Uno K, Kuroki M, Hayashi H, Uchida H, Kuroki M, Oshima K
Department of Ophthalmology, Fukuoka University School of Medicine, Fukuoka, Japan.
Histol Histopathol. 2005 Apr;20(2):493-9. doi: 10.14670/HH-20.493.
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.
本研究的目的是调查多功能细胞外基质蛋白血小板反应蛋白-1(TSP-1)在维生素A缺乏小鼠角膜创伤后再上皮化过程中的表达。用微型研磨器在正常和维生素A缺乏小鼠的角膜上造成上皮缺损。用荧光素对创伤角膜进行染色并拍照,以评估再上皮化情况。还对创伤角膜标本进行了TSP-1表达的组织学检查和免疫组织化学分析。与正常小鼠相比,维生素A缺乏小鼠创伤角膜上皮的再上皮化明显延迟。在正常小鼠和维生素A缺乏小鼠未受伤的角膜上皮中均未检测到TSP-1。在正常小鼠中,擦伤后30分钟以及8小时至16小时,分别在创伤角膜表面和基质中观察到TSP-1的线性染色,当再上皮化完成时,这种TSP-1表达在36至48小时消失。相比之下,在整个伤口愈合过程中,除内皮细胞外,在维生素A缺乏小鼠的创伤角膜中未观察到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可能调节角膜中TSP-1的表达,以加速创伤角膜的再上皮化。