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通过超分子水凝胶工程开发全合成角膜基质构建体。

Development of a Fully Synthetic Corneal Stromal Construct via Supramolecular Hydrogel Engineering.

机构信息

Institute for Complex Molecular Systems, Department of Biomedical Engineering, Laboratory of Cell and Tissue Engineering, Laboratory of Chemical Biology, Eindhoven University of Technology, Groene Loper 7, Eindhoven, 5612 AZ, The Netherlands.

出版信息

Adv Healthc Mater. 2023 Dec;12(32):e2301392. doi: 10.1002/adhm.202301392. Epub 2023 Oct 5.

DOI:10.1002/adhm.202301392
PMID:37747759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11468521/
Abstract

Recent advances in the field of ophthalmology show great potential in the design of bioengineered constructs to mimic the corneal stroma. Hydrogels based on synthetic supramolecular polymers, are attractive synthetic mimics of the natural highly hydrated corneal stroma. Here, a fully synthetic corneal stromal construct is developed via engineering of an injectable supramolecular hydrogel based on ureido-pyrimidinone (UPy) moieties. The hydrogel displays a dynamic and tunable behavior, which allows for control of biochemical and mechanical cues. Two hydrogels are developed, a fully synthetic hydrogel functionalized with a bioactive cyclic arginine-glycine-aspartate UPy (UPy-cRGD) additive, and a hybrid hydrogel based on UPy-moieties mixed with collagen type I fibers. Both hydrogels supported cell encapsulation and associated cellular deposition of extracellular matrix (ECM) proteins after 21 days. Excitingly, the hydrogels support the activation of isolated primary keratocytes into stromal fibroblasts as well as the differentiation toward more quiescent corneal stromal keratocytes, demonstrated by their characteristic long dendritic protrusions and a substantially diminished cytokine secretion. Furthermore, cells survive shear stresses during an injectability test. Together, these findings highlight the development of an injectable supramolecular hydrogel as a synthetic corneal stromal microenvironment able to host primary keratocytes.

摘要

最近在眼科领域的进展表明,在设计仿生构建体以模拟角膜基质方面具有很大的潜力。基于合成超分子聚合物的水凝胶是天然高度水合角膜基质的有吸引力的合成模拟物。在这里,通过基于尿嘧啶嘧啶酮 (UPy) 部分的可注射超分子水凝胶的工程,开发了一种完全合成的角膜基质构建体。该水凝胶具有动态和可调谐的行为,可控制生化和机械线索。开发了两种水凝胶,一种是用生物活性环状精氨酸-甘氨酸-天冬氨酸 UPy (UPy-cRGD) 添加剂功能化的全合成水凝胶,另一种是基于 UPy 部分与 I 型胶原纤维混合的混合水凝胶。两种水凝胶均支持细胞包封,并在 21 天后细胞外基质 (ECM) 蛋白的相关细胞沉积。令人兴奋的是,水凝胶支持分离的原代角膜细胞向基质成纤维细胞的激活,以及向更静止的角膜基质角膜细胞的分化,这通过它们的特征性长树突状突起和明显减少的细胞因子分泌来证明。此外,细胞在可注射性测试期间能够承受剪切力。总之,这些发现强调了可注射超分子水凝胶作为能够容纳原代角膜细胞的合成角膜基质微环境的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/d6c4d4884ae2/ADHM-12-2301392-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/7c63f8a84500/ADHM-12-2301392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/6cbef443a3cc/ADHM-12-2301392-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/1e808f4e93e7/ADHM-12-2301392-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/146c719bc4f4/ADHM-12-2301392-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/1bc88c1a8f45/ADHM-12-2301392-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/81fafad17679/ADHM-12-2301392-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/d6c4d4884ae2/ADHM-12-2301392-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/7c63f8a84500/ADHM-12-2301392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/6cbef443a3cc/ADHM-12-2301392-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/1e808f4e93e7/ADHM-12-2301392-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/146c719bc4f4/ADHM-12-2301392-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/1bc88c1a8f45/ADHM-12-2301392-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/81fafad17679/ADHM-12-2301392-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5525/11468521/d6c4d4884ae2/ADHM-12-2301392-g004.jpg

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