Yamori T, Shimada K, Kanda H, Nishizuru Y, Komi A, Yamazaki K, Asanoma K, Ogawa M, Nomura K, Nemoto N, Kumada K, Tsuruo T
Division of Experimental Chemotherapy, Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo.
Jpn J Cancer Res. 1996 Feb;87(2):146-52. doi: 10.1111/j.1349-7006.1996.tb03152.x.
A hepatocyte-derived cell line designated MLE-15A2 was established from a primary culture of mouse hepatocytes. The MLE-15A2 cells appeared to retain the basic nature of hepatocytes in that they showed morphology of an epithelial cell type and secreted albumin into the culture medium. These cells were grown on collagen-coated plates and could be easily expanded to a large-scale culture. Therefore, MLE-15A2 cells may provide a more useful model for studying liver microenvironments than primary cultures of hepatocytes. We found that conditioned media from MLE-15A2 cells, as well as from primary cultures of hepatocytes, promoted the proliferation of highly liver-colonizing colon 26 NL-17 cells better than the poorly liver-colonizing colon 26 NL-4 cells. Moreover, the conditioned media stimulated the growth of some human colon cancer cell lines. These results indicate that MLE-15A2 cells secrete growth factors that selectively stimulate certain tumor cell types. Hepatocyte-derived growth factors may regulate selective survival and colonization of tumor cells in the process of liver metastasis. The growth-promoting activity was unaffected by dialysis, was stable at 80 degrees C for 30 minutes and was bound to a heparin-Sepharose column. The major activity was eluted from the column with 0.7-0.75 M NaCl, and some minor activities eluted with lower concentrations of NaCl. These results suggest that the active components are heterogeneous heparin-binding proteins with lower affinity to heparin than platelet-derived and fibroblast growth factors.
一种名为MLE-15A2的肝细胞衍生细胞系是从小鼠肝细胞原代培养物中建立的。MLE-15A2细胞似乎保留了肝细胞的基本特性,因为它们呈现上皮细胞类型的形态,并向培养基中分泌白蛋白。这些细胞在胶原包被的培养板上生长,并且可以很容易地扩大到大规模培养。因此,与肝细胞原代培养相比,MLE-15A2细胞可能为研究肝脏微环境提供更有用的模型。我们发现,来自MLE-15A2细胞以及肝细胞原代培养物的条件培养基,促进高肝脏定植的结肠26 NL-17细胞增殖的能力优于低肝脏定植的结肠26 NL-4细胞。此外,条件培养基刺激了一些人结肠癌细胞系的生长。这些结果表明,MLE-15A2细胞分泌选择性刺激某些肿瘤细胞类型的生长因子。肝细胞衍生的生长因子可能在肝转移过程中调节肿瘤细胞的选择性存活和定植。促生长活性不受透析影响,在80℃下30分钟稳定,并且与肝素-琼脂糖柱结合。主要活性用0.7 - 0.75M NaCl从柱上洗脱,一些次要活性用较低浓度的NaCl洗脱。这些结果表明,活性成分是与肝素结合的异质性蛋白质,与血小板衍生生长因子和成纤维细胞生长因子相比,它们对肝素的亲和力较低。