Mechanistical studies of the inhibition of intercellular communication by organochlorine compounds.

L Wärngárd, Y Bager, Y Kato, K Kenne, U G Ahlborg
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引用次数: 8

Abstract

Many hydrocarbons are environmental pollutants that, due to their lipophilicity and chemical stability, accumulate in biological systems including milk and body fat. A number of investigations have demonstrated that many organochlorine compounds can act as tumour promoters in vivo and inhibit gap junctional intercellular communication between cells in culture. In the present study we have investigated the dioxin 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), different polychlorinated biphenyls, chlorinated paraffins and the pesticide endosulfan. Using techniques of scrape loading dye/transfer and Western blot analysis the function, expression and phosphorylation of different connexins in vitro and in vivo were studied. The results show a good correlation between the ability to act as a tumour promoter and to interfere with gap junctional intercellular communication. All tested compounds inhibited the intercellular communication in a liver derived cell line (IAR 20). However, the results show that the time to inhibition varies between the different agents. Endosulfan and chlorinated paraffins inhibit the communication within one hour, whereas dioxin like substances need to expose the cells for 48 hours before the communication is affected.

有机氯化合物抑制细胞间通讯的机理研究。
许多碳氢化合物是环境污染物,由于它们的亲脂性和化学稳定性,在包括牛奶和身体脂肪在内的生物系统中积累。许多研究表明,许多有机氯化合物在体内可以作为肿瘤促进剂,并在培养中抑制细胞间间隙连接的细胞间通讯。本文研究了二恶英2,3,7,8-四氯二苯并对二恶英(TCDD)、不同的多氯联苯、氯化石蜡和农药硫丹。采用刮载染色/转移技术和Western blot技术研究了不同连接蛋白在体外和体内的功能、表达和磷酸化。结果表明,作为肿瘤启动子的能力与干扰间隙连接细胞间通讯之间存在良好的相关性。所有测试的化合物都抑制肝源细胞系的细胞间通讯(IAR 20)。然而,结果表明,不同的药物之间的抑制时间不同。硫丹和氯化石蜡能在一小时内抑制细胞间的通讯,而二恶英类物质则需要在细胞暴露48小时后通讯才会受到影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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