利用人体角膜细胞系构建具有神经支配功能的体外三维胶原蛋白角膜结构

IF 3.2 Q1 OPHTHALMOLOGY
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引用次数: 0

摘要

设计使用化学交联的胶原蛋白和硫酸软骨素细胞外基质创建了体外人类角膜构建体,并将 3 种人类角膜细胞类型(上皮细胞、基质细胞和内皮细胞)与神经细胞一起播种到构建体中。神经细胞来自杂交神经母细胞瘤细胞,其他细胞来自永生化人类角膜细胞系。为了检验构建物的可行性并确定其特征,对构建物进行了细胞毒性、细胞增殖、组织学和蛋白质表达研究。构建体显示出不同细胞层的典型外观,包括健康外观、表型分化的神经元。结论 成功开发了一种体外角膜构建体,其细胞表型保持了解剖学上正确的细胞位置。该构建体可能有助于评估特定的角膜疾病和开发不同的角膜疾病模型。此外,该构建体还可用于评估药物的靶向性和/或对单个角膜层的渗透性,测试角膜疾病的新型疗法,并有可能在研究的早期阶段减少角膜研究中使用动物的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An in vitro 3-dimensional Collagen-based Corneal Construct with Innervation Using Human Corneal Cell Lines

Purpose

To develop a 3-dimensional corneal construct suitable for in vitro studies of disease conditions and therapies.

Design

In vitro human corneal constructs were created using chemically crosslinked collagen and chondroitin sulfate extracellular matrix and seeded with 3 human corneal cell types (epithelial, stromal, and endothelial) together with neural cells. The neural cells were derived from hybrid neuroblastoma cells and the other cells used from immortalized human corneal cell lines. To check the feasibility and characterize the constructs, cytotoxicity, cell proliferation, histology, and protein expression studies were performed.

Results

Optimized culture condition permitted synchronized viability across the cell types within the construct. The construct showed a typical appearance for different cellular layers, including healthy appearing, phenotypically differentiated neurons. The expected protein expression profiles for specific cell types within the construct were confirmed with western blotting.

Conclusions

An in vitro corneal construct was successfully developed with maintenance of individual cell phenotypes with anatomically correct cellular loci. The construct may be useful in evaluation of specific corneal disorders and in developing different corneal disease models. Additionally, the construct can be used in evaluating drug targeting and/or penetration to individual corneal layers, testing novel therapeutics for corneal diseases, and potentially reducing the necessity for animals in corneal research at the early stages of investigation.

Financial Disclosure(s)

Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

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来源期刊
Ophthalmology science
Ophthalmology science Ophthalmology
CiteScore
3.40
自引率
0.00%
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审稿时长
89 days
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