Etherington D J, Pugh D, Silver I A
Acta Biol Med Ger. 1981;40(10-11):1625-36.
Collagen degradation was investigated in experimental inflammatory lesions made by implanting fluorescein-collagen sponges into sensitised rats for four days, before transferring them into culture medium. The breakdown of the collagenous structure in vitro by invading cells was inhibited by steroids and related anti-inflammatory drugs whereas non-steroidal anti-inflammatory drugs were without effect. Inhibitors of the lysosomal proteinases were variably effective with chloroquine giving total inhibition, leupeptin and TLCK partial inhibition and aurothioglucose showing no effect. Histochemical studies were made of the distribution of cathepsin B. Beta-glucuronidase and N-acetyl-glucosaminidase in macrophages attached to a collagen substratum. Measurements with specific microelectrodes showed that the microenvironment at the surface of activated macrophages was markedly acidic with values of pH less than 5 between attached cells and collagen substratum. Such conditions would be hostile to neutral collagenases and favour acid (lysosomal) proteinases.
通过将荧光素 - 胶原海绵植入致敏大鼠体内四天,然后将其转移至培养基中,在实验性炎性病变中研究胶原降解情况。甾体类药物及相关抗炎药可抑制侵袭细胞在体外对胶原结构的破坏,而非甾体类抗炎药则无此作用。溶酶体蛋白酶抑制剂的效果各异,氯喹可完全抑制,亮抑酶肽和甲苯磺酰 - L - 赖氨酸氯甲基酮部分抑制,而金硫葡萄糖则无作用。对附着于胶原基质的巨噬细胞中组织蛋白酶B、β - 葡萄糖醛酸酶和N - 乙酰葡糖胺酶的分布进行了组织化学研究。用特定微电极测量表明,活化巨噬细胞表面的微环境明显呈酸性,附着细胞与胶原基质之间的pH值小于5。这种条件不利于中性胶原酶,而有利于酸性(溶酶体)蛋白酶。