Whithead R H, Nice E C, Lloyd C J, James R, Burgess A W
Ludwig Institute for Cancer Research, Melbourne Tumor Biology Branch, Victoria, Australia.
Int J Cancer. 1990 Nov 15;46(5):858-63. doi: 10.1002/ijc.2910460518.
Although the colonic mucosa is one of the most rapidly proliferating epithelial tissues in the body, little is known about the factors that direct this proliferation. In this report we have studied the parameters of both a mitogenic and a clonogenic assay for detecting potential colonic growth factors (CGF). Using a colon carcinoma cell line (LIM1215), which has retained a number of the properties of normal colonic mucosa, we have assayed a range of mitogenic factors for CGF activity. 3H-thymidine incorporation by the LIM1215 cell line was stimulated by low concentrations of epidermal growth factor and basic fibroblast growth factor and, to a lesser extent, by higher concentrations of interleukin-1 and insulin-like growth factor 1. The cells did not respond to a range of other mitogens and lymphokines. Optimal clonogenic response in a soft-agar assay was obtained using a primary pituitary extract.
尽管结肠黏膜是人体中增殖最迅速的上皮组织之一,但对于指导这种增殖的因素却知之甚少。在本报告中,我们研究了用于检测潜在结肠生长因子(CGF)的促有丝分裂和克隆形成试验的参数。使用保留了许多正常结肠黏膜特性的结肠癌细胞系(LIM1215),我们检测了一系列促有丝分裂因子的CGF活性。低浓度的表皮生长因子和碱性成纤维细胞生长因子可刺激LIM1215细胞系掺入3H-胸腺嘧啶核苷,较高浓度的白细胞介素-1和胰岛素样生长因子1在较小程度上也有刺激作用。这些细胞对一系列其他促有丝分裂原和淋巴因子无反应。使用垂体提取物在软琼脂试验中获得了最佳克隆形成反应。