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首页> 外文期刊>Journal of Neuropathology and Experimental Neurology >Schwann Cells Producing Matrix Metalloproteinases Under Mycobacterium leprae Stimulation May Play a Role in the Outcome of Leprous Neuropathy
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Schwann Cells Producing Matrix Metalloproteinases Under Mycobacterium leprae Stimulation May Play a Role in the Outcome of Leprous Neuropathy

机译:雪旺细胞在麻风分枝杆菌刺激下产生基质金属蛋白酶可能在麻风神经病的结果中起作用

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摘要

Matrix metalloproteinases (MMPs) mediate demyelination and breakdown of the blood-nerve barrier in peripheral neuropathies. Matrix metalloproteinases and tissue inhibitor of metalloproteinase 1 gene expression and secretion were studied in cells of the human Schwann cell line ST88-14 stimulated with Mycobacterium leprae and tumor necrosis factor (TNF) and in nerve biopsies from patients with neural leprosy (n = 21) and nonleprous controls (n = 3). Mycobacterium leprae and TNF induced upregulation of MMP-2 and MMP-9 and increased secretion of these enzymes in cultured ST88-14 cells. The effects of TNF and M. leprae were synergistic, and anti-TNF antibody blockage partially inhibited this synergistic effect. Nerves with inflammatory infiltrates and fibrosis displayed higher TNF, MMP-2, and MMP-9 mRNA than controls. Leprous nerve biopsies with no inflammatory alterations also exhibited higher MMP-2 and MMP-9; tissue inhibitor of metalloproteinase 1 was significantly higher in biopsies with fibrosis and inflammation. Immunohistochemical double labeling of the nerves demonstrated that the MMPs were mainly expressed by macrophages and Schwann cells. The biopsies with endoneurial inflammatory infiltrates and epithelioid granulomas had the highest levels of MMP-2 and MMP-9 mRNA detected. Together, these results suggest that M. leprae and TNF may directly induce Schwann cells to upregulate and secrete MMPs regardless of the extent of inflammation in leprous neuropathy.
机译:基质金属蛋白酶(MMP)介导周围神经病变中的脱髓鞘和血神经屏障的破坏。在麻风分枝杆菌和肿瘤坏死因子(TNF)刺激的人类雪旺氏细胞ST88-14细胞和神经麻风病患者的神经活检中研究了基质金属蛋白酶和金属蛋白酶1组织抑制剂的表达和分泌和非麻痹性对照(n = 3)。麻风分枝杆菌和TNF诱导MMP-2和MMP-9上调,并在培养的ST88-14细胞中增加这些酶的分泌。 TNF和麻风分枝杆菌具有协同作用,而抗TNF抗体的阻滞可部分抑制这种协同作用。具有炎性浸润和纤维化的神经表现出比对照组更高的TNF,MMP-2和MMP-9 mRNA。没有炎性改变的麻风神经活检也显示出较高的MMP-2和MMP-9;在具有纤维化和炎症的活检组织中,金属蛋白酶1的组织抑制剂明显更高。神经的免疫组织化学双重标记表明,MMPs主要由巨噬细胞和雪旺氏细胞表达。具有神经内膜炎性浸润和上皮样肉芽肿的活检组织中检出的MMP-2和MMP-9 mRNA最高。总之,这些结果表明,不管麻风神经病的炎症程度如何,麻风分枝杆菌和TNF均可直接诱导雪旺细胞上调和分泌MMP。

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