Chacko S, Abbott J, Holtzer S, Holtzer H
J Exp Med. 1969 Aug 1;130(2):417-42. doi: 10.1084/jem.130.2.417.
A single, functional, mitotically quiescent chondrocyte may be induced to reenter the mitotic cyde, and produce a progeny of over 10(11) cells. Sessile, adherent, polygonal cells deposit matrix, whereas amoeboid, dispersed, flattened fibroblastic cells do not. The prior synthetic history of a cell is of greater importance in determining whether the characteristic chondrogenic phenotype will be expressed, rather than growth in "permissive" or "nonpermissive" medium. Clonal conditions select for stem-like cells, some of whose progeny may become polygonal chondrocytes. The retention of the characteristic chondrogenic phenotype in vitro is favored by pruning the dedifferentiated chondrocytes which arise in these cultures. Dedifferentiated chondrocytes interfere with the deposition and synthesis of chondroitin sulfate by neighboring functional chondrocytes. Possible mechanisms are proposed to explain this type of cell-cell or cell exudate interference. If the progeny of a single, genetically programmed chondrocyte may or may not synthesize chondroitin sulfate, then extragenic sites in the cytoplasm or cell surface must influence the decision as to which cluster of "luxur" molecules the cell will synthesize.
单个具有功能的、处于有丝分裂静止期的软骨细胞可能被诱导重新进入有丝分裂周期,并产生超过10¹¹个细胞的后代。固着的、贴壁的多边形细胞会沉积基质,而变形虫样的、分散的、扁平的成纤维细胞则不会。细胞先前的合成历史在决定是否会表达特征性软骨生成表型方面比在“允许性”或“非允许性”培养基中生长更为重要。克隆条件会选择干细胞样细胞,其一些后代可能会变成多边形软骨细胞。通过去除这些培养物中出现的去分化软骨细胞,有利于在体外保留特征性软骨生成表型。去分化软骨细胞会干扰相邻功能性软骨细胞对硫酸软骨素的沉积和合成。提出了可能的机制来解释这种细胞间或细胞分泌物干扰类型。如果单个经过基因编程的软骨细胞的后代可能合成也可能不合成硫酸软骨素,那么细胞质或细胞表面的基因外位点必定会影响细胞将合成哪一组“奢侈”分子的决定。