Pacifici M, Golden E B, Oshima O, Shapiro I M, Leboy P S, Adams S L
Department of Anatomy-Histology, School of Dental Medicine, University of Pennsylvania, Philadelphia 19104.
Ann N Y Acad Sci. 1990;599:45-57. doi: 10.1111/j.1749-6632.1990.tb42363.x.
Chondrocytes emerging in the limb or other locations during embryogenesis are currently considered terminally differentiated cells and thus represent the last stage of differentiation in the chondrogenic cell lineage. Most chondrocytes, however, undergo further major phenotypic changes during late embryogenesis and early postnatal life as they take part in the endochondral ossification process. During this process, "resting" chondrocytes first enter an active, proliferative phase and then develop into large, round hypertrophic chondrocytes with unique phenotypic traits. The question thus arises as to whether hypertrophic chondrocytes actually represent the terminal stage of differentiation in the chondrogenic lineage. To assess the developmental position of these cells along the lineage, we examined the expression of four genes encoding extracellular matrix components in chondrocytes undergoing endochondral ossification in chicken tibial growth cartilage. We found that the steady-state levels of mRNAs coding for proteoglycan core protein increased in regions of cartilage destined for endochondral ossification. Similarly, type II collagen gene expression increased markedly in proliferating chondrocytes and then returned to basal levels in hypertrophic chondrocytes. As revealed by in situ hybridization, type X collagen gene expression was undetectable in resting and early proliferating chondrocytes and was detectable in hypertrophic chondrocytes. Osteonectin synthesis appeared to characterize chondrocytes in the resting, proliferating, and hypertrophic zones of growth cartilage. The protein was scarce, however, and cell-associated in the former zones, although it was very abundant and matrix-associated in the hypertrophic zone. Clearly, the emergence of hypertrophic chondrocytes during endochondral ossification is accompanied by marked quantitative and qualitative changes in gene expression. Interestingly, these changes occur during or immediately after the period of active chondrocyte proliferation. On the premises of the cell lineage definition proposed by Holtzer, the above data suggest that the hypertrophic chondrocytes represent the terminal stage of differentiation in the chondrogenic cell lineage.
在胚胎发育过程中出现在肢体或其他部位的软骨细胞目前被认为是终末分化细胞,因此代表软骨形成细胞谱系分化的最后阶段。然而,大多数软骨细胞在胚胎后期和出生后早期会经历进一步的主要表型变化,因为它们参与软骨内成骨过程。在此过程中,“静止”的软骨细胞首先进入活跃的增殖阶段,然后发育成具有独特表型特征的大的圆形肥大软骨细胞。因此,问题就出现了,肥大软骨细胞是否真的代表软骨形成谱系分化的终末阶段。为了评估这些细胞在谱系中的发育位置,我们检测了鸡胫骨生长软骨中经历软骨内成骨的软骨细胞中四个编码细胞外基质成分的基因的表达。我们发现,编码蛋白聚糖核心蛋白的mRNA的稳态水平在注定要进行软骨内成骨的软骨区域增加。同样,II型胶原基因表达在增殖的软骨细胞中显著增加,然后在肥大软骨细胞中恢复到基础水平。原位杂交显示,X型胶原基因表达在静止和早期增殖的软骨细胞中不可检测,而在肥大软骨细胞中可检测到。骨连接蛋白的合成似乎是生长软骨静止、增殖和肥大区域软骨细胞的特征。然而,该蛋白在前两个区域稀少且与细胞相关,而在肥大区域非常丰富且与基质相关。显然,软骨内成骨过程中肥大软骨细胞的出现伴随着基因表达的显著定量和定性变化。有趣的是,这些变化发生在软骨细胞活跃增殖期期间或之后不久。根据霍尔特泽提出的细胞谱系定义,上述数据表明肥大软骨细胞代表软骨形成细胞谱系分化的终末阶段。