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Acquisition of high metastatic capacity after in vitro fusion of a nonmetastatic tumor line with a bone marrow-derived macrophage

机译:非转移性肿瘤系与骨髓巨噬细胞体外融合后获得高转移能力

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摘要

A low metastatic, thioguanine-resistant murine T lymphoma line (EbTGR) was hybridized in vitro, with the help of polyethylene glycol, with syngeneic bone marrow-derived macrophages. Two HAT-resistant hybrid lines (Eb-F1 and Eb-F2) were obtained from independent fusion cultures. A cytogenetic analysis revealed that most of the macrophage chromosomes except No. 12 had segregated or become rearranged 60 d after fusion, a time at which the cell lines had become stabilized in culture. Syngeneic mice inoculated subcutaneously with the tumor macrophage hybrid lines developed, very quickly, visceral metastases and died after less than 2 wk, while those inoculated with the parental line lived for greater than 6 wk and developed only localized, large primary tumors. The metastatic hybridomas expressed a similar tumor antigen as a spontaneous, in vivo derived, high metastatic variant (ESb) of the same tumor. This suggests that ESb cells might have arisen from a spontaneous fusion with a host macrophage.
机译:在聚乙二醇的帮助下,将低转移性,耐硫鸟嘌呤的鼠类T淋巴瘤系(EbTGR)与同源骨髓衍生的巨噬细胞进行体外杂交。从独立的融合培养物中获得了两个耐HAT的杂种系(Eb-F1和Eb-F2)。细胞遗传学分析显示,除第12号外,大多数巨噬细胞染色体在融合后60 d分离或重新排列,此时细胞系已在培养物中稳定下来。皮下接种肿瘤巨噬细胞杂交系的同系小鼠发展迅速,内脏转移并在少于2周后死亡,而接种亲本系的小鼠存活期超过6周,仅发展出局部的大型原发性肿瘤。转移性杂交瘤表达的肿瘤抗原与同一肿瘤的自发,体内衍生的高转移变体(ESb)类似。这表明ESb细胞可能来自与宿主巨噬细胞的自发融合。

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