TY - JOUR
T1 - Preparation and Endothelialization of Multi-level Vessel-like Network in Enzymated Gelatin Scaffolds
AU - Dong, Guirong
AU - Lian, Qin
AU - Yang, Laixia
AU - Mao, Wei
AU - Liu, Shiyang
AU - Xu, Chao
N1 - Publisher Copyright:
© 2018, Jilin University.
PY - 2018/7/1
Y1 - 2018/7/1
N2 - Loss of function of large tissues is an urgent clinical problem. Although the artificial microfluidic network fabricated in large tissue- engineered constructs has great promise, it is still difficult to develop an efficient vessel-like design to meet the requirements of the biomimetic vascular network for tissue engineering applications. In this study, we used a facile approach to fabricate a branched and multi-level vessel-like network in a large muscle scaffolds by combining stereolithography (SL) technology and enzymatic crosslinking mechanism. The morphology of microchannel cross-sections was characterized using micro-computed tomography. The square cross-sections were gradually changed to a seamless circular microfluidic network, which is similar to the natural blood vessel. In the different micro-channels, the velocity greatly affected the attachment and spread of Human Umbilical Vein Endothelial Cell (HUVEC)-Green Fluorescent Protein (GFP). Our study demonstrated that the branched and multi-level microchannel network simulates biomimetic microenvironments to promote endothelialization. The gelatin scaffolds in the circular vessel-like networks will likely support myoblast and surrounding tissue for clinical use.
AB - Loss of function of large tissues is an urgent clinical problem. Although the artificial microfluidic network fabricated in large tissue- engineered constructs has great promise, it is still difficult to develop an efficient vessel-like design to meet the requirements of the biomimetic vascular network for tissue engineering applications. In this study, we used a facile approach to fabricate a branched and multi-level vessel-like network in a large muscle scaffolds by combining stereolithography (SL) technology and enzymatic crosslinking mechanism. The morphology of microchannel cross-sections was characterized using micro-computed tomography. The square cross-sections were gradually changed to a seamless circular microfluidic network, which is similar to the natural blood vessel. In the different micro-channels, the velocity greatly affected the attachment and spread of Human Umbilical Vein Endothelial Cell (HUVEC)-Green Fluorescent Protein (GFP). Our study demonstrated that the branched and multi-level microchannel network simulates biomimetic microenvironments to promote endothelialization. The gelatin scaffolds in the circular vessel-like networks will likely support myoblast and surrounding tissue for clinical use.
KW - endothelialization
KW - enzymatically gelatin hydrogel
KW - large-size scaffolds
KW - muscle tissue engineering
KW - vascular network
UR - https://www.scopus.com/pages/publications/85049569194
U2 - 10.1007/s42235-018-0055-3
DO - 10.1007/s42235-018-0055-3
M3 - 文章
AN - SCOPUS:85049569194
SN - 1672-6529
VL - 15
SP - 673
EP - 681
JO - Journal of Bionic Engineering
JF - Journal of Bionic Engineering
IS - 4
ER -