首页> 美国卫生研究院文献>Biochemical Journal >Regulation of type-II collagen gene expression during human chondrocyte de-differentiation and recovery of chondrocyte-specific phenotype in culture involves Sry-type high-mobility-group box (SOX) transcription factors.
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Regulation of type-II collagen gene expression during human chondrocyte de-differentiation and recovery of chondrocyte-specific phenotype in culture involves Sry-type high-mobility-group box (SOX) transcription factors.

机译:人类软骨细胞去分化和培养过程中软骨细胞特异性表型恢复过程中II型胶原基因表达的调节涉及Sry型高迁移率族盒(SOX)转录因子。

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摘要

During ex vivo growth as monolayer cultures, chondrocytes proliferate and undergo a process of de-differentiation. This process involves a change in morphology and a change from expression of chondrocyte-specific genes to that of genes that are normally expressed in fibroblasts. Transfer of the monolayer chondrocyte culture to three-dimensional culture systems induces the cells to re-acquire a chondrocyte-specific phenotype and produce a cartilaginous-like tissue in vitro. We investigated mechanisms involved in the control of the de-differentiation and re-differentiation process in vitro. De-differentiated chondrocytes re-acquired their chondrocyte-specific phenotype when cultured on poly-(2-hydroxyethyl methacrylate) (polyHEMA) as assayed by morphology, reverse transcriptase PCR of chondrocyte-specific mRNA, Western-blot analysis and chondrocyte-specific promoter activity. Essentially, full recovery of the chondrocyte-specific phenotype was observed when cells that had been cultured for 4 weeks on plastic were transferred to culture on polyHEMA. However, after subsequent passages on plastic, the phenotype recovery was incomplete or did not occur. The activity of a gene reporter construct containing the promoter and enhancer from the human type-II collagen gene (COL2A1) was modulated by the culture conditions, so that its transcriptional activity was repressed in monolayer cultures and rescued to some extent when the cells were switched to polyHEMA cultures. The binding of Sry-type high-mobility-group box (SOX) transcription factors to the enhancer region was modulated by the culture conditions, as were the mRNA levels for SOX9. A transfected human type-II collagen reporter construct was activated in de-differentiated cells by ectopic expression of SOX transcription factors. These results underscore the overt change in phenotype that occurs when chondrocytes are cultured as monolayers on tissue-culture plastic substrata.
机译:在单层培养的离体生长过程中,软骨细胞增殖并经历去分化过程。该过程涉及形态改变和从软骨细胞特异性基因的表达到成纤维细胞中正常表达的基因的表达的改变。将单层软骨细胞培养物转移至三维培养系统会诱导细胞重新获得软骨细胞特异性表型,并在体外产生软骨样组织。我们调查了参与体外去分化和再分化过程控制的机制。去分化的软骨细胞在聚甲基丙烯酸2-羟乙酯(polyHEMA)上培养时重新获得了其软骨细胞特异性表型,通过形态学,软骨细胞特异性mRNA的逆转录酶PCR,Western印迹分析和软骨细胞特异性启动子活性进行了测定。本质上,将已经在塑料上培养了4周的细胞转移到polyHEMA上的培养物中,可以观察到软骨细胞特异性表型的完全恢复。然而,在塑料上的后续传代后,表型恢复不完全或没有发生。通过培养条件来调节含有人类II型胶原基因的启动子和增强子的基因报告基因构建体(COL2A1)的活性,从而在单层培养中抑制其转录活性,并在切换细胞时在一定程度上得以拯救到polyHEMA文化。 Sry型高迁移率族盒(SOX)转录因子与增强子区域的结合受培养条件的调节,SOX9的mRNA水平也受其调节。通过异位表达SOX转录因子,可在去分化细胞中激活转染的人类II型胶原报告基因构建体。这些结果强调了当软骨细胞在组织培养塑料基质上单层培养时发生的表型的明显变化。

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