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眼表疾病的评估:一种基于印迹细胞学和共焦激光扫描显微镜的新型诊断工具。

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

机构信息

The Veneto Eye Bank Foundation, Venice, Italy.

出版信息

Br J Ophthalmol. 2010 Jul;94(7):926-32. doi: 10.1136/bjo.2009.164152. Epub 2009 Sep 8.

DOI:10.1136/bjo.2009.164152
PMID:19740872
Abstract

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.

摘要

目的

利用印迹细胞学、激光扫描共聚焦显微镜和先进的图像分析相结合,为评估眼表面改变提供一种新的工具。

方法

对来自 9 例正常供体(包括结膜、角膜缘和角膜)的角膜 - 巩膜纽扣的组织切片以及 6 例健康正常受试者(12 只眼)和 12 例慢性眼表面疾病患者的印迹细胞学标本进行角蛋白 3(K3)、角蛋白 12(K12)、角蛋白 19(K19)和黏蛋白 1(MUC1)的免疫荧光分析。通过定量荧光免疫组织化学(Q-FIHC)对不同标志物的荧光表达水平进行量化。

结果

正常和病变眼表面的印迹细胞学标本显示出 K12 和 MUC1 的明显表达模式。健康角膜仅表达 K12(不表达 MUC1),而来自角膜缘干细胞缺乏症(LSCD)患者的结膜化角膜则以 MUC1 的存在和 K12 的消失为特征。K3/K19 标志物则没有出现如此清晰的结果,其在角膜和结膜印迹细胞学标本中缺乏特异性且存在重叠信号。

结论

K12 和针对 MUC1 的抗体在印迹细胞学标本中能够清楚地区分角膜缘/角膜和结膜的能力,可能成为眼科医生评估眼表面改变和 LSCD 分级的有价值的诊断工具。

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