Savas U, Christou M, Jefcoate C R
Department of Pharmacology, University of Wisconsin Medical School, Madison 53706.
Carcinogenesis. 1993 Oct;14(10):2013-8. doi: 10.1093/carcin/14.10.2013.
Stromal cells from mouse endometrium, E041 cells, at passages 21, 23 and 26 were metabolically active towards 7,12-dimethylbenz[a]anthracene (DMBA). The total DMBA-metabolizing activity of E041 cells was preferentially increased by benz[a]anthracene (BA) relative to 2,3,7,8-tetrachloro-dibenzo-p-dioxin (TCDD) treatment (7-fold by BA and 4-fold by TCDD), but the relative proportions of DMBA metabolites formed remained unchanged. Profiles of DMBA metabolites generated from E041 cell microsomes were very different from that of mouse P4501A1 but exhibited similarities to that of P450EF, the polycyclic aromatic hydrocarbon (PAH)-inducible cytochrome P450 in the mouse embryo fibroblast cell line C3H10T1/2 (10T1/2). Notably, both induced and uninduced E041 cell microsomes were very effective in the formation of the proximate carcinogen DMBA-3,4-dihydrodiol (15-20% of total) and DMBA-10,11-dihydrodiol (13-18% of total) but ineffective in forming the 7-hydroxymethyl derivative of DMBA (< 1% of total). Antibodies to P450EF completely inhibited the DMBA-metabolizing activities of both induced and uninduced E041 cell microsomes, with an effectiveness similar to that in microsomes prepared from identically treated 10T1/2 cells. Anti-P4501A1 had no inhibitory effect on DMBA metabolism by either induced or uninduced E041 cell microsomes. Total DMBA-metabolizing activities in BA- and TCDD-induced E041 cells were consistently 2-fold lower compared to those in similarly treated 10T1/2 cells. In addition, both induced and uninduced E041 cell microsomes formed a lower proportion of DMBA dihydrodiols relative to phenols in comparison to identically treated 10T1/2 cell microsomes (0.5 versus 1). Addition of exogenous epoxide hydrolase to E041 cell microsomes resulted in a product distribution indistinguishable from that in 10T1/2 cells. Immunoblots demonstrated 5-fold lower levels of epoxide hydrolase in E041 cell microsomes compared to 10T1/2 cell microsomes. Anti-P450EF immunoblotted a 55 kd protein in E041 cell microsomes that was induced 14-fold by BA and 6-fold by TCDD, thus paralleling the increases in the respective DMBA metabolism. It is therefore concluded that following PAH exposure endometrial stromal cells express the novel PAH-inducible mouse embryo fibroblast P450 and fail to express P4501A1.
来自小鼠子宫内膜的基质细胞E041,传代至第21、23和26代时,对7,12-二甲基苯并[a]蒽(DMBA)具有代谢活性。相对于2,3,7,8-四氯二苯并对二恶英(TCDD)处理,苯并[a]蒽(BA)优先增加E041细胞的总DMBA代谢活性(BA增加7倍,TCDD增加4倍),但形成的DMBA代谢物的相对比例保持不变。E041细胞微粒体产生的DMBA代谢物谱与小鼠P4501A1的谱非常不同,但与P450EF的谱相似,P450EF是小鼠胚胎成纤维细胞系C3H10T1/2(10T1/2)中多环芳烃(PAH)诱导的细胞色素P450。值得注意的是,诱导和未诱导的E041细胞微粒体在形成近端致癌物DMBA-3,4-二氢二醇(占总量的15-20%)和DMBA-10,11-二氢二醇(占总量的13-18%)方面非常有效,但在形成DMBA的7-羟甲基衍生物方面无效(占总量的<1%)。针对P450EF的抗体完全抑制了诱导和未诱导的E041细胞微粒体的DMBA代谢活性,其有效性与从相同处理的10T1/2细胞制备的微粒体相似。抗P4501A1对诱导或未诱导的E041细胞微粒体的DMBA代谢均无抑制作用。与相同处理的10T1/2细胞相比,BA和TCDD诱导的E041细胞中的总DMBA代谢活性始终低2倍。此外,与相同处理的10T1/2细胞微粒体相比,诱导和未诱导的E041细胞微粒体形成的DMBA二氢二醇相对于酚的比例更低(0.5对1)。向E041细胞微粒体中添加外源性环氧化物水解酶导致产物分布与10T1/2细胞中的无法区分。免疫印迹显示,E041细胞微粒体中环氧化物水解酶的水平比10T1/2细胞微粒体低5倍。抗P450EF免疫印迹在E041细胞微粒体中检测到一种55 kd的蛋白质,该蛋白质在BA诱导下增加14倍,在TCDD诱导下增加6倍,因此与各自的DMBA代谢增加情况平行。因此得出结论,PAH暴露后,子宫内膜基质细胞表达新型PAH诱导的小鼠胚胎成纤维细胞P450,而不表达P4501A1。