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基质金属蛋白酶有助于调节新型隐球菌感染中的趋化因子表达和肺部炎症。

Matrix metalloproteinases contribute to the regulation of chemokine expression and pulmonary inflammation in Cryptococcus infection.

作者信息

Supasorn O, Sringkarin N, Srimanote P, Angkasekwinai P

机构信息

Department of Medical Technology, Faculty of Allied Health Sciences.

Graduate Program in Biomedical Science, Faculty of Allied Health Sciences, Thammasat University, Pathumthani, Thailand.

出版信息

Clin Exp Immunol. 2016 Mar;183(3):431-40. doi: 10.1111/cei.12725. Epub 2015 Nov 24.

Abstract

Matrix metalloproteinases (MMPs) are a family of extracellular proteases that play roles in regulating the immune response in inflammatory processes. Previous studies indicated that different MMPs were involved in the host defence and tissue damage in response to different pathogens. However, the contributions of MMPs during Cryptococcus infection have not been addressed clearly. Here, we examined the expression and activity of MMPs during Cryptococcus infection. Among MMP family members, we found significant increases of MMP-3 and MMP-12 mRNA levels and MMP12 zymographic activities in response to C. neoformans but not C. gattii infection. The expression of MMP12 was induced in RAW cells after C. neoformans treatment and in alveolar macrophages purified from C. neoformans-infected mice. Interestingly, administration of MMP inhibitor GM6001 into C. neoformans-infected mice resulted in a significantly increased pulmonary fungal burden with attenuated inflammatory cell infiltration. Corresponding to this finding, the expression of the macrophage- and neutrophil-attracting chemokines CCL2 and CXCL1 was inhibited in the GM6001-treated group and MMP12 levels were found to be correlated strongly with CCL2 mRNA expression. Thus, our data suggest that the induction of MMPs by C. neoformans infection potentiates inflammatory cell infiltration by modulating pulmonary chemokines, thereby promoting effective host immunity to pulmonary Cryptococcus infection.

摘要

基质金属蛋白酶(MMPs)是一类细胞外蛋白酶家族,在炎症过程中调节免疫反应发挥作用。先前的研究表明,不同的MMPs参与了对不同病原体的宿主防御和组织损伤。然而,MMPs在新型隐球菌感染过程中的作用尚未明确阐述。在此,我们检测了新型隐球菌感染过程中MMPs的表达和活性。在MMP家族成员中,我们发现新型隐球菌感染而非格特隐球菌感染后,MMP-3和MMP-12的mRNA水平以及MMP12的酶谱活性显著增加。新型隐球菌处理后,RAW细胞以及从新型隐球菌感染小鼠中纯化的肺泡巨噬细胞中MMP12的表达被诱导。有趣的是,对新型隐球菌感染的小鼠给予MMP抑制剂GM6001后,肺部真菌负荷显著增加,炎症细胞浸润减弱。与此发现一致,GM6001处理组中巨噬细胞和中性粒细胞趋化因子CCL2和CXCL1的表达受到抑制,且发现MMPs水平与CCL2 mRNA表达密切相关。因此,我们的数据表明,新型隐球菌感染诱导MMPs通过调节肺部趋化因子增强炎症细胞浸润,从而促进宿主对肺部新型隐球菌感染的有效免疫。

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