三维人体角膜组织模型的组装与应用

Q3 Pharmacology, Toxicology and Pharmaceutics
Tina B McKay, Andrew Ford, Siran Wang, Dana M. Cairns, Rachael N. Parker, Phillip M. Deardorff, C. Ghezzi, D. Kaplan
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引用次数: 9

摘要

角膜提供了将外部环境与眼内环境分离的功能屏障,从而保护眼睛后部免受感染和损伤。损伤或疾病可能会导致损害角膜结构或完整性的病理变化,并可能导致视力下降。全世界有1000多万人因角膜混浊而视力受损或失明。因此,需要采用生理相关的体外方法来预测化学物质的角膜毒性或在眼睛暴露前对疾病的有效治疗,以及研究全身慢性疾病(如糖尿病)的角膜影响,以减少动物试验的使用并加速治疗发展。我们之前已经使用丝蛋白支架对神经支配的角膜组织模型进行了生物工程,以概括前角膜的结构和机械元件,并通过包括上皮、基质和神经成分来对角膜感觉的功能方面进行建模。本单元的目的是为这种三维角膜组织系统的制备、组装和应用提供一个循序渐进的指南,以实现角膜组织生物学的研究。©2019 John Wiley&Sons,股份有限公司版权所有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assembly and Application of a Three‐Dimensional Human Corneal Tissue Model
The cornea provides a functional barrier separating the outside environment from the intraocular environment, thereby protecting posterior segments of the eye from infection and damage. Pathological changes that compromise the structure or integrity of the cornea may occur as a result of injury or disease and can lead to debilitating effects on visual acuity. Over 10 million people worldwide are visually impaired or blind due to corneal opacity. Thus, physiologically relevant in vitro approaches to predict corneal toxicity of chemicals or effective treatments for disease prior to ocular exposure, as well as to study the corneal effects of systemic, chronic conditions, such as diabetes, are needed to reduce use of animal testing and accelerate therapeutic development. We have previously bioengineered an innervated corneal tissue model using silk protein scaffolds to recapitulate the structural and mechanical elements of the anterior cornea and to model the functional aspects of corneal sensation with the inclusion of epithelial, stromal, and neural components. The purpose of this unit is to provide a step‐by‐step guide for preparation, assembly, and application of this three‐dimensional corneal tissue system to enable the study of corneal tissue biology. © 2019 by John Wiley & Sons, Inc.
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