Hypertrophic Chondrocytes

Гипертрофические хондроциты
Phoebe S. Leboy, Irving M. Shapiro, Maurizio Pacifici, Eleanor B. Golden, Osamu Oshima, Sherrill Adams
1990-08-01

endochondral ossificationhypertrophic chondrocytesproteoglycan core proteintype II collagentype X collagen
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.
1
Based on observed gene expression changes and Holtzer's cell lineage definition, hypertrophic chondrocytes are concluded to represent the terminal differentiation stage of the chondrogenic lineage.
2
Hypertrophic chondrocytes arise after a phase of active proliferation during endochondral ossification and show marked quantitative and qualitative changes in gene expression.
3
Osteonectin is produced across resting, proliferating, and hypertrophic zones but is scarce and cell-associated in early zones and abundant and matrix-associated in the hypertrophic zone.
4
Proteoglycan core protein mRNA levels increase in regions of cartilage destined for endochondral ossification.
5
Type II collagen mRNA increases markedly in proliferating chondrocytes and returns to basal levels in hypertrophic chondrocytes.
6
Type X collagen mRNA is undetectable in resting and early proliferating chondrocytes but is detectable in hypertrophic chondrocytes.

Hypertrophic chondrocytes in chicken tibial growth cartilage during endochondral ossification

Developmental position and phenotypic/gene-expression changes (extracellular matrix genes: proteoglycan core protein, type II collagen, type X collagen, osteonectin) of hypertrophic chondrocytes during endochondral ossification

Publication Details
Publication Date
1990-08-01
Journal
Publisher
ISSN
Access Type
Author Information
Authors
Phoebe S. Leboy
Irving M. Shapiro
Maurizio Pacifici
Eleanor B. Golden
Osamu Oshima
Sherrill Adams
Explore further
Open the scid.ai AI chat with a ready-made request: it will find papers on a similar topic and help build a literature review.
Find similar papers in the chat
Make a presentation
100%