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具有单轴排列孔隙的胶原蛋白和胶原蛋白-硫酸软骨素支架,用于小梁网细胞的仿生三维培养。

Collagen and collagen-chondroitin sulfate scaffolds with uniaxially aligned pores for the biomimetic, three dimensional culture of trabecular meshwork cells.

作者信息

Osmond Matthew, Bernier Sarah M, Pantcheva Mina B, Krebs Melissa D

机构信息

Department of Chemical and Biological Engineering, Colorado School of Mines, 1613 Illinois Street, 431 Alderson Hall, Golden, 80401, Colorado.

Department of Ophthalmology, University of Colorado Denver, 1675 Aurora Court, Aurora, 80045, Colorado.

出版信息

Biotechnol Bioeng. 2017 Apr;114(4):915-923. doi: 10.1002/bit.26206. Epub 2016 Nov 7.

Abstract

Glaucoma is a disease in which damage to the optic nerve leads to progressive, irreversible vision loss. The intraocular pressure (IOP) is the only modifiable risk factor for glaucoma and its lowering is considered a useful strategy for preventing or slowing down the progression of glaucomatous neuropathy. Elevated intraocular pressure associated with glaucoma is due to increased aqueous humor outflow resistance, primarily through the trabecular meshwork (TM) of the eye. Current in vitro models of the trabecular meshwork are oversimplified and do not capture the organized and complex three-dimensional nature of this tissue that consists primarily of collagen and glycoasaminoglycans. In this work, collagen and collagen-chondroitin sulfate (CS) scaffolds were fabricated via unidirectional freezing and lyophilization to induce the formation of aligned pores. Scaffolds were characterized by scanning electron microscopy, dynamic mechanical analysis, and a chondroitin sulfate quantification assay. Scaffold characterization confirmed the formation of aligned pores, and also that the CS was leaching out of the scaffolds over time. Primary porcine trabecular meshwork (TM) cells were seeded onto the surface of scaffolds and their gene expression, proliferation, viability, migration into the scaffolds, and morphology were examined. The TM cells were viable and proliferated 2 weeks after seeding. The cells migrated down into the internal scaffold structure and their morphology reflected the topography and alignment of the scaffold structure. This work is a promising step toward the development of a three dimensional in vitro model of the TM that can be used for testing of glaucoma pharmacological agents in future experimentation and to better our understanding of the trabecular meshwork and its complex physiology. Biotechnol. Bioeng. 2017;114: 915-923. © 2016 Wiley Periodicals, Inc.

摘要

青光眼是一种因视神经受损而导致渐进性、不可逆视力丧失的疾病。眼内压(IOP)是青光眼唯一可改变的危险因素,降低眼内压被认为是预防或减缓青光眼性神经病变进展的有效策略。与青光眼相关的眼内压升高是由于房水流出阻力增加,主要是通过眼睛的小梁网(TM)。目前小梁网的体外模型过于简化,无法捕捉该组织主要由胶原蛋白和糖胺聚糖组成的有组织且复杂的三维特性。在这项研究中,通过单向冷冻和冻干制备了胶原蛋白和胶原蛋白 - 硫酸软骨素(CS)支架,以诱导形成排列有序的孔。通过扫描电子显微镜、动态力学分析和硫酸软骨素定量测定对支架进行了表征。支架表征证实了排列有序的孔的形成,并且随着时间的推移,CS从支架中渗出。将原代猪小梁网(TM)细胞接种到支架表面,并检测其基因表达、增殖、活力、向支架内的迁移以及形态。接种后2周,TM细胞存活并增殖。细胞向下迁移到支架内部结构中,其形态反映了支架结构的地形和排列。这项工作朝着开发一种TM的三维体外模型迈出了有希望的一步,该模型可用于未来实验中青光眼药物的测试,并增进我们对小梁网及其复杂生理学的理解。《生物技术与生物工程》2017年;114:915 - 923。©2016威利期刊公司

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