Myrdal S E, Auersperg N
J Cell Biol. 1986 Apr;102(4):1224-9. doi: 10.1083/jcb.102.4.1224.
KNRK cells (a normal rat kidney [NRK] cell line transformed by Kirsten murine sarcoma virus) in sparse culture exhibit a highly ruffled morphology, but the cause of this ruffling is unknown. In this study, we have demonstrated that the continuous, excess ruffling on KNRK cells is caused by one or more soluble agents secreted by the KNRK cells themselves. To do this study, an assay for ruffling responses in live cell cultures was defined, and its reproducibility was demonstrated. This assay permitted observation of the kinetics of ruffling responses (percentage of cells ruffled as a function of time after stimulation). This method was used to compare the kinetics of ruffling induced by insulin, epidermal growth factor, fibroblast growth factor, glucose, and KNRK cell conditioned medium (CM). Ruffling was elicited on NRK cells by each of the polypeptide mitogens and nutrients, but, in each case, this ruffling subsided spontaneously within an hour. CM from KNRK cells also caused ruffling movements on untransformed NRK cells, but this ruffling continued for at least 20 h. This response was largely blocked by premixing the KNRK cell CM with rabbit IgG against rat transforming growth factor, type alpha, (TGF-alpha). KNRK cells made quiescent (ruffle free) by a pH shift (from 7.4 to 8.4) responded to insulin, glucose, and KNRK cell CM with kinetics similar to those observed for each of these factors in NRK cells. The unusual feature for the ruffle-inducing agent(s) produced by KNRK cells was that this activity was not subject, in either NRK or KNRK cells, to the cellular off-regulation that limits the responses to insulin or glucose. Thus, the continuous ruffling of KNRK cells is caused by their own unregulated ruffle-inducing agent or agents, which appear to include TGF-alpha. This work also demonstrates that kinetic analysis of cellular responses to exogenous factors can provide new insights into the regulatory mechanisms involved in the normal limitation of these responses.
KNRK细胞(一种由 Kirsten 鼠肉瘤病毒转化的正常大鼠肾[NRK]细胞系)在稀疏培养时呈现出高度褶皱的形态,但这种褶皱的原因尚不清楚。在本研究中,我们证明了KNRK细胞上持续的过度褶皱是由KNRK细胞自身分泌的一种或多种可溶性因子引起的。为了进行这项研究,定义了一种活细胞培养中褶皱反应的测定方法,并证明了其可重复性。该测定方法允许观察褶皱反应的动力学(刺激后褶皱细胞的百分比随时间的变化)。该方法用于比较胰岛素、表皮生长因子、成纤维细胞生长因子、葡萄糖和KNRK细胞条件培养基(CM)诱导的褶皱动力学。每种多肽有丝分裂原和营养物质都能在NRK细胞上引发褶皱,但在每种情况下,这种褶皱在一小时内会自发消退。KNRK细胞的CM也会在未转化的NRK细胞上引起褶皱运动,但这种褶皱会持续至少20小时。通过将KNRK细胞CM与抗大鼠转化生长因子α(TGF-α)的兔IgG预混合,这种反应在很大程度上被阻断。通过pH值变化(从7.4变为8.4)使KNRK细胞静止(无褶皱)后,它们对胰岛素、葡萄糖和KNRK细胞CM的反应动力学与在NRK细胞中观察到的这些因子的反应动力学相似。KNRK细胞产生的褶皱诱导剂的不寻常特征是,在NRK细胞或KNRK细胞中,这种活性不受限制对胰岛素或葡萄糖反应的细胞下调调节。因此,KNRK细胞的持续褶皱是由其自身不受调节的一种或多种褶皱诱导剂引起的,这些诱导剂似乎包括TGF-α。这项工作还表明,对细胞对外源因子反应的动力学分析可以为这些反应正常限制所涉及的调节机制提供新的见解。