TY - JOUR
T1 - Decorating 3D Printed Scaffolds with Electrospun Nanofiber Segments for Tissue Engineering
AU - Li, Ruiquan
AU - McCarthy, Alec
AU - Zhang, Yu Shrike
AU - Xie, Jingwei
N1 - Funding Information:
This work was supported by grants from the National Institute of General Medical Science (NIGMS) at the NIH (2P20 GM103480), National Institute of Dental and Craniofacial Research (NIDCR) at the NIH (1R21 DE027516), NE LB606, and regenerative medicine program pilot grants and startup funds from the University of Nebraska Medical Center (UNMC). Y.S.Z. acknowledges support by the NIH (R21EB025270, R21EB026175, R00CA201603, R01EB028143) and the Brigham Research Institute.
Publisher Copyright:
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/12/1
Y1 - 2019/12/1
N2 - Repairing large tissue defects often represents a great challenge in clinics due to issues regarding lack of donors, mismatched sizes, irregular shapes, and immune rejection. 3D printed scaffolds are attractive for growing cells and producing tissue constructs because of the intricate control over pore size, porosity, and geometric shape, but the lack of biomimetic surface nanotopography and limited biomolecule presenting capacity render them less efficacious in regulating cell responses. Herein, a facile method for coating 3D printed scaffolds with electrospun nanofiber segments is reported. The surface morphology of modified 3D scaffolds changes dramatically, displaying a biomimetic nanofibrous structure, while the bulk mechanical property, pore size, and porosity are not significantly compromised. The short nanofibers-decorated 3D printed scaffolds significantly promote adhesion and proliferation of pre-osteoblasts and bone marrow mesenchymal stem cells (BMSCs). Further immobilization of bone morphogenetic protein-2 mimicking peptides to nanofiber segments-decorated 3D printed scaffolds show enhanced mRNA expressions of osteogenic markers Runx2, Alp, OCN, and BSP in BMSCs, indicating the enhancement of BMSCs osteogenic differentiation. Together, the combination of 3D printing and electrospinning is a promising approach to greatly expand the functions of 3D printed scaffolds and enhance the efficacy of 3D printed scaffolds for tissue engineering.
AB - Repairing large tissue defects often represents a great challenge in clinics due to issues regarding lack of donors, mismatched sizes, irregular shapes, and immune rejection. 3D printed scaffolds are attractive for growing cells and producing tissue constructs because of the intricate control over pore size, porosity, and geometric shape, but the lack of biomimetic surface nanotopography and limited biomolecule presenting capacity render them less efficacious in regulating cell responses. Herein, a facile method for coating 3D printed scaffolds with electrospun nanofiber segments is reported. The surface morphology of modified 3D scaffolds changes dramatically, displaying a biomimetic nanofibrous structure, while the bulk mechanical property, pore size, and porosity are not significantly compromised. The short nanofibers-decorated 3D printed scaffolds significantly promote adhesion and proliferation of pre-osteoblasts and bone marrow mesenchymal stem cells (BMSCs). Further immobilization of bone morphogenetic protein-2 mimicking peptides to nanofiber segments-decorated 3D printed scaffolds show enhanced mRNA expressions of osteogenic markers Runx2, Alp, OCN, and BSP in BMSCs, indicating the enhancement of BMSCs osteogenic differentiation. Together, the combination of 3D printing and electrospinning is a promising approach to greatly expand the functions of 3D printed scaffolds and enhance the efficacy of 3D printed scaffolds for tissue engineering.
KW - 3D printed scaffolds
KW - cellular responses
KW - electrospinning
KW - nanofiber segments
KW - surface coating
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U2 - 10.1002/adbi.201900137
DO - 10.1002/adbi.201900137
M3 - Article
C2 - 32648683
AN - SCOPUS:85074757181
SN - 2701-0198
VL - 3
JO - Advanced Biosystems
JF - Advanced Biosystems
IS - 12
M1 - 1900137
ER -