Department of Toxicology, School of Public Health, Beijing Key Laboratory of Toxicological Research and Risk Assessment for Food Safety, Peking University, Beijing, China.
J Appl Toxicol. 2022 Apr;42(4):588-599. doi: 10.1002/jat.4241. Epub 2021 Sep 22.
Obesogens are a subset of endocrine disruptor chemicals (EDCs) that cause obesity. The typical EDC 4-nonylphenol (4-NP) has been identified as an obesogen. However, the in vitro effects of 4-NP on adipogenesis remain unclear. In this study, 3T3-L1 preadipocytes and C3H/10T1/2 mesenchymal stem cells (MSCs) were used to investigate the influence of 4-NP on adipogenesis. The differentiation protocols for 3T3-L1 preadipocytes and C3H/10T1/2 MSCs took 8 and 12 days, respectively, beginning at Day 0. In differentiated 3T3-L1 preadipocytes, 20 μM 4-NP decreased cell viability on Days 4 and 8. Exposure to 4-NP inhibited triglyceride (TG) accumulation and adipogenic marker expression on Days 0-8, but the inhibitory effects were weaker on Days 2-8. The protein expression of pSTAT3 or STAT3 decreased on Days 0-8 and 2-8. Conversely, 4-NP promoted TG accumulation and the adipogenic marker expression in C3H/10T1/2 adipocytes. The opposing effects were attributed to physiological differences between the two cell lines. The 3T3-L1 preadipocytes are dependent on mitotic clonal expansion (MCE) to drive differentiation, while C3H/10T1/2MSCs and human preadipocytes are not. Additionally, 4-NP downregulated β-catenin expression in C3H/10T1/2 adipocytes. Accordingly, we hypothesized that 4-NP promotes adipogenesis. The role of the canonical Wnt pathway in the promotion of adipogenesis by 4-NP requires further validation. This study provides new insights into the mechanisms and appropriate risk management of 4-NP.
肥胖物是内分泌干扰物(EDCs)的一个亚类,可导致肥胖。典型的 EDC 4-壬基酚(4-NP)已被确定为肥胖物。然而,4-NP 对脂肪生成的体外影响尚不清楚。在这项研究中,使用 3T3-L1 前脂肪细胞和 C3H/10T1/2 间充质干细胞(MSCs)来研究 4-NP 对脂肪生成的影响。3T3-L1 前脂肪细胞和 C3H/10T1/2 MSC 的分化方案分别从第 0 天开始需要 8 天和 12 天。在分化的 3T3-L1 前脂肪细胞中,20μM 4-NP 在第 4 天和第 8 天降低细胞活力。暴露于 4-NP 抑制第 0-8 天和第 2-8 天的甘油三酯(TG)积累和脂肪生成标志物表达,但在第 2-8 天的抑制作用较弱。第 0-8 天和第 2-8 天,pSTAT3 或 STAT3 的蛋白表达减少。相反,4-NP 促进 C3H/10T1/2 脂肪细胞中的 TG 积累和脂肪生成标志物表达。相反的作用归因于两种细胞系之间的生理差异。3T3-L1 前脂肪细胞依赖有丝分裂克隆扩张(MCE)来驱动分化,而 C3H/10T1/2 MSC 和人前脂肪细胞则不是。此外,4-NP 下调了 C3H/10T1/2 脂肪细胞中的β-连环蛋白表达。因此,我们假设 4-NP 促进脂肪生成。4-NP 促进脂肪生成的经典 Wnt 途径的作用需要进一步验证。本研究为 4-NP 的作用机制和适当的风险管理提供了新的见解。