Reiners J J, Herlick S
Carcinogenesis. 1985 May;6(5):793-5. doi: 10.1093/carcin/6.5.793.
A keratinocyte cell-mediated mutation assay was used to examine the importance of cellular proximity to the transfer of mutagenic and cytotoxic polycyclic aromatic hydrocarbon (PAH) metabolites between cells. The PAHs 7,12-dimethylbenz[a]anthracene (DMBA) and benzo[a]pyrene (BP) were both mutagenic and cytotoxic to V-79 fibroblasts co-cultured on the surface of a keratinocyte feeder layer. However, neither PAH was mutagenic to the V-79 cells when the V-79 cells were co-incubated with the cultured keratinocytes under conditions in which the two cell types were separated by 0.5-1.5 mm but continually shared a common medium. Similarly, DMBA cytotoxicity was eliminated and BP-dependent cytotoxicity was greatly reduced in co-incubation protocols. These results suggest that cells must either be in contact or very close to facilitate the transfer of mutagenic PAH metabolites between cells.
采用角质形成细胞介导的突变试验,以检验细胞间接近程度对于诱变和细胞毒性多环芳烃(PAH)代谢物在细胞间转移的重要性。PAHs 7,12-二甲基苯并[a]蒽(DMBA)和苯并[a]芘(BP)对共培养于角质形成细胞饲养层表面的V-79成纤维细胞均具有诱变性和细胞毒性。然而,当V-79细胞与培养的角质形成细胞在两种细胞类型被0.5-1.5毫米分隔但持续共享共同培养基的条件下共同孵育时,两种PAHs对V-79细胞均无诱变性。同样,在共同孵育方案中,DMBA的细胞毒性消除,BP依赖性细胞毒性大幅降低。这些结果表明,细胞必须相互接触或非常接近,以促进诱变PAH代谢物在细胞间的转移。