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三维胶原凝胶培养中小鼠乳腺肿瘤亚群之间的代谢合作

Metabolic cooperation between mouse mammary tumor subpopulations in three-dimensional collagen gel cultures.

作者信息

Miller B E, McInerney D, Jackson D, Miller F R

出版信息

Cancer Res. 1986 Jan;46(1):89-93.

PMID:3940214
Abstract

A series of subpopulation lines derived from a single mouse mammary tumor were tested for their ability to interact with each other in metabolic cooperation assays in three-dimensional collagen gel cultures. Inhibition of growth in the presence of selective drug (6-thioguanine or 2-fluoroadenine) of two 6-thioguanine-resistant cell lines, 66cl4 and 44FTO, as well as a 2-fluoroadenine-resistant line, 168FAR, occurred in the presence of other sensitive cells, demonstrating the transfer of drug sensitivity to drug-resistant cells. Transfer of drug resistance was shown by using selective medium containing hypoxanthine, aminopterin, and thymidine plus ouabain in which mutual metabolic cooperation between line 66cl4 (also ouabain resistant) and "wild-type" lines is required for growth. Effective communication leading to the transfer of drug resistance and ultimate survival of both cell types occurred in mixtures containing as little as 10% of either cell type. The requirement for mutual metabolic cooperation in hypoxanthine, aminopterin, and thymidine plus ouabain medium prevented line 66 from overgrowing line 66cl4 to the extent that it did in control medium. The ranked abilities of lines 66, 410.4, and 168 to promote growth when mixed with line 66cl4 in collagen cultures in hypoxanthine, aminopterin, and thymidine plus ouabain medium were correlated with the ranked cell densities required for these same cell lines to inhibit growth of line 66cl4 by metabolic cooperation in the presence of 6-thioguanine in monolayer cultures. These ranked abilities may be related to the effectiveness with which each of these cell lines is able to form communicating junctions with line 66cl4.

摘要

从单个小鼠乳腺肿瘤衍生出一系列亚群细胞系,在三维胶原凝胶培养中进行代谢合作试验,测试它们相互作用的能力。在选择性药物(6-硫鸟嘌呤或2-氟腺嘌呤)存在下,两种6-硫鸟嘌呤抗性细胞系66cl4和44FTO以及一种2-氟腺嘌呤抗性细胞系168FAR的生长受到抑制,这发生在存在其他敏感细胞的情况下,表明药物敏感性从敏感细胞转移到了耐药细胞。通过使用含有次黄嘌呤、氨基蝶呤和胸腺嘧啶核苷加哇巴因的选择性培养基来显示耐药性的转移,在这种培养基中,66cl4细胞系(也对哇巴因耐药)与“野生型”细胞系之间的相互代谢合作是生长所必需的。在含有低至10%任何一种细胞类型的混合物中,发生了导致耐药性转移和两种细胞类型最终存活的有效通讯。在次黄嘌呤、氨基蝶呤和胸腺嘧啶核苷加哇巴因培养基中对相互代谢合作的需求,阻止了66细胞系过度生长超过66cl4细胞系,而在对照培养基中则会出现这种过度生长的情况。在胶原培养中,当66、410.4和168细胞系与66cl4细胞系在次黄嘌呤、氨基蝶呤和胸腺嘧啶核苷加哇巴因培养基中混合时,促进生长的能力排名,与这些相同细胞系在单层培养中在6-硫鸟嘌呤存在下通过代谢合作抑制66cl4细胞系生长所需的细胞密度排名相关。这些排名能力可能与这些细胞系中每一个与66cl4细胞系形成通讯连接的有效性有关。

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