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虹膜缺失相关角膜病变:未受影响和移植角膜移植片的结构变化。

Aniridia-related keratopathy: Structural changes in naïve and transplanted corneal buttons.

机构信息

Department of Clinical Science, Ophthalmology, Umeå University, Umeå, Sweden.

Department of Integrative Medical Biology, Section for Anatomy, Umeå University, Umeå, Sweden.

出版信息

PLoS One. 2018 Jun 11;13(6):e0198822. doi: 10.1371/journal.pone.0198822. eCollection 2018.

Abstract

BACKGROUND

To study structural changes in naïve and surgically treated corneas of aniridia patients with advanced aniridia-related keratopathy (ARK).

METHODS AND FINDINGS

Two naïve corneal buttons from patients with advanced ARK submitted to penetrating keratoplasty for the first time, one corneal button from an ARK patient that had undergone a keratolimbal allograft (KLAL), two corneal buttons from ARK patients who had previously undergone centered or decentered transplantation and were now retransplanted and two adult healthy donor control corneas were processed for immunohistochemistry. Antibodies against extracellular matrix components in the stroma and in the epithelial basement membrane (collagen I and IV, collagen receptor α11 integrin and laminin α3 chain), markers of fibrosis, wound healing and vascularization (fibronectin, tenascin-C, vimentin, α-SMA and caveolin-1), cell division (Ki-67) and macrophages (CD68) were used. Naïve ARK, KLAL ARK corneas and transplanted corneal buttons presented similar histopathological changes with irregular epithelium and disruption or absence of epithelial basal membrane. There was a loss of the orderly pattern of collagen lamellae and absence of collagen I in all ARK corneas. Vascularization was revealed by the presence of caveolin-1 and collagen IV in the pannus of all ARK aniridia corneas. The changes observed in decentered and centered transplants were analogous.

CONCLUSIONS

Given the similar pathological features of all cases, conditions inherent to the host seem to play an important role on the pathophysiology of the ARK in the long run.

摘要

背景

研究未经处理和经手术治疗的伴有晚期虹膜角膜营养不良(ARK)的无虹膜患者的角膜的结构变化。

方法和发现

对首次接受穿透性角膜移植术的晚期 ARK 患者的 2 个未经处理的角膜瓣、1 个接受角膜缘干细胞移植术(KLAL)的 ARK 患者的角膜瓣、2 个先前接受过中心或偏心移植术、现再次移植的 ARK 患者的角膜瓣和 2 个成人健康供体对照角膜进行免疫组织化学处理。使用针对基质和上皮基底膜中的细胞外基质成分(胶原 I 和 IV、胶原受体α11 整合素和层粘连蛋白α3 链)、纤维化、伤口愈合和血管生成标志物(纤连蛋白、腱糖蛋白-C、波形蛋白、α-SMA 和窖蛋白-1)、细胞分裂(Ki-67)和巨噬细胞(CD68)的抗体。未经处理的 ARK、KLAL ARK 角膜和移植角膜瓣均表现出相似的组织病理学变化,表现为上皮不规则和上皮基底膜中断或缺失。所有 ARK 角膜均出现胶原板层有序模式丧失和胶原 I 缺失。所有 ARK 无虹膜角膜的血管生成通过 pannus 中存在窖蛋白-1 和胶原 IV 来揭示。偏心和中心移植的变化是类似的。

结论

鉴于所有病例的病理特征相似,宿主固有的条件似乎在长期内对 ARK 的病理生理学起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/098b/5995400/464b3594431d/pone.0198822.g001.jpg

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