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3D bioprinting strategy for engineering vascularized tissue models

Leveraging three-dimensional (3D) bioprinting in the fields of tissue engineering and regenerative medicine has rapidly accelerated progress toward the development of living tissue constructs and biomedical devices. Ongoing vigorous research has pursued the development of 3D in vitro tissue models t...

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Autores principales: Chae, Suhun, Ha, Dong-Heon, Lee, Hyungseok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Whioce Publishing Pte. Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370342/
https://www.ncbi.nlm.nih.gov/pubmed/37502273
http://dx.doi.org/10.18063/ijb.748
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author Chae, Suhun
Ha, Dong-Heon
Lee, Hyungseok
author_facet Chae, Suhun
Ha, Dong-Heon
Lee, Hyungseok
author_sort Chae, Suhun
collection PubMed
description Leveraging three-dimensional (3D) bioprinting in the fields of tissue engineering and regenerative medicine has rapidly accelerated progress toward the development of living tissue constructs and biomedical devices. Ongoing vigorous research has pursued the development of 3D in vitro tissue models to replicate the key aspects of human physiology by incorporating relevant cell populations and adequate environmental cues. Given their advantages of being able to intimately mimic the heterogeneity and complexity of their native counterparts, 3D in vitro models hold promise as alternatives to conventional cell cultures or animal models for translational application to model human physiology/pathology and drug screening. Research has highlighted the importance of in vitro models, and a sophisticated biomanufacturing strategy is vitally required. In particular, vascularization is critical for the prolonged survival and functional maturation of the engineered tissues, which has remained one of the major challenges in the establishment of physiologically relevant 3D in vitro models. To this end, 3D bioprinting can efficiently generate solid and reproducible vascularized tissue models with high architectural and compositional similarity to the native tissues, leading to improve the structural maturation and tissue-specific functionality. Multiple bioprinting strategies have been developed to vascularize in vitro tissues by spatially controlled patterning of vascular precursors or generating readily perfusable vascular structures. This review presents an overview of the advanced 3D bioprinting strategies for vascularized tissue model development. We present the key elements for rebuilding functional vasculature in 3D-bioprinted tissue models and discuss the recent achievements in the engineering of 3D vascularized in vitro models using 3D bioprinting. Finally, we delineate the current challenges and future outlooks of 3D bioprinting-based vascularized tissue models.
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spelling pubmed-103703422023-07-27 3D bioprinting strategy for engineering vascularized tissue models Chae, Suhun Ha, Dong-Heon Lee, Hyungseok Int J Bioprint Review Article Leveraging three-dimensional (3D) bioprinting in the fields of tissue engineering and regenerative medicine has rapidly accelerated progress toward the development of living tissue constructs and biomedical devices. Ongoing vigorous research has pursued the development of 3D in vitro tissue models to replicate the key aspects of human physiology by incorporating relevant cell populations and adequate environmental cues. Given their advantages of being able to intimately mimic the heterogeneity and complexity of their native counterparts, 3D in vitro models hold promise as alternatives to conventional cell cultures or animal models for translational application to model human physiology/pathology and drug screening. Research has highlighted the importance of in vitro models, and a sophisticated biomanufacturing strategy is vitally required. In particular, vascularization is critical for the prolonged survival and functional maturation of the engineered tissues, which has remained one of the major challenges in the establishment of physiologically relevant 3D in vitro models. To this end, 3D bioprinting can efficiently generate solid and reproducible vascularized tissue models with high architectural and compositional similarity to the native tissues, leading to improve the structural maturation and tissue-specific functionality. Multiple bioprinting strategies have been developed to vascularize in vitro tissues by spatially controlled patterning of vascular precursors or generating readily perfusable vascular structures. This review presents an overview of the advanced 3D bioprinting strategies for vascularized tissue model development. We present the key elements for rebuilding functional vasculature in 3D-bioprinted tissue models and discuss the recent achievements in the engineering of 3D vascularized in vitro models using 3D bioprinting. Finally, we delineate the current challenges and future outlooks of 3D bioprinting-based vascularized tissue models. Whioce Publishing Pte. Ltd. 2023-03-09 /pmc/articles/PMC10370342/ /pubmed/37502273 http://dx.doi.org/10.18063/ijb.748 Text en Copyright:© 2023, Chae S, Ha D-H, Lee H https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, permitting distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Chae, Suhun
Ha, Dong-Heon
Lee, Hyungseok
3D bioprinting strategy for engineering vascularized tissue models
title 3D bioprinting strategy for engineering vascularized tissue models
title_full 3D bioprinting strategy for engineering vascularized tissue models
title_fullStr 3D bioprinting strategy for engineering vascularized tissue models
title_full_unstemmed 3D bioprinting strategy for engineering vascularized tissue models
title_short 3D bioprinting strategy for engineering vascularized tissue models
title_sort 3d bioprinting strategy for engineering vascularized tissue models
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370342/
https://www.ncbi.nlm.nih.gov/pubmed/37502273
http://dx.doi.org/10.18063/ijb.748
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