首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Anionic glycoconjugates from differentiated and dedifferentiated cultures of bovine articular chondrocytes: modulation by TGF-beta.
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Anionic glycoconjugates from differentiated and dedifferentiated cultures of bovine articular chondrocytes: modulation by TGF-beta.

机译:牛关节软骨细胞分化和去分化培养物中的阴离子糖缀合物:由TGF-β调节。

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摘要

Primary, high density bovine articular chondrocyte (BAC) cultures, stimulated with transforming growth factor-beta-1, elaborated a high molecular weight anionic glycoconjugate, kDa 540, which does not contain glycosaminoglycan chains (Chan and Anastassiades, 1996). The effect of exogenously added transforming growth factor-beta-1 on the elaboration of the high molecular weight glycoconjugate and of proteoglycans was studied during dedifferentiation of the chondrocytes, utilizing a serial subculture technique under anchorage-dependent conditions, up to four subcultures. The high molecular weight glycoconjugate was detected in the media of all growth-factor-stimulated chondrocyte subcultures, as well as stimulated primary cultures, but not in unstimulated primary cultures or subcultures. By contrast, a large proteoglycan, was only secreted by primary cultures and first subcultures, whether treated with transforming growth factor-beta-1 or untreated. This proteoglycan contained mostly chondroitin sulfate chains, whose hydrodynamic size was increased by the addition of transforming growth factor-beta-1. Further, the pattern of the proteoglycans appearing in the media of subcultures 2-4 was influenced by the addition of transforming growth factor-beta-1, so that while these control subcultures elaborated both the large and small chondroitin sulfate proteoglycans, the equivalent stimulated subcultures elaborated only intermediate sized chondroitin sulfate proteoglycan(s). These results suggest that while dedifferentiation of articular chondrocytes, achieved by subculturing, strongly modulates the effect of exogenously added transforming growth factor-beta-1 on the type of proteoglycan elaborated, the process of dedifferentiation does not influence the transforming-growth-factor-beta-dependent synthesis of the high molecular weight anionic glycoconjugate.
机译:用转化生长因子-β-1刺激的原发性高密度牛关节软骨细胞(BAC)培养物制成了不包含糖胺聚糖链的高分子量阴离子糖缀合物kDa 540(Chan和Anastassiades,1996)。研究了外源添加的转化生长因子-β-1对软骨细胞去分化过程中高分子量糖缀合物和蛋白聚糖加工的影响,利用锚定依赖性条件下的连续传代培养技术,最多进行了四个传代培养。在所有生长因子刺激的软骨细胞继代培养物以及经刺激的原代培养物的培养基中均检测到了高分子量的糖缀合物,但未刺激的原代培养物或亚培养物中未检测到高分子量的糖缀合物。相比之下,无论是用转化生长因子-β-1处理还是未经处理,大型蛋白聚糖仅由原代培养物和初次培养物分泌。这种蛋白聚糖主要含有硫酸软骨素链,其流体动力学大小因添加转化生长因子-β-1而增加。此外,添加转化生长因子-β-1影响了在亚培养2-4培养基中出现的蛋白聚糖的模式,因此,尽管这些对照亚培养都对硫酸软骨素大小蛋白聚糖进行了详细说明,但同等刺激的亚培养仅阐述了中等尺寸的硫酸软骨素蛋白聚糖。这些结果表明,虽然通过传代培养实现的关节软骨细胞去分化强烈调节了外源添加的转化生长因子-β-1对蛋白聚糖类型的影响,但去分化过程并不影响转化生长因子-β。依赖性的高分子量阴离子糖缀合物的合成。

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