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Fenótipos clínicos e anisotropias ópticas da córnea em coelhos com deficiência de células tronco limbais

机译:角膜缘干细胞缺乏症兔的临床表型和角膜光学各向异性

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Purposes: To investigate the intra-laboratory reproducibility of clinical features and to evaluate corneal optical anisotropies in a rabbit model of limbal stem cell deficiency. Methods: Limbal injury was induced in the right eye of 23 adult New Zealand White rabbits using a highly aggressive protocol that combined 360 degrees limbal peritomy, keratolimbectomy, alkaline chemical burn, and mechanical removal of the epithelium. Clinical evaluation of the injured eyes was performed for 28 days and included corneal impression cytology. Corneas with a severe clinical outcome set typical of limbal stem cell deficiency were then collected, subjected to a histopathological examination, and examined for optical anisotropies. Corneas from healthy rabbit eyes were used as controls. Differences in optical path due to stromal collagen birefringence, as well as linear dichroism related to the expression and spatial orientation of glycosaminoglycan chains from proteoglycans, were measured from cross-sections under a quantitative polarized light microscope. Results: One eye showed signs of hypopyon and was excluded. Signs of ocular inflammation were observed in all eyes studied (n=22). Corneal impression cytology did not detect goblet cells. Twelve of the 22 corneas presented a clinical outcome set typical of limbal stem cell deficiency, which is characterized by the presence of epithelial defects, inflammatory cells, moderate-to-severe opacity, and neovascularization. Microscopic studies under polarized light revealed that relative to controls, limbal stem cell deficiency caused a 24.4% increase in corneal optical path differences. Further, corneas with limbal stem cell deficiency were less dichroic than controls. Conclusions: These results suggest that rabbit models of limbal stem cell deficiency must be rigorously screened for use in preclinical studies to ensure experimental homogeneity because protocols used to create limbal stem cell deficiency could be not associated with good intra-laboratory reproducibility of clinical features. Limbal stem cell deficiency, as induced herein, altered the optical anisotropic properties of the corneal stroma. Such alterations are indicative of changes in collagen packing and the spatial orientation of glycosaminoglycan chains from proteoglycans. Knowledge of these changes is important to potentiate strategies aimed at restoring the morphofunctional integrity of the corneal stroma affected by limbal stem cell deficiency.
机译:目的:研究实验室特征在实验室中的再现性,并评估角膜缘光学各向异性在兔角膜缘干细胞缺乏症模型中的作用。方法:采用高度侵袭性的方案,将360度角膜缘周膜切开术,角膜缘缘切除术,碱性化学灼伤和机械去除上皮相结合,在23只成年新西兰白兔的右眼中引起肢体损伤。对受伤的眼睛进行了28天的临床评估,包括角膜印象细胞学检查。然后收集具有典型的角膜缘干细胞缺乏症的严重临床结局的角膜,进行组织病理学检查,并检查光学各向异性。来自健康兔子眼睛的角膜用作对照。在定量偏振光显微镜下,从横截面测量由于基质胶原双折射引起的光路差异以及与蛋白聚糖糖胺聚糖链的表达和空间取向有关的线性二向色性。结果:一只眼睛出现hyperpyon的迹象,被排除在外。在所有研究的眼睛中均观察到眼部炎症的迹象(n = 22)。角膜印模细胞学未检测到杯状细胞。 22个角膜中有12个呈现出典型的角膜缘干细胞缺乏症的临床结局,其特征是存在上皮缺损,炎性细胞,中度至重度不透明以及新血管形成。在偏振光下的显微镜研究表明,相对于对照,角膜缘干细胞缺乏导致角膜光程差增加24.4%。此外,角膜缘角膜缘干细胞缺乏症的二向色性低于对照组。结论:这些结果表明,必须严格筛选兔角膜缘干细胞缺乏症的模型以用于临床前研究,以确保实验的同质性,因为用于产生角膜缘干细胞缺乏症的方案可能与实验室内临床特征的良好再现性无关。如本文所诱导的,角膜干细胞缺乏改变了角膜基质的光学各向异性。这种改变表明胶原蛋白堆积的变化和来自蛋白聚糖的糖胺聚糖链的空间取向。了解这些变化对于增强旨在恢复受角膜缘干细胞缺乏症影响的角膜基质的形态功能完整性的策略至关重要。

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