Gelatinase Contributes to the Degradation of Glomerular Basement Membrane Collagen by Human Neutrophils

Margret C.M. Vissers , Christine C. Winterbourn
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引用次数: 32

Abstract

Neutrophils contain a number of proteinases active at neutral pH which are able todegrade extracellular matrices. We have determined the contribution of the major neutral proteinases to human neutrophil-mediated degradation of glomerular basement membrane type IV collagen in an in vitro model of immune complex-induced injury. Studies with proteinase inhibitors showed that with intact neutrophils stimulated by immune complexes trapped within the basement membrane, approximately 70% of the degradation was due to serine proteinases and 30% to metalloproteinases. Identical results were obtained with cell-free medium containing neutrophil granule contents. Elastase accounted for almost all the digestion by serine proteinases with a minimal contribution by cathepsin G. All the metalloproteinase activity was due to gelatinase rather than collagenase, and purified gelatinase was also shown to degrade basement membrane collagen. Hence, gelatinase has activity against type IV collagen and may be able to degrade collagens not cleaved by specific collagenases.

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明胶酶参与人中性粒细胞对肾小球基底膜胶原蛋白的降解
中性粒细胞含有许多在中性pH下具有活性的蛋白酶,它们能够降解细胞外基质。在免疫复合物诱导的体外损伤模型中,我们确定了主要中性蛋白酶对人中性粒细胞介导的肾小球基底膜IV型胶原蛋白降解的贡献。对蛋白酶抑制剂的研究表明,被困在基底膜内的免疫复合物刺激的完整中性粒细胞,大约70%的降解是由于丝氨酸蛋白酶,30%是由于金属蛋白酶。在含中性粒细胞颗粒的无细胞培养基中得到相同的结果。丝氨酸蛋白酶几乎全部由弹性酶消化,组织蛋白酶g的贡献最小。所有的金属蛋白酶活性都是由明胶酶而不是胶原酶产生的,纯化的明胶酶也能降解基膜胶原。因此,明胶酶对IV型胶原具有活性,并且可能能够降解未被特定胶原酶裂解的胶原。
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