Eshel R, Firon M, Katz B Z, Sagi-Assif O, Aviram H, Witz I P
Department of Cell Research and Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Israel.
Immunol Lett. 1995 Jan;44(2-3):209-12. doi: 10.1016/0165-2478(94)00216-e.
In previous studies non-lymphoid murine tumor cells were sorted by flow cytometry, into 2 subpopulations. The one expressed high levels of the T-cell activation protein Ly-6 A/E and the other low levels of this protein. High Ly-6 A/E expression was associated with very high tumorigenicity and metastatic phenotypes. Cells expressing low levels of this protein expressed a significantly reduced malignancy phenotype as compared to unsorted tumor populations. In view of its direct (or indirect) involvement in tumor progression we studied, in the present work, the regulation by microenvironmental factors of Ly-6 A/E expression on A3C polyoma-virus transformed cells. Ligation of membrane Ly-6 A/E by the corresponding monoclonal antibodies resulted in up-regulated expression of this protein. Similar results were obtained by exposing A3C cells to interferon-alpha. In contrast, exposing tumor cells to tumor necrosis factor-alpha or to the extracellular matrix protein laminin resulted in a down-regulation of Ly-6 A/E expression on these cells. These results provide an additional insight into the role microenvironmental factors might play in tumor progression.
在先前的研究中,非淋巴细胞性小鼠肿瘤细胞通过流式细胞术被分选成两个亚群。其中一个亚群表达高水平的T细胞活化蛋白Ly-6 A/E,另一个亚群表达低水平的该蛋白。高Ly-6 A/E表达与非常高的致瘤性和转移表型相关。与未分选的肿瘤群体相比,表达低水平该蛋白的细胞表现出显著降低的恶性表型。鉴于其直接(或间接)参与肿瘤进展,在本研究中,我们研究了微环境因素对A3C多瘤病毒转化细胞上Ly-6 A/E表达的调控。用相应的单克隆抗体连接膜Ly-6 A/E导致该蛋白表达上调。将A3C细胞暴露于α干扰素也获得了类似结果。相反,将肿瘤细胞暴露于肿瘤坏死因子-α或细胞外基质蛋白层粘连蛋白导致这些细胞上Ly-6 A/E表达下调。这些结果为微环境因素在肿瘤进展中可能发挥的作用提供了进一步的见解。