Solursh M, Karp G C
J Exp Zool. 1975 Jan;191(1):73-84. doi: 10.1002/jez.1401910108.
In this report an autoradiographic approach is used to compare synthetic activities of cells within differentiated cartilage colonies. While amino acid incorporation is umiform throughout the colony, H-3-uridine is incorporated more actively by cells having little matrix, cells which are typically in the peripheral regions of a colony. On the other hand S-35-O4 is incorporated most actively by cells in the colony centers. This difference in sulfation appears to occur independently of the mitotic state of the cells, since it is apparent in both growing and near-stationary cultures. Instead, there is a correlation between the accumulation of extracellular matrix and more active levels of sulfation. In support of the idea that matrix creates a microenvironment more favorable to chondrogenesis is the observation that a brief treatment with hyaluronidase, which removes about 60% of the S-35-O4 from prelabeled cultures, depresses isolation of labeled glycosaminoglycans. The possible role of extracellular matrices in altering the expression of differentiated functions by creating a more favorable microenvironment is considered.
在本报告中,采用放射自显影方法比较分化软骨集落内细胞的合成活性。虽然整个集落中氨基酸掺入是均匀的,但H-3-尿苷在几乎没有基质的细胞中掺入更活跃,这些细胞通常位于集落的周边区域。另一方面,S-35-O4在集落中心的细胞中掺入最活跃。这种硫酸化差异似乎独立于细胞的有丝分裂状态而发生,因为在生长培养物和接近静止的培养物中都很明显。相反,细胞外基质的积累与更高的硫酸化活性水平之间存在相关性。支持基质创造更有利于软骨形成的微环境这一观点的是以下观察结果:用透明质酸酶进行短暂处理,可从预标记培养物中去除约60%的S-35-O4,这会抑制标记糖胺聚糖的分离。细胞外基质通过创造更有利的微环境来改变分化功能表达的可能作用也被考虑在内。