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角膜小切口术后粘连复合体的形成。

Adhesion complex formation after small keratectomy wounds in the cornea.

作者信息

Stock E L, Kurpakus M A, Sambol B, Jones J C

机构信息

Cornea and External Eye Disease Laboratory, VA Lakeside Medical Center, Chicago, Illinois.

出版信息

Invest Ophthalmol Vis Sci. 1992 Feb;33(2):304-13.

PMID:1740360
Abstract

The adhesion complex of the corneal epithelium consists of the hemidesmosome and its associated structures, such as anchoring filaments, lamina densa of the basement membrane, and anchoring fibrils. It contributes to the adhesion of the corneal epithelium to Bowman's layer. To understand the adhesion complex better, an electron microscopic and immunofluorescence analysis was done of the reformation of the adhesion complex in small (1 mm) keratectomy wounds in the guinea pig cornea. In these wounds, the epithelium, hemidesmosomes, basal lamina, anchoring fibrils, and anterior stroma were removed. The wound bed was epithelialized completely by 24 hr after wounding. Immunofluorescence analyses involved the use of antibodies against plaque components of the hemidesmosome, an antibody against laminin, and an antibody against the collagen VII component of anchoring fibrils. At 18 hr after wounding, there was no morphologic evidence of hemidesmosomes at the epithelial-stromal interface. At 24 hr, hemidesmosomes were observed, with or without subjacent lamina densa. Furthermore, plaque components were detected by immunofluorescence in those cells in contact with the wound bed. In contrast, no type VII collagen was detected. On day 7, collagen VII, laminin, and bullous pemphigoid autoantibody markers colocalized along the wound bed as determined by immunofluorescence. However, at the ultrastructural level, even though the lamina densa of the basal lamina was observed primarily where hemidesmosomes were present, it remained incomplete. In this study, the precise temporal sequence in which components are incorporated into the assembling adhesion complex was described during wound healing. Furthermore, the possibility that the hemidesmosomal plaque nucleates the formation of the underlying basal lamina was discussed.

摘要

角膜上皮的黏附复合体由半桥粒及其相关结构组成,如锚定丝、基底膜的致密层和锚定原纤维。它有助于角膜上皮与Bowman层的黏附。为了更好地理解黏附复合体,对豚鼠角膜小(1毫米)角膜切除术伤口中黏附复合体的重塑进行了电子显微镜和免疫荧光分析。在这些伤口中,上皮、半桥粒、基底膜、锚定原纤维和前部基质被去除。伤口在受伤后24小时完全被上皮化。免疫荧光分析使用了针对半桥粒斑块成分的抗体、针对层粘连蛋白的抗体和针对锚定原纤维的胶原VII成分的抗体。在受伤后18小时,上皮-基质界面处没有半桥粒的形态学证据。在24小时时,观察到了半桥粒,有或没有下方的致密层。此外,通过免疫荧光在与伤口床接触的那些细胞中检测到了斑块成分。相比之下,未检测到VII型胶原。在第7天,通过免疫荧光确定,胶原VII、层粘连蛋白和大疱性类天疱疮自身抗体标记物沿伤口床共定位。然而,在超微结构水平上,即使主要在存在半桥粒的地方观察到基底膜的致密层,但它仍然不完整。在本研究中,描述了伤口愈合过程中各成分整合到正在组装的黏附复合体中的精确时间顺序。此外,还讨论了半桥粒斑块使下方基底膜形成成核的可能性。

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