TY - JOUR
T1 - Serum-free manufacturing of mesenchymal stem cell tissue rings using human-induced pluripotent stem cells
AU - Winston, Tackla S.
AU - Suddhapas, Kantaphon
AU - Wang, Chenyan
AU - Ramos, Rafael
AU - Soman, Pranav
AU - Ma, Zhen
N1 - Funding Information:
This work was supported by the National Science Foundation (NSF EBMS-1804875), the Nappi Family Foundation Research Scholar Project, and SU Collaboration for Unprecedented Success and Excellence (CUSE) Grant. Z. M. acknowledges the support from Lush Prize Young Researchers at Americas. T. W. acknowledges the support from Syracuse University STEM fellowship. We acknowledge the hiPSC line provided by Prof. Conklin from Gladstone Institute. We acknowledge the help from Jessica McDonald’s Lab in the Department of Biology for tissue histology. We acknowledge the help from Zhaowei Jiang at Syracuse Flow Core for flow cytometry analysis.
Publisher Copyright:
Copyright © 2019 Tackla S. Winston et al.
PY - 2019
Y1 - 2019
N2 - Combination of stem cell technology and 3D biofabrication approaches provides physiological similarity to in vivo tissues and the capability of repairing and regenerating damaged human tissues. Mesenchymal stem cells (MSCs) have been widely used for regenerative medicine applications because of their immunosuppressive properties and multipotent potentials. To obtain large amount of high-quality MSCs without patient donation and invasive procedures, we differentiated MSCs from human-induced pluripotent stem cells (hiPSC-MSCs) using serum-free E6 media supplemented with only one growth factor (bFGF) and two small molecules (SB431542 and CHIR99021). The differentiated cells showed a high expression of common MSC-specific surface markers (CD90, CD73, CD105, CD106, CD146, and CD166) and a high potency for osteogenic and chondrogenic differentiation. With these cells, we have been able to manufacture MSC tissue rings with high consistency and robustness in pluronic-coated reusable PDMS devices. The MSC tissue rings were characterized based on inner diameter and outer ring diameter and observed cell-type-dependent tissue contraction induced by cell-matrix interaction. Our approach of simplified hiPSC-MSC differentiation, modular fabrication procedure, and serum-free culture conditions has a great potential for scalable manufacturing of MSC tissue rings for different regenerative medicine applications.
AB - Combination of stem cell technology and 3D biofabrication approaches provides physiological similarity to in vivo tissues and the capability of repairing and regenerating damaged human tissues. Mesenchymal stem cells (MSCs) have been widely used for regenerative medicine applications because of their immunosuppressive properties and multipotent potentials. To obtain large amount of high-quality MSCs without patient donation and invasive procedures, we differentiated MSCs from human-induced pluripotent stem cells (hiPSC-MSCs) using serum-free E6 media supplemented with only one growth factor (bFGF) and two small molecules (SB431542 and CHIR99021). The differentiated cells showed a high expression of common MSC-specific surface markers (CD90, CD73, CD105, CD106, CD146, and CD166) and a high potency for osteogenic and chondrogenic differentiation. With these cells, we have been able to manufacture MSC tissue rings with high consistency and robustness in pluronic-coated reusable PDMS devices. The MSC tissue rings were characterized based on inner diameter and outer ring diameter and observed cell-type-dependent tissue contraction induced by cell-matrix interaction. Our approach of simplified hiPSC-MSC differentiation, modular fabrication procedure, and serum-free culture conditions has a great potential for scalable manufacturing of MSC tissue rings for different regenerative medicine applications.
UR - http://www.scopus.com/inward/record.url?scp=85065814869&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85065814869&partnerID=8YFLogxK
U2 - 10.1155/2019/5654324
DO - 10.1155/2019/5654324
M3 - Article
AN - SCOPUS:85065814869
SN - 1687-966X
VL - 2019
JO - Stem Cells International
JF - Stem Cells International
M1 - 5654324
ER -