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从可移植大鼠恶性纤维组织细胞瘤建立的克隆细胞系的异质性。

Heterogeneity of cloned cell lines established from a transplantable rat malignant fibrous histiocytoma.

作者信息

Yamate J, Tajima M, Togo M, Shibuya K, Ihara M, Kudow S

机构信息

Nippon Institute for Biological Science, Tokyo.

出版信息

Jpn J Cancer Res. 1991 Mar;82(3):298-307. doi: 10.1111/j.1349-7006.1991.tb01846.x.

Abstract

Four cloned cell lines, MT-7, MT-8, MT-9 and MT-10, were established from a transplantable malignant fibrous histiocytoma (MFH) of F344 rats to investigate the histogenesis of the tumor. Cells of MT-7, MT-9 and MT-10 had fine structures characteristic of histiocytes, such as numerous cell processes, many lysosomes and well-developed cytoplasmic organelles. They stained positively for histiocytic lysosomal and antigenic markers. In addition, MT-9 cells contained microfilaments and well-developed RER in their cytoplasm, suggesting that they may be facultative fibroblasts. MT-8 cells stained weakly for histiocytic markers and had scant cytoplasmic organelles. They were identified as undifferentiated mesenchymal cells. The tumors induced in syngeneic rats by inoculating MT-7 or MT-10 consisted of a mixture of the pleomorphic, myxoid and storiform types of MFH, and those by MT-9 were of the storiform type. Cells forming these tumors stained positively for histiocytic markers. Tumors induced by MT-8 consisted of undifferentiated cells negative to these stainings. The histogenesis of MFH is surmised to be related to various differentiation stages shifting from undifferentiated cells to histiocytic cells capable of acting as facultative fibroblasts.

摘要

从F344大鼠的可移植性恶性纤维组织细胞瘤(MFH)中建立了四个克隆细胞系,即MT-7、MT-8、MT-9和MT-10,以研究该肿瘤的组织发生。MT-7、MT-9和MT-10细胞具有组织细胞的精细结构特征,如众多细胞突起、许多溶酶体和发达的细胞质细胞器。它们对组织细胞溶酶体和抗原标志物呈阳性染色。此外,MT-9细胞的细胞质中含有微丝和发达的粗面内质网,提示它们可能是兼性成纤维细胞。MT-8细胞对组织细胞标志物染色较弱,细胞质细胞器稀少。它们被鉴定为未分化的间充质细胞。通过接种MT-7或MT-10在同基因大鼠中诱导产生的肿瘤由多形性、黏液样和席纹状类型的MFH混合组成,而MT-9诱导产生的肿瘤为席纹状类型。形成这些肿瘤的细胞对组织细胞标志物呈阳性染色。MT-8诱导产生的肿瘤由对这些染色呈阴性的未分化细胞组成。推测MFH的组织发生与从未分化细胞到能够作为兼性成纤维细胞的组织细胞的各种分化阶段有关。

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本文引用的文献

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Spontaneous rat malignant tumors of fibrohistiocytic origin: an ultrastructural study.
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