Settembre Carmine, Arteaga-Solis Emilio, McKee Marc D, de Pablo Raquel, Al Awqati Qais, Ballabio Andrea, Karsenty Gerard
Department of Genetics and Development, College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.
Genes Dev. 2008 Oct 1;22(19):2645-50. doi: 10.1101/gad.1711308.
Cartilage extracellular matrix (ECM) contains large amounts of proteoglycans made of a protein core decorated by highly sulfated sugar chains, the glycosaminoglycans (GAGs). GAGs desulfation, a necessary step for their degradation, is exerted by sulfatases that are activated by another enzyme, Sulfatase-Modifying Factor 1 (SUMF1), whose inactivation in humans leads to severe skeletal abnormalities. We show here that despite being expressed in both osteoblasts and chondrocytes Sumf1 does not affect osteoblast differentiation. Conversely, in chondrocytes it favors ECM production and autophagy and promotes proliferation and differentiation by limiting FGF signaling. Thus, proteoglycan desulfation is a critical regulator of chondrogenesis.
软骨细胞外基质(ECM)含有大量蛋白聚糖,这些蛋白聚糖由蛋白质核心和高度硫酸化的糖链(即糖胺聚糖,GAGs)修饰而成。GAGs的去硫酸化是其降解的必要步骤,由硫酸酯酶完成,而硫酸酯酶由另一种酶硫酸酯酶修饰因子1(SUMF1)激活,SUMF1在人类体内失活会导致严重的骨骼异常。我们在此表明,尽管Sumf1在成骨细胞和软骨细胞中均有表达,但它并不影响成骨细胞的分化。相反,在软骨细胞中,它有利于ECM的产生和自噬,并通过限制FGF信号促进细胞增殖和分化。因此,蛋白聚糖去硫酸化是软骨生成的关键调节因子。