Vaes G
Agents Actions. 1980 Dec;10(6):474-85. doi: 10.1007/BF02024145.
Cell and tissue culture techniques provide valuable tools for investigating cell-to-cell interactions leading to the secretion of connective-tissue degrading enzymes, collagenase and proteoglycan-degrading neutral proteases, in inflammatory situations. These interactions, which might constitute a major regulatory mechanism, are reviewed here. Taken together, the available data strongly suggest that fibroblasts and related mesenchymal cells (such as chondrocytes, fibroblast-like or type B synovial lining cells, corneal stromal cells, etc.) could be the main suppliers of collagenase within tissues. These cells can secrete collagenase in response to factors produced by other cells, mainly macrophages and related cells (monocytes, synovial cells - presumably the macrophage like, type A synovial lining cells), possibly also epithelial cells. Lymphocytes are able to modulate factor production by macrophages so that, through the macrophage link the secretory behavior of the fibroblastic cells may be under the control of the immune defense system and serve as an effector of immune reactions leading to connective tissue destruction.
细胞和组织培养技术为研究在炎症情况下导致结缔组织降解酶(胶原酶和蛋白聚糖降解中性蛋白酶)分泌的细胞间相互作用提供了有价值的工具。本文综述了这些可能构成主要调节机制的相互作用。综合现有数据强烈表明,成纤维细胞和相关间充质细胞(如软骨细胞、成纤维细胞样或B型滑膜衬里细胞、角膜基质细胞等)可能是组织内胶原酶的主要来源。这些细胞可响应其他细胞产生的因子分泌胶原酶,这些其他细胞主要是巨噬细胞及相关细胞(单核细胞、滑膜细胞——可能是巨噬细胞样的A型滑膜衬里细胞),上皮细胞也可能参与。淋巴细胞能够调节巨噬细胞的因子产生,因此,通过巨噬细胞的联系,成纤维细胞的分泌行为可能受免疫防御系统的控制,并作为导致结缔组织破坏的免疫反应的效应器。