Jetten A M, Ganong B R, Vandenbark G R, Shirley J E, Bell R M
Proc Natl Acad Sci U S A. 1985 Apr;82(7):1941-5. doi: 10.1073/pnas.82.7.1941.
Tumor-promoting phorbol esters induce ornithine decarboxylase (ODCase) activity and reduce epidermal growth factor (EGF) binding in rat tracheal epithelial 2C5 cells. Phorbol esters activate protein kinase C by interacting at the same site as sn-1,2-diacylglycerols, the presumed physiological regulators. The effects of added sn-1,2-diacylglycerols and those generated by phospholipase C treatment of 2C5 cells on ODCase induction and EGF binding were investigated to establish a role for protein kinase C in these cellular responses. Treatment of 2C5 cells with phospholipase C induced ODCase activity and reduced EGF binding, whereas phospholipases A2 and D were inactive. When sn-1,2-diacylglycerols containing fatty acids 3-10 carbons in length were added to 2C5 cells, those diacylglycerols containing fatty acids 5-10 carbons in length caused ODCase induction and reduction in EGF binding. sn-1,2-Dioctanoylglycerol was one of the most active compounds tested. It induced ODCase in a dose- (50-500 microM) and time-dependent manner. The reduction of binding of 125I-labeled EGF by sn-1,2-dioctanoylglycerol was also time and dose dependent and appeared to result from a change in EGF affinity and not the number of receptor sites. This series of sn-1,2-diacylglycerols showed similar structure-function relationships in their ability to induce ODCase activity, to decrease EGF binding, to stimulate protein kinase C, and to inhibit [3H]phorbol dibutyrate binding to the phorbol ester receptor. These data demonstrate biological activities for a number of diacylglycerols and indicate that protein kinase C activation is implicated in ODCase induction and decreased EGF binding.
促肿瘤佛波酯可诱导大鼠气管上皮2C5细胞中的鸟氨酸脱羧酶(ODCase)活性,并降低表皮生长因子(EGF)的结合。佛波酯通过与假定的生理调节物sn-1,2-二酰基甘油在同一部位相互作用来激活蛋白激酶C。研究了添加的sn-1,2-二酰基甘油以及2C5细胞经磷脂酶C处理后产生的二酰基甘油对ODCase诱导和EGF结合的影响,以确定蛋白激酶C在这些细胞反应中的作用。用磷脂酶C处理2C5细胞可诱导ODCase活性并降低EGF结合,而磷脂酶A2和D则无活性。当向2C5细胞中添加含有3至10个碳原子的脂肪酸的sn-1,2-二酰基甘油时,那些含有5至10个碳原子的脂肪酸的二酰基甘油会引起ODCase诱导并降低EGF结合。sn-1,2-二辛酰甘油是测试的最具活性的化合物之一。它以剂量(50 - 500 microM)和时间依赖性方式诱导ODCase。sn-1,2-二辛酰甘油对125I标记的EGF结合的降低也是时间和剂量依赖性的,并且似乎是由EGF亲和力的变化而非受体位点数量的变化引起的。这一系列的sn-1,2-二酰基甘油在诱导ODCase活性、降低EGF结合、刺激蛋白激酶C以及抑制[3H]佛波醇二丁酸酯与佛波酯受体结合的能力方面显示出相似的结构 - 功能关系。这些数据证明了多种二酰基甘油的生物活性,并表明蛋白激酶C的激活与ODCase诱导和EGF结合减少有关。