首页> 美国卫生研究院文献>International Journal of Molecular Sciences >In Vitro Cocktail Effects of PCB-DL (PCB118) and Bulky PCB (PCB153) with BaP on Adipogenesis and on Expression of Genes Involved in the Establishment of a Pro-Inflammatory State
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In Vitro Cocktail Effects of PCB-DL (PCB118) and Bulky PCB (PCB153) with BaP on Adipogenesis and on Expression of Genes Involved in the Establishment of a Pro-Inflammatory State

机译:含BaP的PCB-DL(PCB118)和大块PCB(PCB153)对脂肪形成和涉及促炎状态建立的基因表达的体外鸡尾酒效应

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摘要

(1) Objective: Highlight the in vitro effects of 3T3-L1 cell exposure to polychlorinated biphenyls (PCB118 and 153) or benzo(a)pyrene (BaP) alone or as a cocktail on adipogenesis (ADG) by focusing on changes in lipid metabolism and inflammatory-related genes expression (INFG) and ADG-related genes expression (ADGG); (2) Results: Treatment from the early stage of cell differentiation by BaP alone or in combination with PCBs decreased the expression of some of the ADGG (PPARγ Glut-4, FAS, Lipin-1a, Leptin, and Adiponectin). BaP enhanced the INFG, especially MCP-1 and TNFα. Co-exposure to BaP and PCB153 showed a synergistic effect on TNFα and IL6 expression. Treatment with BaP and PCBs during only the maturation period up-regulated the INFG (IL6, TNFα, CXCL-10 & MCP-1). PCB118 alone also enhanced TNFα, CXCL-10, and PAI-1 expression. The change in MCP-1 protein expression was in agreement with that of the gene. Finally, the BaP-induced up-regulation of the xenobiotic responsive element (XRE)-controlled luciferase activity was impaired by PCB153 but not by PCB118; (3) Conclusion: BaP and PCBs down-regulate a part of ADGG and enhance INFG. The direct regulatory effect of PCBs on both ADGG and INFG is usually rather lower than that of BaP and synergistic or antagonistic cocktail effects are clearly observed.
机译:(1)目的:通过集中研究脂质代谢的变化,突出3T3-L1细胞暴露于多氯联苯(PCB118和153)或苯并(a)re(BaP)或作为鸡尾酒对成脂(ADG)的体外作用炎性相关基因表达(INFG)和ADG相关基因表达(ADGG); (2)结果:从细胞分化的早期开始,单独使用BaP或与PCBs联合使用可降低某些ADGG(PPARγGlut-4,FAS,Lipin-1a,Leptin和Adiponectin)的表达。 BaP增强INFG,尤其是MCP-1和TNFα。对BaP和PCB153的共同暴露显示出对TNFα和IL6表达的协同作用。仅在成熟期使用BaP和PCB进行处理会上调INFG(IL6,TNFα,CXCL-10和MCP-1)。单独使用PCB118还可增强TNFα,CXCL-10和PAI-1的表达。 MCP-1蛋白表达的变化与该基因的变化一致。最后,PCB153而不是PCB118削弱了BaP诱导的异种反应元件(XRE)控制的荧光素酶活性的上调; (3)结论:BaP和PCB下调ADGG的一部分并增强INFG。多氯联苯对ADGG和INFG的直接调节作用通常要比BaP低得多,并且可以清楚地观察到协同或拮抗的鸡尾酒作用。

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