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人组织工程角膜(hTEC):最新进展。

The Human Tissue-Engineered Cornea (hTEC): Recent Progress.

机构信息

CUO-Recherche, Médecine Régénératrice-Centre de Recherche du CHU de Québec, Université Laval, Québec, QC G1S 4L8, Canada.

Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, Québec, QC G1J 1Z4, Canada.

出版信息

Int J Mol Sci. 2021 Jan 28;22(3):1291. doi: 10.3390/ijms22031291.

Abstract

Each day, about 2000 U.S. workers have a job-related eye injury requiring medical treatment. Corneal diseases are the fifth cause of blindness worldwide. Most of these diseases can be cured using one form or another of corneal transplantation, which is the most successful transplantation in humans. In 2012, it was estimated that 12.7 million people were waiting for a corneal transplantation worldwide. Unfortunately, only 1 in 70 patients received a corneal graft that same year. In order to provide alternatives to the shortage of graftable corneas, considerable progress has been achieved in the development of living corneal substitutes produced by tissue engineering and designed to mimic their in vivo counterpart in terms of cell phenotype and tissue architecture. Most of these substitutes use synthetic biomaterials combined with immortalized cells, which makes them dissimilar from the native cornea. However, studies have emerged that describe the production of tridimensional (3D) tissue-engineered corneas using untransformed human corneal epithelial cells grown on a totally natural stroma synthesized by living corneal fibroblasts, that also show appropriate histology and expression of both extracellular matrix (ECM) components and integrins. This review highlights contributions from laboratories working on the production of human tissue-engineered corneas (hTECs) as future substitutes for grafting purposes. It overviews alternative models to the grafting of cadaveric corneas where cell organization is provided by the substrate, and then focuses on their 3D counterparts that are closer to the native human corneal architecture because of their tissue development and cell arrangement properties. These completely biological hTECs are therefore very promising as models that may help understand many aspects of the molecular and cellular mechanistic response of the cornea toward different types of diseases or wounds, as well as assist in the development of novel drugs that might be promising for therapeutic purposes.

摘要

每天,约有 2000 名美国工人因工作相关的眼部受伤需要接受治疗。角膜疾病是全球第五大致盲原因。这些疾病中的大多数可以通过角膜移植的一种或另一种形式治愈,这是人类最成功的移植形式。据估计,2012 年全球有 1270 万人在等待角膜移植。不幸的是,同年只有 1/70 的患者接受了角膜移植。为了提供对可移植角膜短缺的替代方案,在组织工程开发具有生物活性的角膜替代物方面取得了相当大的进展,这些替代物旨在在细胞表型和组织架构方面模拟其体内对应物。这些替代品中的大多数使用合成生物材料与永生化细胞结合,这使得它们与天然角膜不同。然而,已经出现了一些研究描述了使用未转化的人角膜上皮细胞在由活体角膜成纤维细胞合成的完全天然基质上生长,以制造三维(3D)组织工程角膜,该基质也表现出适当的组织学和细胞外基质(ECM)成分和整合素的表达。本综述重点介绍了致力于生产人组织工程角膜(hTEC)的实验室的贡献,hTEC 是作为移植替代物的未来替代品。它概述了替代尸体角膜移植的模型,其中细胞组织由基质提供,然后专注于它们的 3D 对应物,这些对应物更接近天然人角膜结构,因为它们具有组织发育和细胞排列特性。这些完全基于生物的 hTEC 作为模型非常有前途,因为它们可能有助于了解角膜对不同类型疾病或创伤的分子和细胞机制反应的许多方面,并有助于开发可能具有治疗潜力的新型药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aee3/7865732/cb9fbcd29eca/ijms-22-01291-g001.jpg

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