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源自c-fos诱导的软骨肿瘤的稳定小鼠软骨生成细胞系。

Stable murine chondrogenic cell lines derived from c-fos-induced cartilage tumors.

作者信息

Wang Z Q, Grigoriadis A E, Wagner E F

机构信息

Research Institute of Molecular Pathology, Vienna, Austria.

出版信息

J Bone Miner Res. 1993 Jul;8(7):839-47. doi: 10.1002/jbmr.5650080710.

Abstract

This study describes the detailed characterization of four murine chondrogenic cell lines (wT2-1, wT2-7, wT2-8, and wT2-9) that were isolated from a cartilage tumor induced by the protooncogene c-fos in chimeric mice. All cell lines are clonal and display a fibroblastic morphology with a doubling time of 1-2 days. Northern blot analysis demonstrated that in addition to expressing high levels of exogenous c-fos, all clones express varying levels of the cartilage marker gene type II collagen in addition to type I collagen. The clones also expressed high levels of the AP-1 genes c-jun and fra-1. The doubling times of these clones did not change over a period of 14 months in culture. Most importantly, however, expression of type II collagen was maintained in all cell lines for 8 months in culture, and two cell lines maintained type II collagen expression when analyzed after 14 months. Interestingly, type I collagen expression was lost after long-term culture. Following injection into syngeneic and nude mice, all cell lines formed tumors containing areas with the morphologic appearance of hyaline cartilage, indicating that these cell lines are chondrogenic. Thus, these stable murine chondrogenic cell lines provide a useful tool for studying the transcriptional control of cartilage-specific gene expression, as well as the growth control of chondrogenic cells.

摘要

本研究描述了从原癌基因c-fos诱导的嵌合小鼠软骨肿瘤中分离出的四种小鼠软骨生成细胞系(wT2-1、wT2-7、wT2-8和wT2-9)的详细特征。所有细胞系均为克隆性,呈成纤维细胞形态,倍增时间为1-2天。Northern印迹分析表明,除了高水平表达外源性c-fos外,所有克隆除了表达I型胶原蛋白外,还表达不同水平的软骨标记基因II型胶原蛋白。这些克隆还高水平表达AP-1基因c-jun和fra-1。在培养14个月的时间里,这些克隆的倍增时间没有变化。然而,最重要的是,所有细胞系在培养8个月时II型胶原蛋白的表达得以维持,在14个月后分析时,有两个细胞系仍维持II型胶原蛋白的表达。有趣的是,长期培养后I型胶原蛋白的表达消失。将这些细胞系注射到同基因和裸鼠体内后,所有细胞系都形成了含有具有透明软骨形态外观区域的肿瘤,这表明这些细胞系具有软骨生成能力。因此,这些稳定的小鼠软骨生成细胞系为研究软骨特异性基因表达的转录调控以及软骨生成细胞的生长调控提供了一个有用的工具。

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