Systemic Physiological and Ecotoxicological Research (SPHERE), Department of Biology, University of Antwerp, Groenenborgerlaan 171, 2020 Antwerpen, Belgium.
Mol Cell Endocrinol. 2013 May 6;370(1-2):52-64. doi: 10.1016/j.mce.2013.02.011. Epub 2013 Feb 18.
Obesogenic compounds are chemicals that have an influence on obesity development. This study was designed to unravel the molecular mechanisms of the model obesogen TBT, using microarray analysis in the 3T3-L1 in vitro system, and to evaluate the use of toxicogenomics for obesogen screening. The microarray results revealed enrichment of Gene Ontology terms involved in energy and fat metabolism after 10 days of TBT exposure. Pathway analysis unveiled PPAR signalling pathway as the sole pathway significantly enriched after 1 day and the most significantly enriched pathway after 10 days of exposure. To our knowledge, this is the first study delivering an in depth mechanistic outline of the mode of action of TBT as an obesogen, combining effects on both cell physiological and gene expression level. Furthermore, our results show that combining transcriptomics with 3T3-L1 cells is a promising tool for screening of potential obesogenic compounds.
致胖化合物是指对肥胖发展有影响的化学物质。本研究旨在利用 3T3-L1 体外系统中的基因芯片分析,揭示模型致胖剂 TBT 的分子机制,并评估毒理基因组学在致胖筛选中的应用。基因芯片结果显示,TBT 暴露 10 天后,与能量和脂肪代谢相关的基因本体论术语富集。通路分析揭示了 PPAR 信号通路是唯一在暴露 1 天后显著富集的通路,也是暴露 10 天后最显著富集的通路。据我们所知,这是第一项深入研究 TBT 作为致胖剂作用模式的机制概述的研究,结合了对细胞生理和基因表达水平的影响。此外,我们的研究结果表明,将转录组学与 3T3-L1 细胞相结合是筛选潜在致胖化合物的一种很有前途的工具。