Suppr超能文献

通过蛋白聚糖分析确定,鸡软骨细胞在长期悬浮培养中具有稳定的表型表达。

Stable phenotypic expression by chick chondroblasts in long-term suspension cultures as determined by proteoglycan analysis.

作者信息

Pacifici M, Oettinger H F

出版信息

Exp Cell Res. 1985 Dec;161(2):381-92. doi: 10.1016/0014-4827(85)90095-3.

Abstract

The influence of cell shape on phenotypic expression was studied in chick vertebral chondroblasts maintained for several weeks in suspension culture. To monitor phenotypic expression, synthesis of proteoglycans was studied in cultures of freshly-isolated 1-day-old chondroblasts and 1-to-6-week-old chondroblasts. The rate of proteoglycan synthesis was virtually identical in 1-week or older chondroblasts; however, this rate was 3- to 5-fold higher than in 1-day-old cells. When compared to the latter cells, the various populations of older chondroblasts synthesized monomers of the major cartilage proteoglycan (KS: CS-PG) of slightly lower molecular size and a lower level of unsubstituted N-acetylgalactosamine residues on their core protein but with similar chondroitin sulfate chains and levels of O-linked oligosaccharides. At no time of culture were changes in the proportions of the major vs the minor cartilage proteoglycans detected. The results suggest that in contrast to epithelioid chondroblasts in standard monolayer cultures studied previously, the round floating chondroblasts express very stable biosynthetic properties for a prolonged time in suspension. The distinct biosynthetic properties of 1-day-old chondroblasts are discussed in terms of an initial, transitory response to the culture condition and in relation to regulatory mechanisms for proteoglycan elaboration.

摘要

在悬浮培养中维持数周的鸡椎体软骨细胞中研究了细胞形状对表型表达的影响。为监测表型表达,在新鲜分离的1日龄软骨细胞和1至6周龄软骨细胞培养物中研究了蛋白聚糖的合成。1周龄或更大的软骨细胞中蛋白聚糖合成速率实际上相同;然而,该速率比1日龄细胞高3至5倍。与后者细胞相比,不同群体的老龄软骨细胞合成的主要软骨蛋白聚糖(KS:CS-PG)单体分子大小略低,核心蛋白上未取代的N-乙酰半乳糖胺残基水平较低,但硫酸软骨素链和O-连接寡糖水平相似。在培养的任何时候都未检测到主要与次要软骨蛋白聚糖比例的变化。结果表明,与先前研究的标准单层培养中的上皮样软骨细胞相反,圆形漂浮软骨细胞在悬浮中长时间表达非常稳定的生物合成特性。从对培养条件的初始短暂反应以及与蛋白聚糖合成的调节机制相关的角度讨论了1日龄软骨细胞独特的生物合成特性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验