Hayashi Y, Hirai S, Harayama H, Saito T, Ichikawa A
Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Japan.
Jpn J Pharmacol. 1990 May;53(1):1-9. doi: 10.1254/jjp.53.1.
The rate of proliferation of porcine aortic endothelial cells (PAEC) in response to fibroblast growth factor (FGF) was largely retarded when incubated in Dulbecco's modified Eagle's medium (DMEM) supplemented with either 1% fetal bovine serum (FBS) or 10% dialyzed FBS in place of 10% FBS. Proliferation of endothelial cells in low serum media in response to FGF was enhanced to the level of media containing FGF plus 10% FBS by the addition of the dialyzable fraction from bovine brain homogenates. From the bovine brain dialyzable fraction, two active components were purified and identified as hypoxanthine and inosine. Either hypoxanthine or inosine, at a dose of 5 microM in DMEM with 1% FBS, maximally increased the incorporation of [3H]thymidine into DNA of PAEC in low serum media in the presence of FGF. However, no additive effect was observed when hypoxanthine and inosine were added simultaneously. The present data indicate that the proliferative action of FGF on PAEC can be potentiated by hypoxanthine and inosine.
当猪主动脉内皮细胞(PAEC)在补充有1%胎牛血清(FBS)或10%透析FBS以替代10% FBS的杜氏改良伊格尔培养基(DMEM)中培养时,其对成纤维细胞生长因子(FGF)的增殖速率在很大程度上受到抑制。通过添加来自牛脑匀浆的可透析部分,低血清培养基中内皮细胞对FGF的增殖增强至含有FGF加10% FBS的培养基水平。从牛脑可透析部分中,纯化并鉴定出两种活性成分,即次黄嘌呤和肌苷。在含有1% FBS的DMEM中,次黄嘌呤或肌苷以5 microM的剂量,在FGF存在的情况下,最大程度地增加了低血清培养基中[3H]胸腺嘧啶核苷掺入PAEC的DNA中。然而,当同时添加次黄嘌呤和肌苷时,未观察到相加效应。目前的数据表明,次黄嘌呤和肌苷可增强FGF对PAEC的增殖作用。