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兔角膜上皮细胞在伤口修复过程中波形蛋白的表达。

Expression of vimentin by rabbit corneal epithelial cells during wound repair.

作者信息

SundarRaj N, Rizzo J D, Anderson S C, Gesiotto J P

机构信息

Department of Ophthalmology, Eye Ear Institute, Pittsburgh, PA.

出版信息

Cell Tissue Res. 1992 Feb;267(2):347-56. doi: 10.1007/BF00302973.

Abstract

Intermediate filaments of epithelial cells generally consist of specific combinations of keratins. However, cultured epithelial cells from certain tissues and some epithelial tumors have been shown also to express vimentin. In the present study, the expression of vimentin by epithelial cells in healing corneal wounds (partial thickness penetrating wounds) and in tissue culture was analyzed. Both immunohistochemical and immunotransblot analyses indicated that although vimentin was not detected in the normal rabbit corneal epithelium in vivo, cultured rabbit corneal epithelial cells co-express keratins and vimentin. At 1 day post-wounding, vimentin was not detectable in the epithelial cells that had covered the denuded stroma. However, at 2 days postwounding, the epithelium at the base of the epithelial plug immunoreacted with both anti-vimentin and antikeratin monoclonal antibodies. Immunotransblot analyses of the extracts of the epithelial plugs confirmed the presence of vimentin (Mr = 58k). The 58k band was not detected in the extract of normal rabbit corneal epithelium. At day/5, vimentin was no longer detectable in the epithelium. This study demonstrated that corneal epithelial cells transiently co-express vimentin and keratins in vivo during wound healing and in tissue culture. The time-course of the transient expression of vimentin suggests that the vimentin expression in the epithelial cells during healing is not linked to cell proliferation or to the centripetal migration of the epithelium during early stages (first 24 h) of healing, but may be linked to cell-matrix interactions or the migration of basal cells in the upward direction at the following stage of healing.

摘要

上皮细胞的中间丝通常由特定组合的角蛋白构成。然而,已证实来自某些组织的培养上皮细胞以及一些上皮肿瘤也表达波形蛋白。在本研究中,分析了愈合角膜伤口(部分厚度穿透性伤口)和组织培养中上皮细胞波形蛋白的表达情况。免疫组织化学和免疫印迹分析均表明,尽管在正常兔角膜上皮的体内未检测到波形蛋白,但培养的兔角膜上皮细胞同时表达角蛋白和波形蛋白。受伤后1天,覆盖裸露基质的上皮细胞中未检测到波形蛋白。然而,受伤后2天,上皮栓底部的上皮与抗波形蛋白和抗角蛋白单克隆抗体均发生免疫反应。上皮栓提取物的免疫印迹分析证实了波形蛋白(分子量=58k)的存在。在正常兔角膜上皮提取物中未检测到58k条带。在第5天,上皮中不再能检测到波形蛋白。本研究表明,角膜上皮细胞在伤口愈合过程中及组织培养时在体内短暂地同时表达波形蛋白和角蛋白。波形蛋白短暂表达的时间进程表明,愈合过程中上皮细胞中波形蛋白的表达与细胞增殖或愈合早期(最初24小时)上皮的向心迁移无关,但可能与细胞-基质相互作用或愈合后续阶段基底细胞向上迁移有关。

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