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体内浸润并破坏肿瘤多细胞球体的细胞的形态学和功能特征。

Morphological and functional characteristics of cells infiltrating and destroying tumor multicellular spheroids in vivo.

作者信息

Lord E M, Penney D P, Sutherland R M, Cooper R A

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1979 Oct;31(2):103-16. doi: 10.1007/BF02889928.

Abstract

EMT6 mammary sarcoma cells were grown in vitro as multicellular spheroids to model for the heterogeneity of microenvironments and structural changes which develop in many tumors, including micrometastases. Spheroids of 700-900 micron diameter were implanted into and recovered at different times from the peritoneal cavities of sensitized or nonsensitized allogeneic and syngeneic mice. The colony forming efficiency of spheroid tumor cells recovered at 24 and 48 h from sensitized allogeneic mice was markedly decreased as compared with those from nonsensitized allogeneic or syngeneic animals. These recovered spheroids were extensively infiltrated by both lymphocytes and macrophages, which ultrastructurally had very close membrane associations with tumor cells. Host cells recovered from spheroids exhibited cytotoxic activity in an in vitro 51Cr release assay. Thus, multicellular spheroids in vivo provide a unique experimental model to study the functional capacity of host cells within a spheroical tumor. Although lacking the stroma and the vasculature of in vivo solid tumors, this model does have many similarities to in vivo tumors and is thus suitable for studying the tumor cell-host cell interactions within the tumor microenvironment. In addition, the system offers the potential for quantitative study of the effects of treatment modalities on tumor cell-host cell interactions.

摘要

EMT6乳腺肉瘤细胞在体外培养成多细胞球体,以模拟许多肿瘤(包括微转移瘤)中出现的微环境异质性和结构变化。将直径700 - 900微米的球体植入致敏或未致敏的同种异体和同基因小鼠的腹腔,并在不同时间回收。与从未致敏的同种异体或同基因动物回收的球体肿瘤细胞相比,从致敏同种异体小鼠在24小时和48小时回收的球体肿瘤细胞的集落形成效率明显降低。这些回收的球体被淋巴细胞和巨噬细胞广泛浸润,从超微结构来看,它们与肿瘤细胞有非常紧密的膜关联。从球体回收的宿主细胞在体外51Cr释放试验中表现出细胞毒性活性。因此,体内多细胞球体为研究球形肿瘤内宿主细胞的功能能力提供了一个独特的实验模型。尽管缺乏体内实体瘤的基质和脉管系统,但该模型与体内肿瘤有许多相似之处,因此适合研究肿瘤微环境内的肿瘤细胞 - 宿主细胞相互作用。此外,该系统为定量研究治疗方式对肿瘤细胞 - 宿主细胞相互作用的影响提供了潜力。

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