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脱细胞基质定向冰模板支架中的图案化血管生成。

Patterned vascularization in a directional ice-templated scaffold of decellularized matrix.

作者信息

Shen Li, Song Xiuyue, Xu Yalan, Tian Runhua, Wang Yin, Li Peifeng, Li Jing, Bai Hao, Zhu Hai, Wang Dong

机构信息

Institute for Translational Medicine The Affiliated Hospital of Qingdao University Medical College Qingdao University Qingdao P. R. China.

School of Basic Medicine Qingdao University Qingdao P. R. China.

出版信息

Eng Life Sci. 2021 Jul 1;21(10):683-692. doi: 10.1002/elsc.202100034. eCollection 2021 Oct.

DOI:10.1002/elsc.202100034
PMID:34690638
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8518570/
Abstract

Vascularization is fundamental for large-scale tissue engineering. Most of the current vascularization strategies including microfluidics and three-dimensional (3D) printing aim to precisely fabricate microchannels for individual microvessels. However, few studies have examined the remodeling capacity of the microvessels in the engineered constructs, which is important for transplantation in vivo. Here we present a method for patterning microvessels in a directional ice-templated scaffold of decellularized porcine kidney extracellular matrix. The aligned microchannels made by directional ice templating allowed for fast and efficient cell seeding. The pure decellularized matrix without any fixatives or cross-linkers maximized the potential of tissue remodeling. Dramatical microvascular remodeling happened in the scaffold in 2 weeks, from small primary microvessel segments to long patterned microvessels. The majority of the microvessels were aligned in parallel and interconnected with each other to form a network. This method is compatible with other engineering techniques, such as microfluidics and 3D printing, and multiple cell types can be co-cultured to make complex vascularized tissue and organ models.

摘要

血管化对于大规模组织工程至关重要。当前大多数血管化策略,包括微流控技术和三维(3D)打印,旨在精确制造单个微血管的微通道。然而,很少有研究考察工程构建体中微血管的重塑能力,而这对于体内移植很重要。在此,我们展示了一种在脱细胞猪肾细胞外基质的定向冰模板支架中对微血管进行图案化的方法。通过定向冰模板制作的排列微通道允许快速高效地接种细胞。不含任何固定剂或交联剂的纯脱细胞基质使组织重塑的潜力最大化。在两周内支架中发生了显著的微血管重塑,从小的初级微血管段变成了长的图案化微血管。大多数微血管相互平行排列并相互连接形成网络。这种方法与其他工程技术兼容,如微流控技术和3D打印,并且可以共培养多种细胞类型以制作复杂的血管化组织和器官模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/20c75f8798d8/ELSC-21-683-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/823f5bdd0332/ELSC-21-683-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/cc6b601e68fe/ELSC-21-683-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/c21d006aca15/ELSC-21-683-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/dec0ae8001a8/ELSC-21-683-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/5bca290a6267/ELSC-21-683-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/20c75f8798d8/ELSC-21-683-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/823f5bdd0332/ELSC-21-683-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/cc6b601e68fe/ELSC-21-683-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/c21d006aca15/ELSC-21-683-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/dec0ae8001a8/ELSC-21-683-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/5bca290a6267/ELSC-21-683-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3d1/8518570/20c75f8798d8/ELSC-21-683-g006.jpg

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Defining Endothelial Cell-Derived Factors That Promote Pericyte Recruitment and Capillary Network Assembly.
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