肪生成的增加。此外,在313-L1分化的前4天期间,PBDE 99对脂肪发生的促进作用最有效。与此一致,在分化期间的第1天和第2天,在分化期间上调早期转录因子CCAAT /增强子结合蛋白β(C / EBPβ),其伴随着丝分裂克隆膨胀(MCE)的加速和终端转录因子的上调来自第2天或第4天的C / EBPα和PPARγ2.此外,Bisulfite基因组测序分析显示,PBDE 99降低了PPARγ启动子区的CPG位点的甲基化状态。总的来说,这些研究结果表明,通过在早期分化阶段促进MCE进展,通过促进伴随患者进展,在直接转录和表观遗传调节依赖性方式中促进MCE进展,PBDE 99可以是潜在的环境嗜血孔。 (c)2019 Elsevier B.v.保留所有权利。

著录项

  • 来源
    《The Science of the Total Environment》 |2019年第20期|67-77|共11页
  • 作者单位

    Chinese Acad Sci Res Ctr Ecoenvironm Sci State Key Lab Environm Chem & Ecotoxicol Beijing 100085 Peoples R China|Univ Chinese Acad Sci Beijing 100049 Peoples R China;

    Chinese Acad Sci Res Ctr Ecoenvironm Sci State Key Lab Environm Chem & Ecotoxicol Beijing 100085 Peoples R China;

    Univ Chinese Acad Sci Beijing 100049 Peoples R China;

    Chinese Acad Sci Res Ctr Ecoenvironm Sci State Key Lab Environm Chem & Ecotoxicol Beijing 100085 Peoples R China|Univ Chinese Acad Sci Beijing 100049 Peoples R China;

    Chinese Acad Sci Res Ctr Ecoenvironm Sci State Key Lab Environm Chem & Ecotoxicol Beijing 100085 Peoples R China|Univ Chinese Acad Sci Beijing 100049 Peoples R China;

    Chinese Acad Sci Res Ctr Ecoenvironm Sci State Key Lab Environm Chem & Ecotoxicol Beijing 100085 Peoples R China;

    Univ Copenhagen Fac Hlth & Med Sci Novo Nordisk Fdn Ctr Basic Metab Res Copenhagen Denmark;

    Chinese Acad Sci Res Ctr Ecoenvironm Sci State Key Lab Environm Chem & Ecotoxicol Beijing 100085 Peoples R China|Univ Chinese Acad Sci Beijing 100049 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    3T3-L1; C/EBP beta; Epigenetic modification; Obesogen;

    机译:3T3-L1;C / EBP Beta;表观遗传修饰;血对药;

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