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假性剥脱综合征中含原纤维蛋白的纤维在细胞外的沉积增加。

Increased extracellular deposition of fibrillin-containing fibrils in pseudoexfoliation syndrome.

作者信息

Schlötzer-Schrehardt U, von der Mark K, Sakai L Y, Naumann G O

机构信息

Department of Ophthalmology, University of Erlangen-Nürnberg, Germany.

出版信息

Invest Ophthalmol Vis Sci. 1997 Apr;38(5):970-84.

PMID:9112993
Abstract

PURPOSE

To localize the distribution of fibrillin-containing microfibrils in normal human anterior segment tissues and to characterize the role of fibrillin in the pathogenesis of pseudoexfoliation syndrome.

METHODS

Anterior segment tissues were obtained from 10 eyes with pseudoexfoliation syndrome and 10 normal eyes and investigated by indirect immunofluorescence and electron microscopic immunogold labeling using a monoclonal antibody to fibrillin-1.

RESULTS

In addition to labeling of zonular fibers, fibrillin-immunoreactive microfibrillar bundles generally were found in the corneal stroma; the stromal connective tissues of conjunctiva, ciliary body, and iris, especially in the iris root area; the periphery of Schlemm's canal, the scleral spur, and the most anterior portion of the trabecular meshwork; the ciliary muscle, and the dilator and sphincter muscles of the iris; the basement membranes of peripheral corneal epithelium, conjunctival epithelium, ciliary pigmented epithelium, and the lens capsule. The microfibrillar bundles were found to be isolated or in association with elastic fibers and cellular basement membranes. In pseudoexfoliation eyes, an additional strong immunoreaction was localized to pseudoexfoliation fibers and their microfibrillar subunits in close proximity to surfaces of cells involved in pseudoexfoliation fiber production.

CONCLUSIONS

The fibrillin-containing microfibrillar system in normal ocular tissues is suggested to have a substantial role in the maintenance of tissue integrity by providing tensile strength and flexibility to mechanically strained tissues. The findings further provide evidence for fibrillin as an intrinsic component of pseudoexfoliation fibers, suggesting the possibility that enhanced expression of fibrillin or abnormal aggregation of fibrillin-containing microfibrils may be involved in the pathogenesis of pseudoexfoliation syndrome.

摘要

目的

定位正常人眼前节组织中含原纤维蛋白的微原纤维的分布,并阐明原纤维蛋白在假性剥脱综合征发病机制中的作用。

方法

从10只患有假性剥脱综合征的眼睛和10只正常眼睛获取眼前节组织,使用抗原纤维蛋白-1单克隆抗体,通过间接免疫荧光和电子显微镜免疫金标记进行研究。

结果

除了标记悬韧带纤维外,原纤维蛋白免疫反应性微原纤维束通常见于角膜基质;结膜、睫状体和虹膜的基质结缔组织,尤其是虹膜根部区域;施莱姆管周边、巩膜突和小梁网最前部;睫状肌以及虹膜的瞳孔开大肌和瞳孔括约肌;周边角膜上皮、结膜上皮、睫状体色素上皮和晶状体囊膜的基底膜。发现微原纤维束是孤立的,或与弹性纤维和细胞基底膜相关。在假性剥脱眼中,另一个强免疫反应定位于假性剥脱纤维及其微原纤维亚单位,紧邻参与假性剥脱纤维产生的细胞表面。

结论

正常眼组织中含原纤维蛋白的微原纤维系统通过为机械应变组织提供抗张强度和柔韧性,在维持组织完整性方面发挥重要作用。这些发现进一步为原纤维蛋白作为假性剥脱纤维的内在成分提供了证据,提示原纤维蛋白表达增强或含原纤维蛋白的微原纤维异常聚集可能参与假性剥脱综合征发病机制的可能性。

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