TY - JOUR
T1 - Decellularized Porcine Cartilage Scaffold
T2 - Validation of Decellularization and Evaluation of Biomarkers of Chondrogenesis
AU - Stone, Roxanne N.
AU - Frahs, Stephanie M.
AU - Hardy, Makenna J.
AU - Fujimoto, Akina
AU - Pu, Xinzhu
AU - Keller‐peck, Cynthia
AU - Oxford, Julia Thom
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/6
Y1 - 2021/6
N2 - Osteoarthritis is a major concern in the United States and worldwide. Current non‐surgical and surgical approaches alleviate pain but show little evidence of cartilage restoration. Cell‐based treatments may hold promise for the regeneration of hyaline cartilage‐like tissue at the site of injury or wear. Cell–cell and cell–matrix interactions have been shown to drive cell differentiation path-ways. Biomaterials for clinically relevant applications can be generated from decellularized porcine auricular cartilage. This material may represent a suitable scaffold on which to seed and grow chon-drocytes to create new cartilage. In this study, we used decellularization techniques to create an extracellular matrix scaffold that supports chondrocyte cell attachment and growth in tissue culture conditions. Results presented here evaluate the decellularization process histologically and molec-ularly. We identified new and novel biomarker profiles that may aid future cartilage decellulariza-tion efforts. Additionally, the resulting scaffold was characterized using scanning electron micros-copy, fluorescence microscopy, and proteomics. Cellular response to the decellularized scaffold was evaluated by quantitative real‐time PCR for gene expression analysis.
AB - Osteoarthritis is a major concern in the United States and worldwide. Current non‐surgical and surgical approaches alleviate pain but show little evidence of cartilage restoration. Cell‐based treatments may hold promise for the regeneration of hyaline cartilage‐like tissue at the site of injury or wear. Cell–cell and cell–matrix interactions have been shown to drive cell differentiation path-ways. Biomaterials for clinically relevant applications can be generated from decellularized porcine auricular cartilage. This material may represent a suitable scaffold on which to seed and grow chon-drocytes to create new cartilage. In this study, we used decellularization techniques to create an extracellular matrix scaffold that supports chondrocyte cell attachment and growth in tissue culture conditions. Results presented here evaluate the decellularization process histologically and molec-ularly. We identified new and novel biomarker profiles that may aid future cartilage decellulariza-tion efforts. Additionally, the resulting scaffold was characterized using scanning electron micros-copy, fluorescence microscopy, and proteomics. Cellular response to the decellularized scaffold was evaluated by quantitative real‐time PCR for gene expression analysis.
KW - C28/I2 cells
KW - Cartilage
KW - Chondrocytes
KW - Decellularized
KW - Histology
KW - Porcine auricular cartilage
KW - Proteomics
KW - Real time quantitative PCR
KW - Scaffold
KW - Scanning electron microscopy
UR - http://www.scopus.com/inward/record.url?scp=85107405103&partnerID=8YFLogxK
UR - https://scholarworks.boisestate.edu/bio_facpubs/687/
U2 - 10.3390/ijms22126241
DO - 10.3390/ijms22126241
M3 - Article
C2 - 34207917
SN - 1661-6596
VL - 22
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 12
M1 - 6241
ER -