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建立具有软骨表型的克隆性人软骨肉瘤细胞系。

Establishment of a clonal human chondrosarcoma cell line with cartilage phenotypes.

作者信息

Takigawa M, Tajima K, Pan H O, Enomoto M, Kinoshita A, Suzuki F, Takano Y, Mori Y

机构信息

Department of Biochemistry, Osaka University Faculty of Dentistry, Japan.

出版信息

Cancer Res. 1989 Jul 15;49(14):3996-4002.

PMID:2736538
Abstract

A clonal cell line with cartilage phenotypes and tumorigenicity during more than 3 years in culture was established from a human chondrosarcoma. In sparse cultures, the clonal line, named HCS-2/8, consisted of slightly elongated polygonal cells, which proliferated with a doubling time of 3.5 days. The cells became polygonal to spherical as they became confluent. After reaching confluence, the cells continued to proliferate slowly and formed nodules, which showed metachromasia when stained with toluidine blue. The nodules were three-dimensional in structure; cells were multilayered in the surface regions, overlying a thick layer of extracellular matrix, which showed metachromasia. Electron microscopically, the cells resembling chondrocytes in vivo were surrounded by an extracellular matrix consisting of thin collagen-like fibrils with numerous fine granules, presumably of proteoglycans. The cells actively synthesized proteoglycans as determined by [35S]sulfate incorporation. The hydrodynamic size of major proteoglycan monomers synthesized by the cells was that of so-called cartilage-specific proteoglycans, as determined by glycerol gradient centrifugation. Immunostaining identified type II collagen but not type I collagen. Fluorography and immunoblotting of collagens separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis also demonstrated the synthesis of type II collagen but not type I collagen. Inoculation of HCS-2/8 cells into athymic mice resulted in the formation of chondrosarcomas that resembled the original tumor. Because of having these characters, HCS-2/8 cells should be useful not only in studies on the differentiated phenotypes of human chondrocytes but also in basic studies on the diagnosis, treatment, and etiology of human chondrosarcomas.

摘要

从人软骨肉瘤中建立了一种在培养超过3年的具有软骨表型和致瘤性的克隆细胞系。在稀疏培养中,名为HCS-2/8的克隆细胞系由略呈细长形的多边形细胞组成,其倍增时间为3.5天。细胞汇合时从多边形变为球形。汇合后,细胞继续缓慢增殖并形成结节,用甲苯胺蓝染色时呈异染性。结节呈三维结构;细胞在表面区域多层排列,覆盖着一层厚厚的细胞外基质,也呈异染性。电子显微镜下,类似于体内软骨细胞的细胞被细胞外基质包围,该基质由薄的胶原样纤维和许多细颗粒组成,推测为蛋白聚糖。通过[35S]硫酸盐掺入法测定,这些细胞能活跃地合成蛋白聚糖。通过甘油梯度离心法测定,细胞合成的主要蛋白聚糖单体的流体动力学大小为所谓的软骨特异性蛋白聚糖。免疫染色鉴定出II型胶原,但未鉴定出I型胶原。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分离胶原后的荧光显影和免疫印迹也证明了II型胶原而非I型胶原的合成。将HCS-2/8细胞接种到无胸腺小鼠体内会导致形成类似于原始肿瘤的软骨肉瘤。由于具有这些特性,HCS-2/8细胞不仅在人类软骨细胞分化表型的研究中有用,而且在人类软骨肉瘤的诊断、治疗和病因学的基础研究中也有用。

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