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Evaluation of ocular surface disorders: a new diagnostic tool based on impression cytology and confocal laser scanning microscopy.

机译:眼表疾病的评估:一种基于印象细胞学和共聚焦激光扫描显微镜的新型诊断工具。

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AIM: To provide a new tool for the evaluation of altered ocular surfaces by using a combination of impression cytology, laser scanning confocal microscopy and advanced image analysis. METHODS: The expression of keratin 3 (K3), keratin 12 (K12), keratin 19 (K19) and mucin 1 (MUC1) was analysed by immunofluorescence on both histological sections of nine corneoscleral buttons from normal donors comprising conjunctiva, limbus and cornea and impression cytology specimens from six healthy normal subjects (12 eyes) and 12 patients with chronic ocular surface disorders. Levels of fluorescence expression of the different markers were quantified through quantitative fluorescence immunohistochemistry (Q-FIHC). RESULTS: Impression cytology specimens from normal and diseased ocular surfaces showed distinct expression patterns for K12 and MUC1. Healthy corneas expressed only K12 (but not MUC1), while conjunctivalised corneas from patients with limbal stem cell deficiency (LSCD) were characterised by the presence of MUC1 and the disappearance of K12. Similar clear-cut results were not seen with the K3/K19 markers, which showed lack of specificity and overlapping signals in cornea and conjunctiva impression cytology specimens. CONCLUSIONS: The ability of K12 and of the antibody against MUC1 to discriminate clearly between limbus/cornea and conjunctiva in impression cytology specimens could become a valuable diagnostic tool for ophthalmologists in order to evaluate alterations of the ocular surface and the grading of LSCD.
机译:目的:通过结合印模细胞学,激光扫描共聚焦显微镜和高级图像分析,为评估眼表改变提供一种新工具。方法:通过免疫荧光分析了正常结膜,角膜缘,角膜缘和角膜缘供体的九个角膜巩膜纽扣的两个组织学切片,通过免疫荧光分析了角蛋白3(K3),角蛋白12(K12),角蛋白19(K19)和粘蛋白1(MUC1)的表达。来自六名健康正常受试者(12眼)和12位慢性眼表疾病患者的印象细胞学标本。通过定量荧光免疫组织化学(Q-FIHC)定量不同标志物的荧光表达水平。结果:正常和患病眼表的印象细胞学标本显示出不同的K12和MUC1表达模式。健康的角膜仅表达K12(而不表达MUC1),而来自角膜缘干细胞缺乏症(LSCD)患者的结膜化角膜以MUC1的存在和K12的消失为特征。用K3 / K19标记没有看到类似的清晰结果,这表明在角膜和结膜印模细胞学标本中缺乏特异性和信号重叠。结论:在印模细胞学标本中,K12和抗MUC1抗体清楚区分角膜缘/角膜和结膜的能力可能成为眼科医生评估眼表改变和LSCD分级的有价值的诊断工具。

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