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SERPINA3 is a marker of cartilage differentiation and is essential for the expression of extracellular matrix genes during early chondrogenesis

软骨发生 细胞外基质 硫氧化物9 阿格里坎 软骨细胞 软骨寡聚基质蛋白 基因 软骨 细胞生物学 基因表达 细胞分化 生物 II型胶原 分子生物学 间充质干细胞 遗传学 化学 骨关节炎 解剖 病理 医学 关节软骨 替代医学
作者
Matthew J. Barter,David A. Turner,Sarah J. Rice,Mary Hines,Hua Lin,Adrian M. D. Falconer,Euan McDonnell,Jamie Soul,María del Carmen Arques,G. Nicholas Europe‐Finner,Andrew D. Rowan,David A. Young,D. Wilkinson
出处
期刊:Matrix Biology [Elsevier BV]
卷期号:133: 33-42 被引量:1
标识
DOI:10.1016/j.matbio.2024.07.004
摘要

Serine proteinase inhibitors (serpins) are a family of structurally similar proteins which regulate many diverse biological processes from blood coagulation to extracellular matrix (ECM) remodelling. Chondrogenesis involves the condensation and differentiation of mesenchymal stem cells (MSCs) into chondrocytes which occurs during early development. Here, and for the first time, we demonstrate that one serpin, SERPINA3 (gene name SERPINA3, protein also known as alpha-1 antichymotrypsin), plays a critical role in chondrogenic differentiation. We observed that SERPINA3 expression was markedly induced at early time points during in vitro chondrogenesis. We examined the expression of SERPINA3 in human cartilage development, identifying significant enrichment of SERPINA3 in developing cartilage compared to total limb, which correlated with well-described markers of cartilage differentiation. When SERPINA3 was silenced using siRNA, cartilage pellets were smaller and contained lower proteoglycan as determined by dimethyl methylene blue assay (DMMB) and safranin-O staining. Consistent with this, RNA sequencing revealed significant downregulation of genes associated with cartilage ECM formation perturbing chondrogenesis. Conversely, SERPINA3 silencing had a negligible effect on the gene expression profile during osteogenesis suggesting the role of SERPINA3 is specific to chondrocyte differentiation. The global effect on cartilage formation led us to investigate the effect of SERPINA3 silencing on the master transcriptional regulator of chondrogenesis, SOX9. Indeed, we observed that SOX9 protein levels were markedly reduced at early time points suggesting a role for SERPINA3 in regulating SOX9 expression and activity. In summary, our data support a non-redundant role for SERPINA3 in enabling chondrogenesis via regulation of SOX9 levels.
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