Rapid Volumetric Bioprinting of Decellularized Extracellular Matrix Bioinks

Author:

Lian Liming1,Xie Maobin1,Luo Zeyu1,Zhang Zhenrui12,Maharjan Sushila1,Mu Xuan1,Garciamendez‐Mijares Carlos Ezio1,Kuang Xiao1,Sahoo Jugal Kishore3,Tang Guosheng1,Li Gang3,Wang Di1,Guo Jie1,González Federico Zertuche1,Abril Manjarrez Rivera Victoria1,Cai Ling1,Mei Xuan1,Kaplan David L.3,Zhang Yu Shrike1ORCID

Affiliation:

1. Division of Engineering in Medicine Department of Medicine Brigham and Women's Hospital Harvard Medical School Cambridge MA 02139 USA

2. Ragon Institute of Mass General, MIT, and Harvard Cambridge MA 02139 USA

3. Department of Biomedical Engineering Tufts University Medford MA 02155 USA

Abstract

AbstractDecellularized extracellular matrix (dECM)‐based hydrogels are widely applied to additive biomanufacturing strategies for relevant applications. The extracellular matrix components and growth factors of dECM play crucial roles in cell adhesion, growth, and differentiation. However, the generally poor mechanical properties and printability have remained as major limitations for dECM‐based materials. In this study, heart‐derived dECM (h‐dECM) and meniscus‐derived dECM (Ms‐dECM) bioinks in their pristine, unmodified state supplemented with the photoinitiator system of tris(2,2‐bipyridyl) dichlororuthenium(II) hexahydrate and sodium persulfate, demonstrate cytocompatibility with volumetric bioprinting processes. This recently developed bioprinting modality illuminates a dynamically evolving light pattern into a rotating volume of the bioink, and thus decouples the requirement of mechanical strengths of bioprinted hydrogel constructs with printability, allowing for the fabrication of sophisticated shapes and architectures with low‐concentration dECM materials that set within tens of seconds. As exemplary applications, cardiac tissues are volumetrically bioprinted using the cardiomyocyte‐laden h‐dECM bioink showing favorable cell proliferation, expansion, spreading, biomarker expressions, and synchronized contractions; whereas the volumetrically bioprinted Ms‐dECM meniscus structures embedded with human mesenchymal stem cells present appropriate chondrogenic differentiation outcomes. This study supplies expanded bioink libraries for volumetric bioprinting and broadens utilities of dECM toward tissue engineering and regenerative medicine.

Funder

National Institutes of Health

National Science Foundation

Army Research Office

Air Force Office of Scientific Research

Chan Zuckerberg Initiative

Brigham Research Institute

Foundation for the National Institutes of Health

Publisher

Wiley

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