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甲状腺受体拮抗作用作为环境混合物在 3T3-L1 细胞中诱导脂肪生成的促成机制。

Thyroid receptor antagonism as a contributory mechanism for adipogenesis induced by environmental mixtures in 3T3-L1 cells.

机构信息

Nicholas School of the Environment, Duke University, Durham, NC 27708, United States of America.

Department of Surgery, University of California at San Francisco, San Francisco, CA, United States.

出版信息

Sci Total Environ. 2019 May 20;666:431-444. doi: 10.1016/j.scitotenv.2019.02.273. Epub 2019 Feb 18.

Abstract

We previously demonstrated that indoor house dust extracts could induce adipogenesis in pre-adipocytes, suggesting a potential role for indoor contaminant mixtures in metabolic health. Herein, we investigated the potential role of thyroid receptor beta (TRβ) antagonism in adipogenic effects (dust-induced triglyceride accumulation and pre-adipocyte proliferation) following exposure to environmental mixtures (indoor house dust extracts). Concentrations of specific flame retardants were measured in extracts, and metabolic health information was collected from residents (n = 137). 90% of dust extracts exhibited significant adipogenic activity, >60% via triglyceride accumulation, and >70% via pre-adipocyte proliferation. Triglyceride accumulation was positively correlated with concentrations of each of twelve flame retardants, despite most being independently inactive; this suggests a putative role for co-exposures or mixtures. We further reported a positive correlation between dust-induced triglyceride accumulation and serum thyroid stimulating hormone concentrations, negative correlations with serum free triiodothyronine and thyroxine concentrations, and a positive and significant association between dust-induced triglyceride accumulation and residents' body mass index (BMI). We hypothesized that inhibition of TR antagonism might counteract these effects, and both addition of a TR agonist and siRNA knock-down of TR resulted in decreased dust-induced triglyceride accumulation in a subset of samples, bolstering this as a contributory mechanism. These results highlight a contributory role of environmental TR antagonism as a putative factor in metabolic health, suggesting that further research should evaluate this mechanism and determine whether in vitro adipogenic activity could have utility as a biomarker for metabolic health in residents.

摘要

我们之前已经证明,室内灰尘提取物可以在脂肪前体细胞中诱导脂肪生成,这表明室内污染物混合物在代谢健康中可能具有潜在作用。在此,我们研究了甲状腺受体β(TRβ)拮抗作用在暴露于环境混合物(室内灰尘提取物)后对脂肪生成效应(灰尘诱导的甘油三酯积累和脂肪前体细胞增殖)的潜在作用。测量了提取物中特定阻燃剂的浓度,并从居民(n=137)处收集了代谢健康信息。90%的灰尘提取物表现出显著的脂肪生成活性,超过 60%通过甘油三酯积累,超过 70%通过脂肪前体细胞增殖。尽管大多数阻燃剂单独不活跃,但甘油三酯积累与十二种阻燃剂中的每一种的浓度呈正相关,这表明可能存在共同暴露或混合物的作用。我们进一步报告了灰尘诱导的甘油三酯积累与血清促甲状腺激素浓度呈正相关,与血清游离三碘甲状腺原氨酸和甲状腺素浓度呈负相关,与居民体重指数(BMI)呈正相关且显著相关。我们假设 TR 拮抗作用的抑制可能会抵消这些影响,TR 激动剂的添加和 TR 的 siRNA 敲低都导致了一部分样本中灰尘诱导的甘油三酯积累减少,这支持了这是一种促成机制。这些结果强调了环境 TR 拮抗作用作为代谢健康潜在因素的促成作用,表明应进一步研究该机制,并确定体外脂肪生成活性是否可作为居民代谢健康的生物标志物。

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