Department of Pediatrics, Division of Pediatric Endocrinology, The Warren Alpert Medical School of Brown University and Hasbro Children's Hospital, Providence, RI, United States of America.
Department of Orthopedics, The Warren Alpert Medical School of Brown University, Providence, RI, United States of America.
PLoS One. 2019 Jun 17;14(6):e0218399. doi: 10.1371/journal.pone.0218399. eCollection 2019.
Aggrecan is an integral component of the extracellular matrix in cartilaginous tissues, including the growth plate. Heterozygous defects in the aggrecan gene have been identified as a cause of autosomal dominant short stature, bone age acceleration, and premature growth cessation. The mechanisms accounting for this phenotype remain unknown. We used ATDC5 cells, an established model of chondrogenesis, to evaluate the effects of aggrecan deficiency. ATDC5 aggrecan knockdown cell lines (AggKD) were generated using lentiviral shRNA transduction particles. Cells were stimulated with insulin/transferrin/selenium for up to 21 days to induce chondrogenesis. Control ATDC5 cells showed induction of Col2a1 starting at day 8 and induction of Col10a1 starting at day 12. AggKD cells had significantly reduced expression of Col2a1 and Col10a1 (p<0.0001) with only minimal increases in expression over time, indicating that chondrogenesis was markedly impaired. The induction of Col2a1 and Col10a1 was not rescued by culturing of AggKD cells in wells pre-conditioned with ATDC5 extracellular matrix or in co-culture with wild-type ATDC5 cells. We interpret our studies as indicating that aggrecan has an integral role in chondrogenesis that may be mediated through intracellular mechanisms.
聚集蛋白聚糖是软骨组织细胞外基质的组成部分,包括生长板。聚集蛋白聚糖基因的杂合缺陷已被确定为常染色体显性身材矮小、骨龄加速和过早生长停止的原因。导致这种表型的机制尚不清楚。我们使用 ATDC5 细胞,一种已建立的软骨生成模型,来评估聚集蛋白聚糖缺乏的影响。使用慢病毒 shRNA 转导颗粒生成 ATDC5 聚集蛋白聚糖敲低细胞系 (AggKD)。用胰岛素/转铁蛋白/硒刺激细胞长达 21 天以诱导软骨生成。对照 ATDC5 细胞在第 8 天开始诱导 Col2a1 的表达,在第 12 天开始诱导 Col10a1 的表达。AggKD 细胞的 Col2a1 和 Col10a1 表达显著降低(p<0.0001),随着时间的推移仅略有增加,表明软骨生成明显受损。在预先用 ATDC5 细胞外基质包被的孔中培养 AggKD 细胞或与野生型 ATDC5 细胞共培养并不能挽救 Col2a1 和 Col10a1 的诱导。我们的研究表明,聚集蛋白聚糖在软骨生成中具有不可或缺的作用,这可能是通过细胞内机制介导的。