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Microcomputed Tomography-Based Analysis of Neovascularization within Bioengineered Vascularized Tissues.

Authors :
Redenski I
Guo S
Machour M
Szklanny A
Landau S
Egozi D
Gabet Y
Levenberg S
Source :
ACS biomaterials science & engineering [ACS Biomater Sci Eng] 2022 Jan 10; Vol. 8 (1), pp. 232-241. Date of Electronic Publication: 2021 Dec 14.
Publication Year :
2022

Abstract

In the field of tissue engineering, evaluating newly formed vascular networks is considered a fundamental step in deciphering the processes underlying tissue development. Several common modalities exist to study vessel network formation and function. However, a proper methodology that allows through three-dimensional visualization of neovessels in a reproducible manner is required. Here, we describe in-depth exploration, visualization, and analysis of vessels within newly formed tissues by utilizing a contrast agent perfusion protocol and high-resolution microcomputed tomography. Bioengineered constructs consisting of porous, biocompatible, and biodegradable scaffolds are loaded with cocultures of adipose-derived microvascular endothelial cells (HAMECs) and dental pulp stem cells (DPSCs) and implanted in a rat femoral bundle model. After 14 days of in vivo maturation, we performed the optimized perfusion protocol to allow host penetrating vascular visualization and assessment within neotissues. Following high-resolution microCT scanning of DPSC:HAMEC explants, we performed the volumetric and spatial analysis of neovasculature. Eventually, the process was repeated with a previously published coculture system for prevascularization based on adipose-derived mesenchymal stromal cells (MSCs) and HAMECs. Overall, our approach allows a comprehensive understanding of vessel organization during engraftment and development of neotissues.

Details

Language :
English
ISSN :
2373-9878
Volume :
8
Issue :
1
Database :
MEDLINE
Journal :
ACS biomaterials science & engineering
Publication Type :
Academic Journal
Accession number :
34905338
Full Text :
https://doi.org/10.1021/acsbiomaterials.1c01401