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用于血管组织工程的具有生物指令性的层层涂覆的可定制 3D 打印可灌注微通道,嵌入光交联水凝胶中。

Bioinstructive Layer-by-Layer-Coated Customizable 3D Printed Perfusable Microchannels Embedded in Photocrosslinkable Hydrogels for Vascular Tissue Engineering.

机构信息

CICECO-Aveiro Institute of Materials, Department of Chemistry, University of Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.

出版信息

Biomolecules. 2021 Jun 10;11(6):863. doi: 10.3390/biom11060863.

DOI:10.3390/biom11060863
PMID:34200682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8230362/
Abstract

The development of complex and large 3D vascularized tissue constructs remains the major goal of tissue engineering and regenerative medicine (TERM). To date, several strategies have been proposed to build functional and perfusable vascular networks in 3D tissue-engineered constructs to ensure the long-term cell survival and the functionality of the assembled tissues after implantation. However, none of them have been entirely successful in attaining a fully functional vascular network. Herein, we report an alternative approach to bioengineer 3D vascularized constructs by embedding bioinstructive 3D multilayered microchannels, developed by combining 3D printing with the layer-by-layer (LbL) assembly technology, in photopolymerizable hydrogels. Alginate (ALG) was chosen as the ink to produce customizable 3D sacrificial microstructures owing to its biocompatibility and structural similarity to the extracellular matrices of native tissues. ALG structures were further LbL coated with bioinstructive chitosan and arginine-glycine-aspartic acid-coupled ALG multilayers, embedded in shear-thinning photocrosslinkable xanthan gum hydrogels and exposed to a calcium-chelating solution to form perfusable multilayered microchannels, mimicking the biological barriers, such as the basement membrane, in which the endothelial cells were seeded, denoting an enhanced cell adhesion. The 3D constructs hold great promise for engineering a wide array of large-scale 3D vascularized tissue constructs for modular TERM strategies.

摘要

构建复杂且大型的 3D 血管化组织构建体仍然是组织工程和再生医学 (TERM) 的主要目标。迄今为止,已经提出了几种策略来构建 3D 组织工程构建体中的功能性和可灌注血管网络,以确保植入后长期的细胞存活和组装组织的功能。然而,它们都没有完全成功地实现完全功能性的血管网络。在此,我们报告了一种通过将生物指令性 3D 多层微通道嵌入光聚合水凝胶中,来生物工程化 3D 血管化构建体的替代方法。由于其生物相容性和与天然组织细胞外基质的结构相似性,选择藻酸盐 (ALG) 作为墨水来生产可定制的 3D 牺牲性微结构。ALG 结构进一步通过生物指令性壳聚糖和精氨酸-甘氨酸-天冬氨酸偶联的 ALG 多层进行 LbL 涂层,嵌入剪切稀化光交联黄原胶水凝胶中,并暴露于钙螯合溶液中以形成可灌注的多层微通道,模拟了生物屏障,如基底膜,内皮细胞在其中播种,表明增强了细胞黏附性。这些 3D 构建体为工程模块化 TERM 策略的各种大型 3D 血管化组织构建体提供了巨大的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/2d140e014382/biomolecules-11-00863-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/3a4e3cea21d8/biomolecules-11-00863-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/14fd2569cefa/biomolecules-11-00863-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/e7dcb3c62892/biomolecules-11-00863-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/eb73633172b9/biomolecules-11-00863-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/b08c6a3ec61a/biomolecules-11-00863-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/a2469c972ed4/biomolecules-11-00863-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/2d140e014382/biomolecules-11-00863-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/3a4e3cea21d8/biomolecules-11-00863-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/14fd2569cefa/biomolecules-11-00863-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/e7dcb3c62892/biomolecules-11-00863-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/eb73633172b9/biomolecules-11-00863-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/b08c6a3ec61a/biomolecules-11-00863-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/a2469c972ed4/biomolecules-11-00863-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2f/8230362/2d140e014382/biomolecules-11-00863-g007.jpg

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