Ghosh P, Collier S, Andrews J
J Rheumatol. 1987 May;14 Spec No:122-4.
Using a peritoneal macrophage/articular cartilage co-culture system, it was shown that the serine proteinase inhibitor derived from human articular cartilage modulated the release of 35S-labelled proteoglycan into media in a concentration dependent manner. Since the cartilage inhibitor fractions used were free of metallo-proteinase and cysteine proteinase inhibitory activity, but strongly inhibited serine proteinases, it was suggested that such enzymes may be implicated in the activation of latent metallo-proteoglycanases produced by chondrocytes on exposure to IL-1.
利用腹膜巨噬细胞/关节软骨共培养系统,研究发现源自人关节软骨的丝氨酸蛋白酶抑制剂以浓度依赖的方式调节35S标记的蛋白聚糖释放到培养基中。由于所使用的软骨抑制剂组分不含金属蛋白酶和半胱氨酸蛋白酶抑制活性,但能强烈抑制丝氨酸蛋白酶,因此有人提出,此类酶可能与软骨细胞在暴露于白细胞介素-1时产生的潜在金属蛋白聚糖酶的激活有关。