Multilayered Trabecular Meshwork for Dynamic In Vitro Studies in Glaucoma Research.

Magdalena Z Gładysz, Micaela Gaspar Gonçalves Fernandes, Xiaopeng Li, Marcus Koch, Frendion Marchena, Anno Hofman, Mariska de Graaf, Justina Clarinda Wolters, Marleen Kamperman, Anika Nagelkerke, Małgorzata K Włodarczyk-Biegun
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Abstract

Glaucoma, an eye disease causing incremental vision loss, currently has no cure. Its primary cause is the malfunction of the trabecular meshwork (TM), a multilayered tissue in the eye responsible for draining aqueous humor (AH) from the anterior chamber. TM clogging increases outflow resistance, elevates intraocular pressure (IOP), and damages optic nerves, leading to irreversible blindness. Existing in vitro TM models are suboptimal, as they lack the hierarchical structure of the TM. This article introduces a dynamic in vitro TM model, featuring a multilayered scaffold architecture 3D printed via melt electrowriting (MEW), and integrated with a flow system that enables continuous pressure monitoring during perfusion at native flow rates. Printed scaffolds supported the growth of primary adult human TM cells that grew on top and between the fibers. Cellularized scaffolds were tested under static and dynamic conditions. Over 3-5 days, pressure monitoring showed increased outflow resistance due to cell proliferation. Proteomic analysis revealed distinct changes in protein expression related to protein synthesis and respiration of cells grown under flow. Lat-B administration resulted in decreased pressure values and depolymerized actin filaments. These findings suggest that the proposed model is a promising alternative for in vitro glaucoma drug testing. STATEMENT OF SIGNIFICANCE: This study introduces a model of the trabecular meshwork (TM), a tissue in the eye involved in glaucoma, a common eye disease that currently has no cure. Using 3D printing, we created a multilayered scaffold that mimics the structure and function of the human TM. This allows us to study how cells behave and how drugs work under realistic conditions. Unlike existing models, ours accurately replicates all three layers of the TM, providing an advanced dynamic platform for glaucoma research. This innovation could help develop new treatments by offering a more reliable model for testing drugs and understanding how glaucoma works, making a significant impact on eye research.

青光眼动态体外多层小梁网研究。
青光眼是一种导致视力逐渐丧失的眼病,目前尚无治愈方法。其主要原因是小梁网(TM)的功能障碍,小梁网是眼内负责从前房排出房水(AH)的多层组织。TM堵塞增加流出阻力,升高眼压(IOP),损害视神经,导致不可逆失明。现有的体外TM模型是次优的,因为它们缺乏TM的层次结构。本文介绍了一种动态体外TM模型,该模型具有多层支架结构,通过熔融电解(MEW) 3D打印,并集成了一个流动系统,可以在灌注过程中以自然流速连续监测压力。打印支架支持生长在纤维顶部和纤维之间的原代成人TM细胞的生长。细胞化支架在静态和动态条件下进行了测试。3-5天的压力监测显示,由于细胞增殖,流出阻力增加。蛋白质组学分析显示,在流动条件下生长的细胞中,与蛋白质合成和呼吸有关的蛋白质表达发生了明显变化。给药后,压力值降低,肌动蛋白丝解聚。这些发现表明,所提出的模型是体外青光眼药物测试的一个有希望的替代方案。意义声明:本研究介绍了一种小梁网(TM)模型,这是一种与青光眼有关的眼部组织,青光眼是一种目前无法治愈的常见眼病。使用3D打印技术,我们创建了一个多层支架,模仿人类TM的结构和功能。这使我们能够研究细胞的行为和药物在现实条件下的作用。与现有模型不同,我们的模型准确地复制了TM的所有三层,为青光眼研究提供了一个先进的动态平台。这一创新可以通过提供一个更可靠的模型来测试药物和了解青光眼的工作原理,从而帮助开发新的治疗方法,对眼科研究产生重大影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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