Li Wen, Vogel Christoph F A, Matsumura Fumio
Department of Environmental Toxicology, University of California, One Shields Avenue, Davis, California 95616, USA.
J Cell Biochem. 2007 Oct 1;102(2):389-402. doi: 10.1002/jcb.21303.
Wasting syndrome is one of the hallmark symptoms of poisoning by TCDD (=dioxin), which is associated with the massive loss of adipose tissue and serum hyperlipidemia in vivo. Yet, the most widely used in vitro cell model 3T3-L1 adipocyte has not been useful for studying such an action of TCDD because of the difficulty of inducing their mature adipocytes to respond to TCDD to go through lipolysis. Here, we made efforts to find the right cell culture and treatment conditions to induce mature 3T3-L1 adipocytes to go through lipolysis, which is defined as events leading to reduction of lipids in adipocytes. The optimum condition was found to require 7-day differentiated adipocytes being subjected to DMEM medium containing TCDD (but without insulin) for 5 day incubation with two medium changes (the same composition) on incubation days 2 and 4. After 24 h, the early effect of TCDD on adipocytes was predominantly on inflammation, particularly induction of COX-2 and KC (IL-8), which is accompanied by upregulation of C/EBPbeta and delta. The sign of TCDD-induced lipolysis starts slowly and by incubation day 3, a few markers showed modestly significant changes. By day 5 of incubation, however, many markers show highly significant signs of lipolytic changes. Although this process could take place without exogenous macrophages or their cytokines, addition of exogenous TNFalpha considerably synergized this action of TCDD. In conclusion, under a right condition, 3T3-L1 adipocytes were found to respond to TCDD to go through lipolysis. The early trigger of such a response appears to be activation of COX-2, which is amplified by TNFalpha.
消瘦综合征是2,3,7,8-四氯二苯并对二恶英(=二恶英)中毒的标志性症状之一,它与体内脂肪组织的大量流失和血清高脂血症有关。然而,最广泛使用的体外细胞模型3T3-L1脂肪细胞对于研究二恶英的这种作用并无帮助,因为难以诱导其成熟脂肪细胞对二恶英作出反应并进行脂肪分解。在此,我们努力寻找合适的细胞培养和处理条件,以诱导成熟的3T3-L1脂肪细胞进行脂肪分解,脂肪分解被定义为导致脂肪细胞内脂质减少的一系列事件。发现最佳条件是让分化7天的脂肪细胞在含有二恶英(但不含胰岛素)的DMEM培养基中孵育5天,在孵育的第2天和第4天更换两次培养基(成分相同)。24小时后,二恶英对脂肪细胞的早期作用主要是引发炎症,特别是诱导COX-2和KC(白细胞介素-8),同时伴有C/EBPβ和δ的上调。二恶英诱导的脂肪分解迹象开始缓慢,到孵育第3天,一些标志物显示出适度的显著变化。然而,到孵育第5天,许多标志物显示出高度显著的脂肪分解变化迹象。尽管这个过程可以在没有外源性巨噬细胞或其细胞因子的情况下发生,但添加外源性肿瘤坏死因子α(TNFα)可显著增强二恶英的这种作用。总之,在合适的条件下,发现3T3-L1脂肪细胞对二恶英有反应并进行脂肪分解。这种反应的早期触发因素似乎是COX-2的激活,而TNFα会放大这种激活作用。