3D bioprinting of collagen-based high-resolution internally perfusable scaffolds for engineering fully biologic tissue systems

Organ-on-a-chip and microfluidic systems have improved the translational relevance of in vitro systems; however, current manufacturing approaches impart limitations on materials selection, non-native mechanical properties, geometric complexity, and cell-driven remodeling into functional tissues. Here, we three-dimensionally (3D) bioprint extracellular matrix (ECM) and cells into collagen-based high-resolution internally perfusable scaffolds (CHIPS) that integrate with a vascular and perfusion organ-on-a-chip reactor (VAPOR) to form a complete tissue engineering platform. We improve the fidelity of freeform reversible embedding of suspended hydrogels (FRESH) bioprinting to produce a range of CHIPS designs fabricated in a one-step process. CHIPS exhibit size-dependent permeability of perfused molecules into the surrounding scaffold to support cell viability and migration. Lastly, we implemented multi-material bioprinting to control 3D spatial patterning, ECM composition, cellularization, and material properties to create a glucose-responsive, insulin-secreting pancreatic-like CHIPS with vascular endothelial cadherin<sup>+</sup> vascular-like networks. Together, CHIPS and VAPOR form a platform technology toward engineering full organ-scale function for disease modeling and cell replacement therapy.

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Publication Details

Journal
Science Advances
Published
2025-04-23
DOI
https://doi.org/10.1126/sciadv.adu5905
Citations
55
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
37.08
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article

3D bioprinting of collagen-based high-resolution internally perfusable scaffolds for engineering fully biologic tissue systems

Daniel J. Shiwarski, Andrew R. Hudson, Joshua W. Tashman, Ezgi Bakırcı et al.
55 citations
Science Advances
3D Printing in Biomedical Research
37.08
article

3D bioprinting of collagen-based high-resolution internally perfusable scaffolds for engineering fully biologic tissue systems

Daniel J. Shiwarski, Andrew R. Hudson, Joshua W. Tashman, Ezgi Bakırcı, Brian Coffin, Adam W. Feinberg, Samuel Moss
article en
55 citations

Abstract

Organ-on-a-chip and microfluidic systems have improved the translational relevance of in vitro systems; however, current manufacturing approaches impart limitations on materials selection, non-native mechanical properties, geometric complexity, and cell-driven remodeling into functional tissues. Here, we three-dimensionally (3D) bioprint extracellular matrix (ECM) and cells into collagen-based high-resolution internally perfusable scaffolds (CHIPS) that integrate with a vascular and perfusion organ-on-a-chip reactor (VAPOR) to form a complete tissue engineering platform. We improve the fidelity of freeform reversible embedding of suspended hydrogels (FRESH) bioprinting to produce a range of CHIPS designs fabricated in a one-step process. CHIPS exhibit size-dependent permeability of perfused molecules into the surrounding scaffold to support cell viability and migration. Lastly, we implemented multi-material bioprinting to control 3D spatial patterning, ECM composition, cellularization, and material properties to create a glucose-responsive, insulin-secreting pancreatic-like CHIPS with vascular endothelial cadherin<sup>+</sup> vascular-like networks. Together, CHIPS and VAPOR form a platform technology toward engineering full organ-scale function for disease modeling and cell replacement therapy.

Science AdvancesVol. 11(17)
University of Pittsburgh (US), Carnegie Mellon University (US)
Openalex Percentile: Top 0%
3D Printing in Biomedical Research
37.08
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