TY - JOUR
T1 - 3D Bioprinting of human Mesenchymal Stem Cells in a novel tunic decellularized ECM bioink for Cartilage Tissue Engineering
AU - Govindharaj, Mano
AU - Hashimi, Noura Al
AU - Soman, Soja Saghar
AU - Kanwar, Susheem
AU - Vijayavenkataraman, Sanjairaj
N1 - Funding Information:
The research was funded by the NYUAD start up grant for Sanjairaj Vijayavenkataraman.
Funding Information:
The raw/processed data required to reproduce these findings cannot be shared at this time as the data also forms part of an ongoing study. The research was funded by the NYUAD start up grant for Sanjairaj Vijayavenkataraman. This research was partially carried out using the Core Technology Platforms resources at New York University Abu Dhabi.
Publisher Copyright:
© 2022
PY - 2022/6
Y1 - 2022/6
N2 - Tunicates are marine organisms renowned for their thick, leathery exoskeleton called tunic. This tunic is composed of an extracellular matrix packed with protein-cellulose complexes and sulfated polysaccharides, making it a charming biomaterial choice for cartilage tissue engineering. In this study, P.nigra tunicate was collected and processed to obtain its rich decellularized extracellular matrix (dECM). The dECM was either seeded with human mesenchymal stem cells (hMSCs) as is or underwent further processing to form a hydrogel for 3D bioprinting. The characterization of tunic dECM was achieved by FTIR, XRD, TGA, Raman spectroscopy, SEM and tensile mechanical analysis. Biological compatibility and staining were done by live/dead, alamar blue, alcian blue, safranin O and PCR gene expression. After decellularization, the tunic dECM scaffold preserved the natural honeycomb-shaped microstructure, as well as its functional cellulose and protein groups. Both the tunic dECM scaffolds and bioprinted scaffolds showed enhanced metabolic activity, cell proliferation and chondrogenic differentiation. Combining both the mechanical robustness and biocompatibility, the bioink is able to fill the elusive gap in cartilage regeneration. This study offers a new potential source of dECM scaffolds and bioinks which are both biologically compatible and mechanically stable, making it a one stop shop for cartilage tissue engineering.
AB - Tunicates are marine organisms renowned for their thick, leathery exoskeleton called tunic. This tunic is composed of an extracellular matrix packed with protein-cellulose complexes and sulfated polysaccharides, making it a charming biomaterial choice for cartilage tissue engineering. In this study, P.nigra tunicate was collected and processed to obtain its rich decellularized extracellular matrix (dECM). The dECM was either seeded with human mesenchymal stem cells (hMSCs) as is or underwent further processing to form a hydrogel for 3D bioprinting. The characterization of tunic dECM was achieved by FTIR, XRD, TGA, Raman spectroscopy, SEM and tensile mechanical analysis. Biological compatibility and staining were done by live/dead, alamar blue, alcian blue, safranin O and PCR gene expression. After decellularization, the tunic dECM scaffold preserved the natural honeycomb-shaped microstructure, as well as its functional cellulose and protein groups. Both the tunic dECM scaffolds and bioprinted scaffolds showed enhanced metabolic activity, cell proliferation and chondrogenic differentiation. Combining both the mechanical robustness and biocompatibility, the bioink is able to fill the elusive gap in cartilage regeneration. This study offers a new potential source of dECM scaffolds and bioinks which are both biologically compatible and mechanically stable, making it a one stop shop for cartilage tissue engineering.
KW - Bioprinting
KW - Marine biomaterials
KW - bioink
KW - cartilage tissue engineering
KW - extracellular matrix
KW - hydrogel
KW - tunicates
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U2 - 10.1016/j.mtla.2022.101457
DO - 10.1016/j.mtla.2022.101457
M3 - Article
AN - SCOPUS:85134036114
SN - 2589-1529
VL - 23
JO - Materialia
JF - Materialia
M1 - 101457
ER -