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应用印迹细胞学评估人类眼睑缘上皮。

Assessing the human lid margin epithelium using impression cytology.

机构信息

School of Optometry and Vision Science, University of New South Wales, UNSW, Australia.

出版信息

Acta Ophthalmol. 2012 Nov;90(7):e547-52. doi: 10.1111/j.1755-3768.2012.02482.x. Epub 2012 Aug 3.

DOI:10.1111/j.1755-3768.2012.02482.x
PMID:22863209
Abstract

PURPOSE

To establish if impression cytology combined with histochemical and immunocytochemical staining can be used to assess epithelium of the human upper lid margin.

METHODS

Following an initial eye examination of 40 healthy subjects (19 soft contact lens wearers and 21 non-contact lens wearers, aged 18-57 years), lid margin staining was assessed with lissamine green using slit lamp biomicroscopy and graded (grade 0-3). Impression cytology of the upper lid margin of both eyes was collected, fixed and stained with periodic acid Schiff (PAS) and haematoxylin for cell morphology analysis (Nelson grade) or for immunocytochemistry (keratinization-related proteins: filaggrin, transglutaminase1 (TGase1) and cytokeratin 1/10).

RESULTS

In 57% of all subjects, grade 0 lissamine green staining showed a thin line (the Marx line), just posterior to the meibomian gland ducts. Grade 2 or 3 lissamine green staining was observed in 17% of all subjects. There was no difference between contact lens and non-contact lens wearers for lid margin staining or Nelson grade (p = 0.4, Fisher's exact test). PAS/haematoxylin staining and immunocytochemistry showed transition in epithelial cell morphology, with marginal conjunctival epithelium, mucocutaneous junction and squamous epithelium, adjacent to meibomian gland ducts. This transition in epithelium was associated with differential expression of keratinization-related proteins (filaggrin, cytokeratin 1/10 and TGase1).

CONCLUSION

Lid margin epithelium can be successfully sampled using impression cytology and further characterized using histochemistry and immunocytochemistry staining techniques. This approach can be applied to assess lid margin changes in conditions such as dry eye and meibomian gland dysfunction.

摘要

目的

确定印迹细胞学结合组织化学和免疫细胞化学染色是否可用于评估人类上眼睑缘的上皮细胞。

方法

对 40 名健康受试者(19 名软性隐形眼镜佩戴者和 21 名非隐形眼镜佩戴者,年龄 18-57 岁)进行初步眼部检查后,使用荧光素钠裂隙灯生物显微镜评估睑缘染色,并进行分级(0-3 级)。收集双眼上睑缘的印迹细胞学标本,固定后进行过碘酸雪夫(PAS)和苏木精染色,用于细胞形态分析(Nelson 分级)或免疫细胞化学(角蛋白相关蛋白:丝聚合蛋白、转谷氨酰胺酶 1(TGase1)和细胞角蛋白 1/10)。

结果

在所有受试者中,57%的人出现 0 级荧光素钠染色,表现为一条细线(马克思线),位于睑板腺导管的后部。17%的受试者出现 2 级或 3 级荧光素钠染色。接触镜和非接触镜佩戴者之间,睑缘染色或 Nelson 分级无差异(p=0.4,Fisher 确切检验)。PAS/苏木精染色和免疫细胞化学显示上皮细胞形态的过渡,边缘结膜上皮、黏膜交界处和鳞状上皮与睑板腺导管相邻。这种上皮细胞的过渡与角蛋白相关蛋白(丝聚合蛋白、细胞角蛋白 1/10 和 TGase1)的差异表达有关。

结论

印迹细胞学可成功地对眼睑缘上皮进行取样,并通过组织化学和免疫细胞化学染色技术进一步进行特征描述。这种方法可用于评估干眼症和睑板腺功能障碍等情况下的眼睑缘变化。

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