Fischer S M, Lee M L, Maldve R E, Morris R J, Trono D, Burow D L, Butler A P, Pavone A, Warren B
University of Texas M. D. Anderson Cancer Center, Science Park-Research Division, Smithville 78957.
Mol Carcinog. 1993;7(4):228-37. doi: 10.1002/mc.2940070405.
The goal of this study was to compare the response of mouse epidermal keratinocytes (MEKs) and human epidermal keratinocytes (HEKs) to 12-O-tetradecanoylphorbol-13-acetate (TPA) with respect to the activation and downregulation of protein kinase C (PKC), the expression of c-jun and c-fos, and the expression and induction of ornithine decarboxylase (ODC) activity. Keratinocytes from adult CD-1 mice and from discarded adult human skin were grown in primary culture in a high-calcium serum-free medium that supported proliferation and differentiation. Immunoblotting of freshly isolated and cultured MEKs and HEKs for isozymes of protein kinase C revealed that fresh HEKs contained PKC alpha, PKC beta, and PKC delta; no PKC gamma, PKC epsilon, or PKC zeta were detected. In fresh MEKs, PKC alpha, PKC beta, PKC delta, and PKC zeta were observed, but not PKC gamma or PKC epsilon. After 2 wk in culture, the isozyme profiles of MEKs and HEKs were similar except that PKC gamma was noticeably present in HEK cultures. Activation of partially purified total PKC by TPA was similar in freshly isolated and cultured MEKs and HEKs, indicating that the two species were similar in this regard and that 2 wk of culture did not alter this characteristic. When MEK and HEK cultures were treated with TPA for 3 h, less than 30% of the control level of PKC activity was detected, indicating that TPA-induced downregulation of PKC was similar in MEKs and HEKs. After treatment with TPA, MEK cultures produced a large induction of both c-jun and c-fos mRNA by 60 min, as determined by northern blot analysis, and a large induction of ODC mRNA and enzyme activity by 6 h. TPA treatment of cultured HEKs, however, did not induce ODC activity; in fact, less activity, compared with that of control cultures, was observed. Northern blot analysis also revealed no increase in c-jun, c-fos, and ODC mRNA in HEKs. However, c-jun and c-fos mRNA and both ODC mRNA and enzyme activity were induced in HEKs fed growth factors after several days of deprivation. This suggests that the lack of ODC induction by TPA in HEKs is probably due to species differences in downstream steps in PKC signal transduction.
本研究的目的是比较小鼠表皮角质形成细胞(MEK)和人表皮角质形成细胞(HEK)对12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)在蛋白激酶C(PKC)的激活和下调、c - jun和c - fos的表达以及鸟氨酸脱羧酶(ODC)活性的表达和诱导方面的反应。取自成年CD - 1小鼠和废弃成人皮肤的角质形成细胞在支持增殖和分化的高钙无血清培养基中进行原代培养。对新鲜分离和培养的MEK和HEK进行PKC同工酶的免疫印迹分析显示,新鲜HEK含有PKCα、PKCβ和PKCδ;未检测到PKCγ、PKCε或PKCζ。在新鲜MEK中,观察到PKCα、PKCβ、PKCδ和PKCζ,但未观察到PKCγ或PKCε。培养2周后,MEK和HEK的同工酶谱相似,只是PKCγ在HEK培养物中明显存在。TPA对部分纯化的总PKC的激活在新鲜分离和培养的MEK和HEK中相似,表明这两个物种在这方面相似,且2周的培养并未改变这一特性。当MEK和HEK培养物用TPA处理3小时后,检测到的PKC活性低于对照水平的30%,表明TPA诱导的PKC下调在MEK和HEK中相似。用TPA处理后,通过Northern印迹分析确定,MEK培养物在60分钟时c - jun和c - fos mRNA均大幅诱导,在6小时时ODC mRNA和酶活性大幅诱导。然而,TPA处理培养的HEK并未诱导ODC活性;事实上,与对照培养物相比,观察到的活性更低。Northern印迹分析还显示HEK中c - jun、c - fos和ODC mRNA没有增加。然而,在剥夺生长因子几天后再给予生长因子的HEK中,c - jun和c - fos mRNA以及ODC mRNA和酶活性均被诱导。这表明HEK中TPA未能诱导ODC可能是由于PKC信号转导下游步骤中的物种差异。