Lennon D P, Osdoby P, Carrino D A, Vertel B M, Caplan A I
J Craniofac Genet Dev Biol. 1983;3(3):235-51.
This communication describes a replating technique for the separation of the chondrogenic and non-chondrogenic cells from stage-24 chick limb bud mesenchymal cell cultures by means of sequential digestion with collagenase. Four sub-populations of cells were obtained: The first consisted solely of non-chondrocytes and the next three were progressively enriched in chondrocytes. In addition to morphological differences, the four cell populations differed from each other in their rates of incorporation of sulfate into macromolecular material which were roughly proportional to the percentage of chondrocytes. The chondrocytes and non-chondrocytes no longer exhibited a density dependence of phenotype. In addition, the normal multilayered nodular morphology associated with cartilage development was not observed. These isolated cells have been used as starting material for detailed biochemical studies. Together, these studies indicate that the expressional program governing biosynthetic changes in chondrocytes is not controlled by the extracellular matrix.
本通讯描述了一种再接种技术,该技术通过用胶原酶顺序消化,从第24期鸡胚肢芽间充质细胞培养物中分离软骨生成细胞和非软骨生成细胞。获得了四个细胞亚群:第一个亚群仅由非软骨细胞组成,接下来的三个亚群软骨细胞逐渐富集。除了形态学差异外,这四个细胞群体在将硫酸盐掺入大分子物质的速率上也彼此不同,其速率大致与软骨细胞的百分比成正比。软骨细胞和非软骨细胞不再表现出表型的密度依赖性。此外,未观察到与软骨发育相关的正常多层结节形态。这些分离的细胞已被用作详细生化研究的起始材料。总之,这些研究表明,控制软骨细胞生物合成变化的表达程序不受细胞外基质的控制。