Herman J H, Greenblatt D, Khosla R C, Appel A M
Arthritis Rheum. 1984 Jan;27(1):79-91. doi: 10.1002/art.1780270113.
Nonenzymatic, trypsin sensitive cytokines derived from lectin stimulated normal human mononuclear cells have been shown to induce release of proteoglycan and collagen degrading proteinase activity from chondrocytes in cartilage organ and isolated suspension culture systems. Active chondrocyte protein and RNA synthesis were required to induce activity. Cytokines responsible were of both monocyte and T cell origin. Direct monokine catabolic induction and monokine/lectin-triggered lymphokine inducing activity could be demonstrated. Cyclooxygenase inhibitors and direct or indirect modulation of mononuclear cell or chondrocyte cAMP levels had no effect on factor synthesis or activity. Hydrocortisone abrogated the effect. Cytokines responsible were heat labile, unaffected by reduction/alkylation or neuraminidase exposure, and stable over a pH range of 3-10.
来源于凝集素刺激的正常人单核细胞的非酶促、对胰蛋白酶敏感的细胞因子,已被证明能在软骨器官和分离的悬浮培养系统中诱导软骨细胞释放蛋白聚糖和胶原蛋白降解蛋白酶活性。诱导活性需要活跃的软骨细胞蛋白质和RNA合成。起作用的细胞因子来源于单核细胞和T细胞。可证明有直接的单核因子分解代谢诱导作用以及单核因子/凝集素触发的淋巴因子诱导活性。环氧化酶抑制剂以及对单核细胞或软骨细胞cAMP水平的直接或间接调节对因子合成或活性没有影响。氢化可的松消除了这种作用。起作用的细胞因子对热不稳定,不受还原/烷基化或神经氨酸酶处理的影响,并且在pH值3至10的范围内稳定。