Yin Lei, Yu Kevin Shengyang, Lu Kun, Yu Xiaozhong
Department of Environmental Health Science, University of Georgia, Athens, GA, United States.
Department of Environmental Health Science, University of Georgia, Athens, GA, United States.
Toxicol In Vitro. 2016 Apr;32:297-309. doi: 10.1016/j.tiv.2016.01.010. Epub 2016 Jan 25.
Benzyl butyl phthalate (BBP) has been known to induce developmental and reproductive toxicity. However, its association with dysregulation of adipogenesis has been poorly investigated. The present study aimed to examine the effect of BBP on the adipogenesis, and to elucidate the underlying mechanisms using the 3T3-L1 cells. The capacity of BBP to promote adipogenesis was evaluated by multiple staining approaches combined with a High Content Cellomics analysis. The dynamic changes of adipogenic regulatory genes and proteins were examined, and the metabolite profile was identified using GC/MC based metabolomic analysis. The High Content analysis showed BBP in contrast with Bisphenol A (BPA), a known environmental obesogen, increased lipid droplet accumulation in a similar dose-dependent manner. However, the size of the lipid droplets in BBP-treated cells was significantly larger than those in cells treated with BPA. BBP significantly induced mRNA expression of transcriptional factors C/EBPα and PPARγ, their downstream genes, and numerous adipogenic proteins in a dose and time-dependent manner. Furthermore, GC/MC metabolomic analysis revealed that BBP exposure perturbed the metabolic profiles that are associated with glyceroneogenesis and fatty acid synthesis. Altogether, our current study clearly demonstrates that BBP promoted the differentiation of 3T3-L1 through the activation of the adipogenic pathway and metabolic disturbance.
邻苯二甲酸苄基丁酯(BBP)已知会诱发发育毒性和生殖毒性。然而,其与脂肪生成失调的关联尚未得到充分研究。本研究旨在检测BBP对脂肪生成的影响,并使用3T3-L1细胞阐明其潜在机制。通过多种染色方法结合高内涵细胞组学分析评估BBP促进脂肪生成的能力。检测脂肪生成调节基因和蛋白质的动态变化,并使用基于气相色谱/质谱联用的代谢组学分析鉴定代谢物谱。高内涵分析表明,与已知的环境致肥胖物双酚A(BPA)相比,BBP以类似的剂量依赖性方式增加脂滴积累。然而,BBP处理细胞中的脂滴大小明显大于BPA处理细胞中的脂滴。BBP以剂量和时间依赖性方式显著诱导转录因子C/EBPα和PPARγ、其下游基因以及多种脂肪生成蛋白的mRNA表达。此外,气相色谱/质谱联用代谢组学分析表明,暴露于BBP会扰乱与甘油生成和脂肪酸合成相关的代谢谱。总之,我们目前的研究清楚地表明,BBP通过激活脂肪生成途径和代谢紊乱促进3T3-L1细胞的分化。