Yu W, Sanders B G, Kline K
Genetics Institute, University of Texas, Austin 78712, USA.
Nutr Cancer. 1996;25(2):137-49. doi: 10.1080/01635589609514436.
RRR-alpha-tocopheryl succinate (VES) was studied for effects on murine EL-4 cell proliferation and production of interleukin-2 (IL-2) and transforming growth factor-beta (TGF-beta). VES was biphasic in its actions: 0.1 microgram/ml enhanced EL-4 cell proliferation, whereas 10-20 microgram/ml inhibited cellular proliferation. Cell-conditioned media (CM) from EL-4 cells treated with 0.2 ng/ml phorbol myristate acetate (PMA) + 0.1 microgram/ml VES contained increased amounts of IL-2, as determined by the murine cytotoxic T cell IL-2-dependent CTLL-2 bioassay. VES at 0.1 microgram/ml or 0.1 microgram/ml VES + 0.2 ng/ml PMA induced the expression of IL-2 mRNA by EL-4 cells three to nine hours after treatment. CM from EL-4 cells treated with VES at 10-20 microgram/ml exhibited potent antiproliferative activity when tested in the TGF-beta-responsive mink lung cell (Mv1Lu) bioassay and showed reduced inhibitory effects when tested on TGF-beta receptor-negative mink lung (DRA-27) cells. CM from control-treated EL-4 cells exhibited no antiproliferative activity. The VES-induced antiproliferative activity was characterized as TGF-beta by neutralization analyses and immunoprecipitation of metabolically labeled proteins with TGF-beta-specific reagents. VES treatment of EL-4 cells had no effect on TGF-beta 1 mRNA expression while downregulating TGF-beta 3 mRNA expression. In summary, these studies showed that 0.1 microgram/ml VES enhanced cellular proliferation, in part, via increased IL-2 production, whereas 10-20 micrograms/ml VES inhibited cellular proliferation, in part, via the secretion of biologically active TGF-beta.
研究了RRR-α-生育酚琥珀酸酯(VES)对小鼠EL-4细胞增殖以及白细胞介素-2(IL-2)和转化生长因子-β(TGF-β)产生的影响。VES的作用具有双相性:0.1微克/毫升可增强EL-4细胞增殖,而10 - 20微克/毫升则抑制细胞增殖。用0.2纳克/毫升佛波酯肉豆蔻酸酯(PMA)+ 0.1微克/毫升VES处理的EL-4细胞的细胞条件培养基(CM)中,通过小鼠细胞毒性T细胞IL-2依赖的CTLL-2生物测定法测定,IL-2含量增加。0.1微克/毫升的VES或0.1微克/毫升VES + 0.2纳克/毫升PMA在处理后三至九小时诱导EL-4细胞表达IL-2 mRNA。当在TGF-β反应性貂肺细胞(Mv1Lu)生物测定中测试时,用10 - 20微克/毫升VES处理的EL-4细胞的CM表现出强大的抗增殖活性,而在TGF-β受体阴性的貂肺(DRA-27)细胞上测试时,抑制作用减弱。对照处理的EL-4细胞的CM没有抗增殖活性。通过中和分析和用TGF-β特异性试剂对代谢标记蛋白进行免疫沉淀,将VES诱导的抗增殖活性鉴定为TGF-β。VES处理EL-4细胞对TGF-β1 mRNA表达没有影响,同时下调TGF-β3 mRNA表达。总之,这些研究表明,0.1微克/毫升的VES部分通过增加IL-2的产生来增强细胞增殖,而10 - 20微克/毫升的VES部分通过分泌生物活性TGF-β来抑制细胞增殖。