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器官培养的人角膜上皮和内皮的完整性。

Integrity of epithelium and endothelium in organ-cultured human corneas.

作者信息

Crewe J M, Armitage W J

机构信息

Division of Ophthalmology, University of Bristol, Bristol Eye Hospital, Lower Maudlin Street, Bristol BS1 2LX, United Kingdom.

出版信息

Invest Ophthalmol Vis Sci. 2001 Jul;42(8):1757-61.

Abstract

PURPOSE

To examine components of the junctional complex and the actin cytoskeleton and the incidence of apoptosis in epithelium and endothelium of organ-cultured human corneas.

METHODS

Human corneas, either organ-cultured for 1 to >28 days or excised directly from eyes stored in moist chambers, were stained with antibodies to ZO-1, vinculin, and caspase 3 coupled to FITC-conjugated secondary antibody. These markers were combined with rhodamine-phalloidin staining for F-actin and DAPI labeling for DNA. The corneas were examined by confocal microscopy.

RESULTS

The depth of the epithelium was reduced during organ culture, but no changes were observed in the distribution of ZO-1 or vinculin, or in the F-actin cytoskeleton. The appearance of apoptotic epithelial cells positive for caspase 3 or with condensed DNA increased with time after 14 days in organ culture, but there was no correlation with donor age. ZO-1 and F-actin staining patterns in endothelium were similarly undisturbed by organ culture, but apoptotic endothelial cells were only rarely seen and then only after >28 days in organ culture.

CONCLUSIONS

Organ culture maintained the integrity of tight junctions and the actin cytoskeleton in epithelial and endothelial cell layers. Apoptosis was evident in epithelium but was observed rarely in the endothelium and then only after extended periods in organ culture.

摘要

目的

研究器官培养的人角膜上皮和内皮中连接复合体、肌动蛋白细胞骨架的组成成分以及细胞凋亡的发生率。

方法

将器官培养1至超过28天的人角膜或直接从保存在湿盒中的眼中取出的角膜,用与异硫氰酸荧光素(FITC)偶联的二抗结合的抗紧密连接蛋白1(ZO-1)、纽蛋白和半胱天冬酶3抗体进行染色。这些标志物与用于F-肌动蛋白的罗丹明-鬼笔环肽染色以及用于DNA的4',6-二脒基-2-苯基吲哚(DAPI)标记相结合。通过共聚焦显微镜检查角膜。

结果

在器官培养期间上皮层深度降低,但ZO-1或纽蛋白的分布以及F-肌动蛋白细胞骨架未观察到变化。在器官培养14天后,半胱天冬酶3阳性或DNA浓缩的凋亡上皮细胞的出现随时间增加,但与供体年龄无关。器官培养对内皮中的ZO-1和F-肌动蛋白染色模式同样没有干扰,但凋亡内皮细胞很少见,且仅在器官培养超过28天后出现。

结论

器官培养维持了上皮和内皮细胞层中紧密连接和肌动蛋白细胞骨架的完整性。细胞凋亡在上皮层明显,但在内皮层很少见,且仅在器官培养较长时间后才观察到。

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