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首页> 外文期刊>Clinical & developmental immunology. >The Ability of Secretory Leukocyte Protease Inhibitor to Inhibit Apoptosis in Monocytes Is Independent of Its Antiprotease Activity
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The Ability of Secretory Leukocyte Protease Inhibitor to Inhibit Apoptosis in Monocytes Is Independent of Its Antiprotease Activity

机译:分泌型白细胞蛋白酶抑制剂抑制单核细胞凋亡的能力与其抗蛋白酶活性无关

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摘要

Secretory Leukocyte Protease Inhibitor (SLPI) is a serine protease inhibitor produced by epithelial and myeloid cells with anti-inflammatory properties. Research has shown that SLPI exerts its anti-inflammatory activity by directly binding to NF-kappaB DNA binding sites and, in so doing, prevents binding and subsequent transcription of proinflammatory gene expression. In the current study, we demonstrate that SLPI can inhibit TNF-alpha-induced apoptosis in U937 cells and peripheral blood monocytes. Specifically, SLPI inhibits TNF-alpha-induced caspase-3 activation and DNA degradation associated with apoptosis. We go on to show that this ability of SLPI to inhibit apoptosis is not dependent on its antiprotease activity as antiprotease deficient variants of SLPI can also inhibit TNF-alpha-induced apoptosis. This reduction in monocyte apoptosis may preserve monocyte function during inflammation resolution and promote infection clearance at mucosal sites.
机译:分泌型白细胞蛋白酶抑制剂(SLPI)是丝氨酸蛋白酶抑制剂,由具有抗炎特性的上皮细胞和髓样细胞产生。研究表明,SLPI通过直接结合NF-kappaB DNA结合位点发挥抗炎活性,并因此防止促炎基因表达的结合和随后的转录。在当前的研究中,我们证明SLPI可以抑制U937细胞和外周血单核细胞中TNF-α诱导的凋亡。具体而言,SLPI抑制TNF-α诱导的caspase-3活化和与细胞凋亡相关的DNA降解。我们继续表明,SLPI抑制凋亡的能力并不依赖于其抗蛋白酶活性,因为SLPI的抗蛋白酶缺陷型变体也可以抑制TNF-α诱导的凋亡。单核细胞凋亡的减少可以在炎症消退期间保留单核细胞功能,并促进粘膜部位的感染清除。

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