Extracellular-Matrix-Reinforced Bioinks for 3D Bioprinting Human Tissue
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Extracellular-Matrix-Reinforced Bioinks for 3D Bioprinting Human Tissue. / De Santis, Martina M; Alsafadi, Hani N; Tas, Sinem; Bölükbas, Deniz A; Prithiviraj, Sujeethkumar; Da Silva, Iran A; Mittendorfer, Margareta; Ota, Chiharu; Stegmayr, John; Daoud, Fatima; Königshoff, Melanie; Swärd, Karl; Wood, Jeffery A; Tassieri, Manlio; Bourgine, Paul E; Lindstedt, Sandra; Mohlin, Sofie; Wagner, Darcy E.
In: Advanced Materials, 09.12.2020.Research output: Contribution to journal › Article
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T1 - Extracellular-Matrix-Reinforced Bioinks for 3D Bioprinting Human Tissue
AU - De Santis, Martina M
AU - Alsafadi, Hani N
AU - Tas, Sinem
AU - Bölükbas, Deniz A
AU - Prithiviraj, Sujeethkumar
AU - Da Silva, Iran A
AU - Mittendorfer, Margareta
AU - Ota, Chiharu
AU - Stegmayr, John
AU - Daoud, Fatima
AU - Königshoff, Melanie
AU - Swärd, Karl
AU - Wood, Jeffery A
AU - Tassieri, Manlio
AU - Bourgine, Paul E
AU - Lindstedt, Sandra
AU - Mohlin, Sofie
AU - Wagner, Darcy E
N1 - © 2020 The Authors. Advanced Materials published by Wiley-VCH GmbH.
PY - 2020/12/9
Y1 - 2020/12/9
N2 - Recent advances in 3D bioprinting allow for generating intricate structures with dimensions relevant for human tissue, but suitable bioinks for producing translationally relevant tissue with complex geometries remain unidentified. Here, a tissue-specific hybrid bioink is described, composed of a natural polymer, alginate, reinforced with extracellular matrix derived from decellularized tissue (rECM). rECM has rheological and gelation properties beneficial for 3D bioprinting while retaining biologically inductive properties supporting tissue maturation ex vivo and in vivo. These bioinks are shear thinning, resist cell sedimentation, improve viability of multiple cell types, and enhance mechanical stability in hydrogels derived from them. 3D printed constructs generated from rECM bioinks suppress the foreign body response, are pro-angiogenic and support recipient-derived de novo blood vessel formation across the entire graft thickness in a murine model of transplant immunosuppression. Their proof-of-principle for generating human tissue is demonstrated by 3D bioprinting human airways composed of regionally specified primary human airway epithelial progenitor and smooth muscle cells. Airway lumens remained patent with viable cells for one month in vitro with evidence of differentiation into mature epithelial cell types found in native human airways. rECM bioinks are a promising new approach for generating functional human tissue using 3D bioprinting.
AB - Recent advances in 3D bioprinting allow for generating intricate structures with dimensions relevant for human tissue, but suitable bioinks for producing translationally relevant tissue with complex geometries remain unidentified. Here, a tissue-specific hybrid bioink is described, composed of a natural polymer, alginate, reinforced with extracellular matrix derived from decellularized tissue (rECM). rECM has rheological and gelation properties beneficial for 3D bioprinting while retaining biologically inductive properties supporting tissue maturation ex vivo and in vivo. These bioinks are shear thinning, resist cell sedimentation, improve viability of multiple cell types, and enhance mechanical stability in hydrogels derived from them. 3D printed constructs generated from rECM bioinks suppress the foreign body response, are pro-angiogenic and support recipient-derived de novo blood vessel formation across the entire graft thickness in a murine model of transplant immunosuppression. Their proof-of-principle for generating human tissue is demonstrated by 3D bioprinting human airways composed of regionally specified primary human airway epithelial progenitor and smooth muscle cells. Airway lumens remained patent with viable cells for one month in vitro with evidence of differentiation into mature epithelial cell types found in native human airways. rECM bioinks are a promising new approach for generating functional human tissue using 3D bioprinting.
U2 - 10.1002/adma.202005476
DO - 10.1002/adma.202005476
M3 - Article
C2 - 33300242
JO - Advanced Materials
JF - Advanced Materials
SN - 1521-4095
M1 - e2005476
ER -