首页> 外文期刊>Histology and histopathology >Impairment of thrombospondin-1 expression during epithelial wound healing in corneas of vitamin A-deficient mice.
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Impairment of thrombospondin-1 expression during epithelial wound healing in corneas of vitamin A-deficient mice.

机译:维生素A缺乏症小鼠角膜上皮伤口愈合期间血小板反应蛋白1的表达受损。

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The purpose of this study is to investigate the expression of thrombospondin-1 (TSP-1), a multifunctional extracellular matrix protein, during re-epithelialization in wounded corneas of vitamin A-deficient mice. Epithelial defects were created in the corneas of normal and Vitamin A-deficient mice with a microgrinder. Wounded corneas were stained with fluorescein and photographed for evaluation of re-epithelialization. Histological examination and immunohistochemical analysis of TSP-1 expression were also performed on the specimens from wounded corneas. In vitamin A-deficient mice, re-epithelialization of the wounded corneal epithelium was significantly delayed compared with that in normal mice. TSP-1 was detectable neither in the unwounded corneal epithelium of normal mice nor in that of vitamin A-deficient mice. In normal mice, linear staining of TSP-1 was observed on the wounded corneal surface and stroma at 30 min and 8 h to 16 h, respectively, after abrasion, and this TSP-1 expression disappeared at 36 to 48 h, when re-epithelialization was completed. In contrast, no TSP-1 staining was observed in the wounded corneas of vitamin A-deficient mice, except for the endothelial cells, throughout the wound healing process. Histological examination revealed a progressive increase in polymorphonuclear neutrophil infiltration in the stroma of the corneas of vitamin A-deficient mice during the healing process. These findings suggest that vitamin A may modulate the expression of TSP-1 in the corneas to accelerate the re-epithelialization of wounded corneas.
机译:这项研究的目的是调查在维生素A缺乏症小鼠的受伤角膜上皮再形成过程中,血小板反应蛋白1(TSP-1)(一种多功能的细胞外基质蛋白)的表达。带有微研磨器的正常小鼠和维生素A缺乏症小鼠的角膜中产生了上皮缺损。用荧光素对受伤的角膜染色,并照相以评估再上皮形成。还对受伤角膜的标本进行了TSP-1表达的组织学检查和免疫组化分析。与正常小鼠相比,在缺乏维生素A的小鼠中,受伤的角膜上皮的重新上皮形成明显延迟。在正常小鼠未受伤的角膜上皮和缺乏维生素A的小鼠中均未检测到TSP-1。在正常小鼠中,磨损后分别在30分钟和8h至16h时,在受伤的角膜表面和间质上观察到TSP-1的线性染色,而当再灌注时,TSP-1的表达在36至48h消失。上皮化完成。相反,在整个伤口愈合过程中,除了内皮细胞外,在缺乏维生素A的小鼠的受伤角膜中未观察到TSP-1染色。组织学检查显示,在愈合过程中,维生素A缺乏症小鼠角膜基质中的多形核中性粒细胞浸润逐渐增加。这些发现表明,维生素A可调节角膜中TSP-1的表达,从而加速受伤角膜的上皮再生。

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