Vesey D A, Cunningham J M, Selden A C, Woodman A C, Hodgson H J
Department of Medicine, Royal Postgraduate Medical School, London, U.K.
Biochem J. 1991 Aug 1;277 ( Pt 3)(Pt 3):773-7. doi: 10.1042/bj2770773.
Culture of Hep G2 cells in medium containing 2% (v/v) dimethyl sulphoxide (DMSO) resulted in a slowing of growth and a marked change in morphological appearance. By day 6, cultures containing DMSO had one-third the number of cells compared with parallel control cultures. Measurement of 125I-epidermal-growth-factor (EGF) binding to DMSO-treated cells revealed a striking time-dependent elevation in specific EGF binding to their cell surface. Increased binding was detectable within 24 h of the start of DMSO treatment, reaching, by 6 days, levels almost 25 times greater than those for control cells. Addition of EGF to DMSO-treated cells caused a rapid down-regulation of the EGF receptor, but did not alter their proliferation rate. Slowing of growth by other means, such as serum starvation, growth to confluence or culture in the presence of sodium butyrate, did not affect 125I-EGF binding, indicating a specific effect of DMSO on these cells.
在含有2%(体积/体积)二甲基亚砜(DMSO)的培养基中培养Hep G2细胞,导致细胞生长放缓且形态外观发生显著变化。到第6天,含有DMSO的培养物中的细胞数量仅为平行对照培养物的三分之一。对与DMSO处理细胞结合的125I-表皮生长因子(EGF)进行测量发现,其与细胞表面的特异性EGF结合呈现出显著的时间依赖性升高。在开始用DMSO处理后的24小时内即可检测到结合增加,到第6天,其水平几乎比对照细胞高25倍。向DMSO处理的细胞中添加EGF会导致EGF受体迅速下调,但不会改变其增殖速率。通过其他方式使生长放缓,如血清饥饿、生长至汇合状态或在丁酸钠存在的情况下培养,均不影响125I-EGF结合,这表明DMSO对这些细胞具有特异性作用。