Curran Colleen S, Carrillo Esteban R, Ponik Suzanne M, Keely Patricia J
Department of Cell and Regenerative Biology, University of Wisconsin at Madison, Madison, WI 53706, USA.
Environ Toxicol Pharmacol. 2015 Jan;39(1):114-24. doi: 10.1016/j.etap.2014.10.017. Epub 2014 Nov 1.
Breast density, where collagen I is the dominant component, is a significant breast cancer risk factor. Cell surface integrins interact with collagen, activate focal adhesion kinase (FAK), and downstream cell signals associated with xenobiotics (AhR, ARNT) and hypoxia (HIF-1α, ARNT). We examined if mammary cells cultured in high density (HD) or low density (LD) collagen gels affected xenobiotic or hypoxic responses. ARNT production was significantly reduced by HD culture and in response to a FAK inhibitor. Consistent with a decrease in ARNT, AhR and HIF-1α reporter activation and VEGF production was lower in HD compared to LD. However, P450 production was enhanced in HD and induced by AhR and HIF-1α agonists, possibly in response to increased NF-κB activaton. Thus, collagen density differentially regulates downstream cell signals of AhR and HIF-1α by modulating the activity of FAK, the release of NF-κB transcriptional factors, and the levels of ARNT.
乳腺密度以I型胶原蛋白为主要成分,是乳腺癌的一个重要风险因素。细胞表面整合素与胶原蛋白相互作用,激活粘着斑激酶(FAK)以及与外源性物质(芳烃受体、芳烃核转运蛋白)和缺氧(缺氧诱导因子-1α、芳烃核转运蛋白)相关的下游细胞信号。我们研究了在高密度(HD)或低密度(LD)胶原蛋白凝胶中培养的乳腺细胞是否会影响外源性物质或缺氧反应。高密度培养以及使用FAK抑制剂后,芳烃核转运蛋白的产生显著减少。与芳烃核转运蛋白的减少一致,与低密度相比,高密度培养时芳烃受体和缺氧诱导因子-1α报告基因的激活以及血管内皮生长因子的产生较低。然而,高密度培养时细胞色素P450的产生增加,并由芳烃受体和缺氧诱导因子-1α激动剂诱导,这可能是对核因子κB激活增加的反应。因此,胶原蛋白密度通过调节粘着斑激酶的活性、核因子κB转录因子的释放以及芳烃核转运蛋白的水平,差异性地调节芳烃受体和缺氧诱导因子-1α的下游细胞信号。