Phadke K, Nanda S
Clin Exp Immunol. 1983 Mar;51(3):494-500.
In this study, we have investigated the role of extracellular matrix components of connective tissue, collagen and proteoglycans, in the activation of rabbit macrophages and articular chondrocytes. Addition of type II collagen, in native or denatured form, or proteoglycan subunits, led to the activation of macrophages and release of chondrocyte stimulating factor. Type I collagen, when used at higher concentrations, was also capable of macrophage activation. The conditioned media of activated macrophages induced an increased protease synthesis by chondrocytes. Collagen or proteoglycan subunits did not have any direct stimulatory effect on chondrocytes. Intraperitoneal injections of collagen induced infiltration of macrophages into the peritoneal cavity. Although these macrophages failed to produce significant levels of chondrocyte stimulating factor by themselves, they could be activated in culture with lipopolysaccharides or collagen to produce chondrocyte stimulating factor. The chondrocytes, treated with the conditioned medium of activated macrophages (with lipopolysaccharides or cartilage matrix components), failed to survive in suspension cultures.
在本研究中,我们研究了结缔组织的细胞外基质成分——胶原蛋白和蛋白聚糖,在兔巨噬细胞和关节软骨细胞激活过程中的作用。添加天然或变性形式的II型胶原蛋白或蛋白聚糖亚基,会导致巨噬细胞的激活以及软骨细胞刺激因子的释放。当以较高浓度使用时,I型胶原蛋白也能够激活巨噬细胞。活化巨噬细胞的条件培养基可诱导软骨细胞增加蛋白酶的合成。胶原蛋白或蛋白聚糖亚基对软骨细胞没有任何直接刺激作用。腹腔注射胶原蛋白会诱导巨噬细胞浸润到腹腔中。尽管这些巨噬细胞自身无法产生显著水平的软骨细胞刺激因子,但它们在与脂多糖或胶原蛋白一起培养时可被激活,从而产生软骨细胞刺激因子。用活化巨噬细胞(与脂多糖或软骨基质成分一起)的条件培养基处理的软骨细胞,在悬浮培养中无法存活。