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受麻风分枝杆菌刺激产生基质金属蛋白酶的许旺细胞可能在麻风性神经病的结果中发挥作用。

Schwann cells producing matrix metalloproteinases under Mycobacterium leprae stimulation may play a role in the outcome of leprous neuropathy.

机构信息

Leprosy Laboratory, Oswaldo Cruz Institute, Rio de Janeiro, Brazil.

出版信息

J Neuropathol Exp Neurol. 2010 Jan;69(1):27-39. doi: 10.1097/NEN.0b013e3181c6515c.

Abstract

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.

摘要

基质金属蛋白酶(MMPs)在周围神经病变中介导脱髓鞘和血神经屏障的破坏。研究了分枝杆菌麻风分枝杆菌和肿瘤坏死因子(TNF)刺激的人施万细胞系 ST88-14 细胞中的基质金属蛋白酶和组织金属蛋白酶抑制剂 1 基因表达和分泌,以及神经麻风病患者(n=21)和非麻风病对照者(n=3)的神经活检。分枝杆菌麻风分枝杆菌和 TNF 诱导 MMP-2 和 MMP-9 的上调,并增加培养的 ST88-14 细胞中这些酶的分泌。TNF 和 M. leprae 的作用具有协同作用,抗 TNF 抗体阻断部分抑制了这种协同作用。具有炎症浸润和纤维化的神经显示出比对照更高的 TNF、MMP-2 和 MMP-9 mRNA。没有炎症改变的麻风神经活检也表现出更高的 MMP-2 和 MMP-9;纤维化和炎症活检中的组织金属蛋白酶抑制剂 1 明显升高。神经的免疫组织化学双重标记表明 MMP 主要由巨噬细胞和施万细胞表达。具有神经内膜炎症浸润和上皮样肉芽肿的活检显示出最高水平的 MMP-2 和 MMP-9 mRNA。总之,这些结果表明,M. leprae 和 TNF 可能直接诱导施万细胞上调并分泌 MMPs,而与麻风神经病变中的炎症程度无关。

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