TY - JOUR
T1 - Biomimetic Scaffolds Modulate the Posttraumatic Inflammatory Response in Articular Cartilage Contributing to Enhanced Neoformation of Cartilaginous Tissue In Vivo
AU - Bauza-Mayol, Guillermo
AU - Quintela, Marcos
AU - Brozovich, Ava
AU - Hopson, Michael
AU - Shaikh, Shazad
AU - Cabrera, Fernando
AU - Shi, Aaron
AU - Niclot, Federica Banche
AU - Paradiso, Francesca
AU - Combellack, Emman
AU - Jovic, Tom
AU - Rees, Paul
AU - Tasciotti, Ennio
AU - Francis, Lewis W.
AU - Mcculloch, Patrick
AU - Taraballi, Francesca
N1 - Funding Information:
The authors acknowledge the HMRI MRI core and Dr. Christof Karmonik for his help in the protocol setting. The authors also acknowledge the Center for Immunotherapy Research and the Director Prof. Shu-Hsia Chen for helping with CyTOF analysis and Dr. David James for the statistical analysis. This study was supported by the Cullen Trust for Health Care Foundation, Project ID: 18130014 (E.T.), a pilot project grant by the Department of Orthopedics of the Houston Methodist Hospital (F.T., P.M.). The authors thank Dr Aijun Zhang, Dr. Richard Cole and Dr. Douglas Sieglaff from the bioinformatics department at Houston Methodist Research Institute for their advice in the RNA sequencing process.
Funding Information:
The authors acknowledge the HMRI MRI core and Dr. Christof Karmonik for his help in the protocol setting. The authors also acknowledge the Center for Immunotherapy Research and the Director Prof. Shu‐Hsia Chen for helping with CyTOF analysis and Dr. David James for the statistical analysis. This study was supported by the Cullen Trust for Health Care Foundation, Project ID: 18130014 (E.T.), a pilot project grant by the Department of Orthopedics of the Houston Methodist Hospital (F.T., P.M.). The authors thank Dr Aijun Zhang, Dr. Richard Cole and Dr. Douglas Sieglaff from the bioinformatics department at Houston Methodist Research Institute for their advice in the RNA sequencing process.
Publisher Copyright:
© 2021 The Authors. Advanced Healthcare Materials published by Wiley-VCH GmbH
Copyright:
Copyright 2022 Elsevier B.V., All rights reserved.
PY - 2022/1/5
Y1 - 2022/1/5
N2 - Focal chondral lesions of the knee are the most frequent type of trauma in younger patients and are associated with a high risk of developing early posttraumatic osteoarthritis. The only current clinical solutions include microfracture, osteochondral grafting, and autologous chondrocyte implantation. Cartilage tissue engineering based on biomimetic scaffolds has become an appealing strategy to repair cartilage defects. Here, a chondrogenic collagen-chondroitin sulfate scaffold is tested in an orthotopic Lapine in vivo model to understand the beneficial effects of the immunomodulatory biomaterial on the full chondral defect. Using a combination of noninvasive imaging techniques, histological and whole transcriptome analysis, the scaffolds are shown to enhance the formation of cartilaginous tissue and suppression of host cartilage degeneration, while also supporting tissue integration and increased tissue regeneration over a 12 weeks recovery period. The results presented suggest that biomimetic materials could be a clinical solution for cartilage tissue repair, due to their ability to modulate the immune environment in favor of regenerative processes and suppression of cartilage degeneration.
AB - Focal chondral lesions of the knee are the most frequent type of trauma in younger patients and are associated with a high risk of developing early posttraumatic osteoarthritis. The only current clinical solutions include microfracture, osteochondral grafting, and autologous chondrocyte implantation. Cartilage tissue engineering based on biomimetic scaffolds has become an appealing strategy to repair cartilage defects. Here, a chondrogenic collagen-chondroitin sulfate scaffold is tested in an orthotopic Lapine in vivo model to understand the beneficial effects of the immunomodulatory biomaterial on the full chondral defect. Using a combination of noninvasive imaging techniques, histological and whole transcriptome analysis, the scaffolds are shown to enhance the formation of cartilaginous tissue and suppression of host cartilage degeneration, while also supporting tissue integration and increased tissue regeneration over a 12 weeks recovery period. The results presented suggest that biomimetic materials could be a clinical solution for cartilage tissue repair, due to their ability to modulate the immune environment in favor of regenerative processes and suppression of cartilage degeneration.
KW - Biomimetics
KW - Cartilage, Articular
KW - Chondrocytes
KW - Chondrogenesis
KW - Humans
KW - Tissue Engineering
KW - Tissue Scaffolds
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U2 - 10.1002/adhm.202101127
DO - 10.1002/adhm.202101127
M3 - Article
C2 - 34662505
AN - SCOPUS:85117885944
SN - 2192-2640
VL - 11
SP - e2101127
JO - Advanced Healthcare Materials
JF - Advanced Healthcare Materials
IS - 1
M1 - 2101127
ER -