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首页> 外文期刊>Investigative ophthalmology & visual science >The role of Mannose Receptor during Aspergillus fumigatus infection and the interaction with Dectin-1 in Corneal Epithelial Cells
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The role of Mannose Receptor during Aspergillus fumigatus infection and the interaction with Dectin-1 in Corneal Epithelial Cells

机译:甘露糖受体在烟曲霉感染中的作用以及与角膜上皮细胞中Dectin-1的相互作用

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Purpose : To investigate the expression and function of Mannose Receptor (MR) and explore its interaction with Dectin-1 in human corneal epithelial cells (HCECs) exposed to Aspergillus fumigatus (A. fumigatus). Methods : HCECs were stimulated with A. fumigatus for 0???4, 8, 12, 16 and 24 hours. MR expression was tested by PCR, western-blot and immunohistochemistry. HCECs were pretreated with 2ug/ml MR blocking antibody and expression of p38, phosphorylated p38 (p-p38), the downstream cytokines ???TNF-?±, IL-1?2??? and Dectin-1 were tested by PCR, western-blot and ELISA. HCECs were pretreated with Dectin-1 agonists (curdlan, 100ug/ml) and inhibitors (laminarin, 10ug/ml) and expression of MR was tested. Results : MR expression was up-regulated after stimulated with A. fumigatus. MR mRNA and protein began to rise at 8 hours and 16 hours respectively. Stronger immunostaining of MR was observed in fungal infected corneal epithelium than in normal corneal epithelium. A. fumigates increased production of TNF-?± (11-, 4-fold of control), IL-1?2 (4.7-, 3-fold of control), p-p38 (2.1-fold of control) and Dectin-1 (2.3-, 2-fold of control) in mRNA and protein levels. MR antibody significantly suppressed the expression of TNF-?± (28%, 50% reduction), IL-1?2 (38%, 42% reduction), p-p38 (38% reduction) and Dectin-1 (48%, 47% reduction). Curdlan increased production of MR (1.5-, 1.9-fold of control) while laminarin decreased MR expression (50%, 60% reduction) induced by A. fumigatus. Conclusions : HCECs express MR and A. fumigates infection can increase MR expression. A. fumigates induce the expression of inflammatory cytokines via MR and p38 MAPK pathway. The expression of Dectin-1 and MR had mutual influence. This is an abstract that was submitted for the 2016 ARVO Annual Meeting, held in Seattle, Wash., May 1-5, 2016.
机译:目的:研究甘露糖受体(MR)的表达和功能,并探讨其与Dectin-1在暴露于烟曲霉(A. fumigatus)的人角膜上皮细胞(HCEC)中的相互作用。方法:用烟曲霉刺激HCEC 0、4、8、12、16和24小时。通过PCR,蛋白质印迹和免疫组织化学测试MR表达。用2ug / ml MR阻断抗体预处理HCEC,并表达p38,磷酸化p38(p-p38),下游细胞因子TNF-α±,IL-1β2。 PCR,Western-blot和ELISA检测Dectin-1和Dectin-1。 HCEC用Dectin-1激动剂(curdlan,100ug / ml)和抑制剂(laminarin,10ug / ml)预处理,并测试了MR的表达。结果:烟曲霉刺激后,MR表达上调。 MR mRNA和蛋白质分别在8小时和16小时开始上升。在真菌感染的角膜上皮中观察到比正常角膜上皮中的MR更强的免疫染色。 A.熏蒸增加了TNF-α±(11-,对照的4倍),IL-1β2(4.7-,对照的3倍),p-p38(对照2.1-​​)和Dectin-的产量。 mRNA和蛋白质水平为1(对照组的2.3倍)。 MR抗体可显着抑制TNF-α±(降低28%,降低50%),IL-1β2(降低38%,降低42%),p-p38(降低38%)和Dectin-1(降低48%)的表达。减少47%)。 Curdlan增加了MR的产生(是对照的1.5倍,1.9倍),而laminarin降低了由烟曲霉诱导的MR表达(减少了50%,60%)。结论:HCECs表达MR和熏蒸曲霉感染可以增加MR表达。熏蒸曲霉通过MR和p38 MAPK途径诱导炎性细胞因子的表达。 Dectin-1和MR的表达相互影响。这是提交给2016年5月1-5日在华盛顿州西雅图市举行的2016 ARVO年会的摘要。

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