Document Type
Article
Publication Date
12-2023
Department
Department of Biomedical Engineering
Abstract
Vascularization is a key pre-requisite to engineered anatomical scale three dimensional (3-D) constructs to ensure their nutrient and oxygen supply upon implantation. Presently, engineered pre-vascularized 3-D tissues are limited to only micro-scale hydrogels, which meet neither the anatomical scale needs nor the complexity of natural extracellular matrix (ECM) environments. Anatomical scale perfusable constructs are critically needed for translational applications. To overcome this challenge, we previously developed pre-vascularized ECM sheets with long and oriented dense microvascular networks. The present study further evaluated the patency, perfusability and innate immune response toward these pre-vascularized constructs. Macrophage-co-cultured pre-vascularized constructs were evaluated in vitro to confirm micro-vessel patency and perturbations in macrophage metabolism. Subcutaneously implanted pre-vascularized constructs remained viable and formed a functional anastomosis with host vasculature within 3 days of implantation. This completely biological pre-vascularized construct holds great potential as a building block to engineer perfusable anatomical scale tissues.
Publication Title
Bioactive Materials
Recommended Citation
Sharma, D.,
Sharma, A.,
Hu, L.,
Chen, T.,
Voon, S.,
Bayless, K.,
Goldman, J.,
Walsh, A.,
&
Zhao, F.
(2023).
Perfusability and immunogenicity of implantable pre-vascularized tissues recapitulating features of native capillary network.
Bioactive Materials,
30, 184-199.
http://doi.org/10.1016/j.bioactmat.2023.07.023
Retrieved from: https://digitalcommons.mtu.edu/michigantech-p2/3
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.
Version
Publisher's PDF
Publisher's Statement
© 2023 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. Publisher’s version of record: https://doi.org/10.1016/j.bioactmat.2023.07.023