Abstract

This study attempts to characterize cystatin 10 (Cst10), which we recently identified as a novel protein implicated in endochondral ossification. Expression of Cst10 was specific to cartilage, localized in the cytosol of prehypertrophic and hypertrophic chondrocytes of the mouse growth plate. In the mouse chondrogenic cell line ATDC5, Cst10 expression preceded type X collagen expression and increased in synchrony with maturation. When we compared ATDC5 cells transfected with Cst10 cDNA with cells transfected with a mock vector, hypertrophic maturation and mineralization of chondrocytes were promoted by Cst10 gene overexpression in that type X collagen expression was observed earlier, and alizarin red staining was stronger. On the other hand, type II collagen expression and Alcian blue staining, both of which are markers of the early stage of chondrocyte differentiation, were similar in both cells. Overexpression of the Cst10 gene also caused fragmentation of nuclei, the appearance of annexin V, a change in the mitochondrial membrane potential, and activation of caspases. These results strongly suggest that Cst10 may play an important role in the last steps of the chondrocyte differentiation pathway as an inducer of maturation, followed by apoptosis of chondrocytes.

Highlights

  • This study attempts to characterize cystatin 10 (Cst10), which we recently identified as a novel protein implicated in endochondral ossification

  • When we compared ATDC5 cells transfected with Cst10 cDNA with cells transfected with a mock vector, hypertrophic maturation and mineralization of chondrocytes were promoted by Cst10 gene overexpression in that type X collagen expression was observed earlier, and alizarin red staining was stronger

  • Characterization of the Cst10 Gene—In a previous study, using differential display analysis, we identified nine genes, including Cst10, whose expression is regulated in the auricular cartilage of ttw mice fed a high phosphate diet (1)

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Summary

EXPERIMENTAL PROCEDURES

Determination of the Genomic Structure of the Mouse Cst Gene— Bacterial artificial chromosome (BAC) clones containing the mouse Cst gene were isolated using a BAC PCR screening system (Genome Systems, St. Louis, MO) according to the manufacturer’s protocol. The set of primers used for screening was Cst10/BAC/F (5Ј-TCCTGAGGATATATGTCAGGC-3Ј) and Cst10/BAC/R (5Ј-ATCTCTGTCTGAGGAAAGGAG-3Ј). To determine the size of introns of the Cst gene, interexon PCRs were carried out with primers designed according to the cDNA sequence we determined in this study. The BAC clones and PCR products were sequenced directly, and the exon-intron junctions were

The abbreviations used are
RESULTS
DISCUSSION
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