Enhancement of rat ACT-1 tumor clonogenicity by xenogeneic mouse macrophages.

In Vitro Pub Date : 1984-08-01 DOI:10.1007/BF02619611
K W Beagley, L S Horne, R F Noronha, C M Goodall, C M Moore
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Abstract

In vitro growth of rat atriocaval epithelial tumor cells (ACT-1) was enhanced by the inclusion of xenogeneic mouse adherent peritoneal exudate cells (PECs) in a two-layer soft agar system. A linear relationship was found between the number of cells plated and the number of colonies when ACT-1 tumor cells were plated at plating densities of between 1 and 5 X 10(5) cell/60 mm plate (r = 0.9, P less than 0.001). Inclusion of irradiated PECs in the bioassay for tumor stem cells resulted in a two and a half-fold increase in colony formation in three separate experiments (P less than 0.001).

异种小鼠巨噬细胞增强大鼠ACT-1肿瘤的克隆性。
将异种小鼠黏附腹膜渗出细胞(PECs)包埋在双层软琼脂体系中,可以促进大鼠心房上皮肿瘤细胞(ACT-1)的体外生长。当ACT-1肿瘤细胞在1 ~ 5 × 10(5)个细胞/60 mm板的密度下,细胞数与菌落数呈线性关系(r = 0.9, P < 0.001)。在三个独立的实验中,将辐照后的PECs纳入肿瘤干细胞的生物测定,导致集落形成增加2.5倍(P < 0.001)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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