Raben D M, Cunningham D D
J Cell Physiol. 1985 Dec;125(3):582-90. doi: 10.1002/jcp.1041250330.
The effects of growth factors on inositol-containing phospholipids were investigated to test the hypothesis that alterations in their metabolism are involved in mitogenic stimulation. Thrombin and EGF stimulated comparable increases in the synthesis (30-50%) and degradation (20-40%) of phosphatidylinositol 4-monophosphate (DPI) and phosphatidylinositol 4,5-bisphosphate (TPI) in a cell line which is mitogenically responsive to both growth factors. The increases in synthesis were time and dose dependent in a manner which was consistent with their involvement in mitogenesis; the increases were observed only under conditions where a mitogenic response occurred. While it has been suggested that an increased synthesis of phosphatidylinositol (PI) is coupled to the stimulation of DPI and TPI synthesis, we found that thrombin stimulated an early synthesis PI but EGF did not. To further evaluate the involvement of PI in thrombin-stimulated cell division we determined the time and dose dependence of the stimulated PI synthesis and found that it also occurred in a manner which was consistent with its involvement in thrombin-stimulated cell division. Furthermore, the stimulated PI synthesis was not observed with nonmitogenic proteases or in cell lines which were not responsive to thrombin. These results demonstrate that the metabolism of DPI and TPI appears closely related to the mitogenic response generated by EGF and thrombin. However, an early stimulation of PI synthesis is not coupled to this metabolism and is not necessary for mitogenic stimulation by EGF. Thus, a stimulation of PI synthesis is not a valid measure of alterations in inositol-containing phospholipids and what has been termed the "PI response."
研究了生长因子对含肌醇磷脂的影响,以检验其代谢改变参与有丝分裂刺激这一假说。凝血酶和表皮生长因子(EGF)在一个对两种生长因子均有丝裂原反应的细胞系中,刺激磷脂酰肌醇4-单磷酸(DPI)和磷脂酰肌醇4,5-二磷酸(TPI)的合成(增加30 - 50%)和降解(增加20 - 40%)达到相当的程度。合成的增加具有时间和剂量依赖性,其方式与它们参与有丝分裂生成一致;仅在发生有丝分裂反应的条件下观察到增加。虽然有人提出磷脂酰肌醇(PI)合成增加与DPI和TPI合成的刺激相关联,但我们发现凝血酶刺激PI早期合成,而EGF则不然。为了进一步评估PI在凝血酶刺激的细胞分裂中的作用,我们确定了刺激的PI合成的时间和剂量依赖性,发现其发生方式也与它参与凝血酶刺激的细胞分裂一致。此外,用无丝裂原活性的蛋白酶或对凝血酶无反应的细胞系未观察到刺激的PI合成。这些结果表明,DPI和TPI的代谢似乎与EGF和凝血酶产生的有丝分裂反应密切相关。然而,PI合成的早期刺激与这种代谢无关,且对于EGF的有丝分裂刺激不是必需的。因此,PI合成的刺激不是含肌醇磷脂改变及所谓“PI反应”的有效衡量指标。