Linnainmaa K, Pelin K, Vanhala E, Tuomi T, Piccoli C, Fitzgerald D J, Yamasaki H
Institute of Occupational Health, Department of Industrial Hygiene, Helsinki, Finland.
Carcinogenesis. 1993 Aug;14(8):1597-602. doi: 10.1093/carcin/14.8.1597.
We examined gap junctional intercellular communication (GJIC) of primary human mesothelial cells and cell lines of asbestos-associated human pleural mesotheliomas, and the effect of asbestos and other mineral fibres on these cells. In homologous cultures, the GJIC capacity of six out of seven tumour cell lines was markedly less than for primary mesothelial cells. This defect in GJIC appeared not to be at the expression level of mRNA and protein of the gene encoding the 43 kDa gap junction protein. In heterologous cocultures of tumour cells and primary mesothelial cells, however, 80-90% of the tumour cell/normal cell contacts were functional. Exposure of primary mesothelial cells to TPA, a phorbol ester tumour promoter, resulted in marked inhibition of GJIC, being an action common to numerous tumour promoters. Such an effect though was not observed with the carcinogenic mesothelioma-inducing mineral fibres chrysotile and amosite, neither with glass wool. These results suggest that a permanent defect in GJIC capacity is a common feature of human mesothelioma cells, but how mineral fibres are involved in the process of mesotheliomagenesis is still unclear.
我们检测了原代人间皮细胞和石棉相关的人胸膜间皮瘤细胞系的缝隙连接细胞间通讯(GJIC),以及石棉和其他矿物纤维对这些细胞的影响。在同源培养物中,七个肿瘤细胞系中有六个的GJIC能力明显低于原代间皮细胞。GJIC的这种缺陷似乎并非出现在编码43kDa缝隙连接蛋白的基因的mRNA和蛋白质表达水平上。然而,在肿瘤细胞与原代间皮细胞的异源共培养物中,80 - 90%的肿瘤细胞/正常细胞接触是有功能的。原代间皮细胞暴露于佛波酯肿瘤促进剂TPA会导致GJIC明显受到抑制,这是众多肿瘤促进剂的共同作用。然而,致癌的间皮瘤诱导矿物纤维温石棉和铁石棉以及玻璃棉均未观察到这种效应。这些结果表明,GJIC能力的永久性缺陷是人间皮瘤细胞的一个共同特征,但矿物纤维如何参与间皮瘤发生过程仍不清楚。