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通过二次谐波产生成像显微镜识别大疱性角膜病变角膜中基质结构的异常。

Abnormalities of stromal structure in the bullous keratopathy cornea identified by second harmonic generation imaging microscopy.

机构信息

Department of Ophthalmology, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi, Japan.

出版信息

Invest Ophthalmol Vis Sci. 2012 Jul 27;53(8):4998-5003. doi: 10.1167/iovs.12-10214.

Abstract

PURPOSE

To identify structural alterations in collagen lamellae and the transdifferentiation of keratocytes into myofibroblasts in the corneal stroma of bullous keratopathy (BK) patients and to examine the relation of such changes to the duration of stromal edema or the underlying cause of BK.

METHODS

Six normal human corneas and 16 BK corneas were subjected to second harmonic generation (SHG) imaging microscopy to allow three-dimensional (3-D) reconstruction of collagen lamellae. Expression of α-smooth muscle actin (αSMA) was examined by immunofluorescence analysis and conventional laser confocal microscopy.

RESULTS

Collagen lamellae were interwoven at the anterior stroma and uniformly aligned at the posterior stroma, whereas αSMA was not detected throughout the entire stroma of the normal cornea. Nine (56%) and 7 (44%) of the 16 BK corneas showed abnormal collagen structure at the anterior and posterior stroma, respectively. Expression of αSMA was detected in the anterior or posterior stroma of 7 (44%) and 6 (38%) of the 16 BK corneas, respectively. Disorganization of collagen lamellae and myofibroblastic transdifferentiation were detected only in corneas with a duration of stromal edema of at least 12 months. Corneas with BK as a result of birth injury showed abnormal collagen structure at the posterior stroma, whereas those with BK resulting from laser iridotomy did not.

CONCLUSIONS

Changes in the structure of the entire stroma were detected in BK corneas with a duration of stromal edema of at least 12 months, suggesting that such changes may be progressive. In addition, the underlying cause of BK may influence structural changes at the posterior stroma.

摘要

目的

鉴定大疱性角膜病变(BK)患者角膜基质中胶原板层的结构改变和角膜基质细胞向肌成纤维细胞的转分化,并探讨这些变化与基质水肿持续时间或 BK 的潜在病因的关系。

方法

对 6 个正常人和 16 个 BK 角膜进行二次谐波产生(SHG)成像显微镜检查,以允许胶原板层的三维(3-D)重建。通过免疫荧光分析和传统激光共聚焦显微镜检查,检测α-平滑肌肌动蛋白(αSMA)的表达。

结果

胶原板层在前基质中交织,在后基质中均匀排列,而正常角膜的整个基质中均未检测到αSMA。16 个 BK 角膜中有 9 个(56%)在前基质和 7 个(44%)在后基质中显示异常胶原结构。在 16 个 BK 角膜中,分别有 7 个(44%)和 6 个(38%)在前或后基质中检测到αSMA 的表达。只有在基质水肿持续时间至少 12 个月的角膜中才检测到胶原板层的紊乱和肌成纤维细胞的转分化。由出生损伤引起的 BK 的角膜显示后基质异常胶原结构,而由激光虹膜切开术引起的 BK 的角膜则没有。

结论

在基质水肿持续时间至少 12 个月的 BK 角膜中检测到整个基质结构的变化,表明这些变化可能是进展性的。此外,BK 的潜在病因可能会影响后基质的结构变化。

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