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首页> 外文期刊>Archivum immunologiae et therapiae experimentalis >Macrophage Phenotype in the Ocular Surface of Experimental Murine Dry Eye Disease
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Macrophage Phenotype in the Ocular Surface of Experimental Murine Dry Eye Disease

机译:实验性小鼠干眼病眼表巨噬细胞表型

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To evaluate the phenotype of macrophages in the cornea and conjunctiva of C57BL/6 mice with induced experimental dry eye. C57BL/6 mice exposed to desiccating stress (DS) were evaluated at 1, 5, and 10 days and C57BL/6 mice maintained in non-stressed environment were used as controls. Whole eyes and adnexa were excised for histology or used for gene expression analysis. Location and phenotype of macrophages infiltrating the cornea and conjunctiva was evaluated by immunofluorescence analysis. Quantitative polymerase chain reaction evaluated macrophage markers and T cell-related and inflammatory cytokine expression in cornea and conjunctiva. Immunofluorescence staining demonstrated that macrophages reside in the conjunctiva of control and dry eye mice and their number did not change with DS. Real-time RT-PCR demonstrated that the level of M1 macrophage marker, iNOS, increased prominently in the conjunctiva at DS 10 days. In contrast, there was a non-significant decrease of the M2 marker Arg1 with DS. The levels of inflammatory cytokine, IL-12a mRNA transcript in the conjunctiva increased significantly at DS1 and decreased at DS5, while levels of IL-18 were significantly increased at DS 10. Macrophages reside in the ocular surface tissues of C57BL/6 mice. Although the number of macrophages in the conjunctiva does not change, evidence of inflammatory M1 activation after desiccating stress was observed. Better understanding of phagocyte diversity and activation in dry eye disease provide a basis for the development of phagocyte-targeted therapeutic strategies.
机译:为了评估诱导实验性干眼的C57BL / 6小鼠角膜和结膜中巨噬细胞的表型。在第1、5和10天评估暴露于干燥应激(DS)的C57BL / 6小鼠,将保持在非应激环境中的C57BL / 6小鼠用作对照。切除全眼和附件以进行组织学检查或用于基因表达分析。通过免疫荧光分析评估浸润角膜和结膜的巨噬细胞的位置和表型。定量聚合酶链反应评估了角膜和结膜中的巨噬细胞标志物以及T细胞相关和炎性细胞因子的表达。免疫荧光染色表明巨噬细胞存在于对照组和干眼小鼠的结膜中,并且其数目并未随DS而改变。实时逆转录-聚合酶链反应(RT-PCR)表明,DS第10天时,结膜中M1巨噬细胞标志物iNOS的水平显着增加。相反,与DS相比,M2标记Arg1的下降不显着。结膜中炎性细胞因子,IL-12a mRNA转录水平在DS1处显着增加,在DS5处降低,而在DS 10处IL-18水平显着增加。巨噬细胞位于C57BL / 6小鼠的眼表组织中。尽管结膜中巨噬细胞的数量没有变化,但在干燥压力后观察到炎症性M1激活的证据。对干眼病中吞噬细胞多样性和激活的更好理解为发展以吞噬细胞为目标的治疗策略提供了基础。

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