Miller F R, McEachern D, Miller B E
E. Walter Albachten Department of Immunology, Michigan Cancer Foundation, Detroit 48201.
Cancer Res. 1989 Nov 1;49(21):6091-7.
We have reported previously that both normal mammary epithelium and stroma stimulate the growth of mouse mammary tumors in vivo. We have devised a method to investigate the role of diffusible factors in these growth interactions in vitro. Because an appropriate matrix, a particular cell shape, or multicellular organization may be required for the production of factors and/or for the response to such factors, the method assesses the expansion of boluses of cells in collagen gel matrix. Under these culture conditions, paracrine effects were detected which were not observed when cells were growing in monolayer on plastic. The growth of mammary tumor lines 66, 410.4, and D2A1 was stimulated by both mammary epithelial cells and fibroblasts prepared from midpregnant mouse mammary glands. In contrast, these mammary tumor lines were inhibited by coculturing with normal mammary cells in monolayer on plastic. Stimulation in collagen and inhibition in monolayer cultures were both dose dependent; increasing numbers of regulator mammary cells increased the effects on tumor growth. Additional tumor cells did not stimulate growth of target tumor cell boluses in collagen gel cultures. This attempt to model the in situ situation may be a more appropriate model for the detection and characterization of relevant diffusible growth regulatory factors than monolayers on plastic and/or colonies growing in agar.
我们之前曾报道,正常乳腺上皮和基质均可在体内刺激小鼠乳腺肿瘤的生长。我们设计了一种方法来研究体外这些生长相互作用中可扩散因子的作用。由于产生因子和/或对这些因子作出反应可能需要合适的基质、特定的细胞形状或多细胞组织,因此该方法评估细胞团在胶原凝胶基质中的扩增情况。在这些培养条件下,检测到了旁分泌效应,而当细胞在塑料上单层生长时未观察到这种效应。来自妊娠中期小鼠乳腺的乳腺上皮细胞和成纤维细胞均刺激了乳腺肿瘤细胞系66、410.4和D2A1的生长。相比之下,在塑料上单层培养时,这些乳腺肿瘤细胞系与正常乳腺细胞共培养会受到抑制。胶原培养中的刺激和单层培养中的抑制均呈剂量依赖性;调节性乳腺细胞数量增加会增强对肿瘤生长的影响。在胶原凝胶培养中,额外的肿瘤细胞不会刺激靶肿瘤细胞团的生长。与塑料上的单层培养和/或琼脂中生长的集落相比,这种模拟原位情况的尝试可能是检测和表征相关可扩散生长调节因子的更合适模型。