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Osteochondral Injury, Management and Tissue Engineering Approaches.

作者信息

Jacob George, Shimomura Kazunori, Nakamura Norimasa

机构信息

Department of Orthopedic Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.

Department of Orthopedics, Tejasvini Hospital, Mangalore, India.

出版信息

Front Cell Dev Biol. 2020 Nov 4;8:580868. doi: 10.3389/fcell.2020.580868. eCollection 2020.


DOI:10.3389/fcell.2020.580868
PMID:33251212
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7673409/
Abstract

Osteochondral lesions (OL) are a common clinical problem for orthopedic surgeons worldwide and are associated with multiple clinical scenarios ranging from trauma to osteonecrosis. OL vary from chondral lesions in that they involve the subchondral bone and chondral surface, making their management more complex than an isolated chondral injury. Subchondral bone involvement allows for a natural healing response from the body as marrow elements are able to come into contact with the defect site. However, this repair is inadequate resulting in fibrous scar tissue. The second differentiating feature of OL is that damage to the subchondral bone has deleterious effects on the mechanical strength and nutritive capabilities to the chondral joint surface. The clinical solution must, therefore, address both the articular cartilage as well as the subchondral bone beneath it to restore and preserve joint health. Both cartilage and subchondral bone have distinctive functional requirements and therefore their physical and biological characteristics are very much dissimilar, yet they must work together as one unit for ideal joint functioning. In the past, the obvious solution was autologous graft transfer, where an osteochondral bone plug was harvested from a non-weight bearing portion of the joint and implanted into the defect site. Allografts have been utilized similarly to eliminate the donor site morbidity associated with autologous techniques and overall results have been good but both techniques have their drawbacks and limitations. Tissue engineering has thus been an attractive option to create multiphasic scaffolds and implants. Biphasic and triphasic implants have been under explored and have both a chondral and subchondral component with an interface between the two to deliver an implant which is biocompatible and emulates the osteochondral unit as a whole. It has been a challenge to develop such implants and many manufacturing techniques have been utilized to bring together two unalike materials and combine them with cellular therapies. We summarize the functions of the osteochondral unit and describe the currently available management techniques under study.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d45f/7673409/5f10c8edc72f/fcell-08-580868-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d45f/7673409/a31a7cabdb94/fcell-08-580868-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d45f/7673409/f54d84a05f0a/fcell-08-580868-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d45f/7673409/5f10c8edc72f/fcell-08-580868-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d45f/7673409/a31a7cabdb94/fcell-08-580868-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d45f/7673409/f54d84a05f0a/fcell-08-580868-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d45f/7673409/5f10c8edc72f/fcell-08-580868-g003.jpg

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Osteochondral Injury, Management and Tissue Engineering Approaches.

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[2]
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[3]
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[4]
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[5]
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[6]
Application of polydopamine-modified triphasic PLA/PCL-PLGA/Mg(OH)-velvet antler polypeptides scaffold loaded with fibrocartilage stem cells for the repair of osteochondral defects.

Front Bioeng Biotechnol. 2024-9-19

[7]
Drug-Loaded Bioscaffolds for Osteochondral Regeneration.

Pharmaceutics. 2024-8-21

[8]
T1ρ relaxation mapping in osteochondral lesions of the talus: a non-invasive biomarker for altered biomechanical properties of hyaline cartilage?

Eur Radiol Exp. 2024-7-24

[9]
Osteochondral organoids: current advances, applications, and upcoming challenges.

Stem Cell Res Ther. 2024-6-21

[10]
and evaluation of periosteum-derived cells and iPSC-derived chondrocytes encapsulated in GelMA for osteochondral tissue engineering.

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本文引用的文献

[1]
Osteochondral Fracture Fixation With Fragment Preserving Suture Technique.

Arthrosc Tech. 2020-6-15

[2]
Editorial Commentary: Aragonite-Based Implants for Osteochondral Defects-Could Coral Make Old Goats Run Again?

Arthroscopy. 2020-5-20

[3]
Reconstruction of Large Osteochondral Defects Using a Hemicondylar Aragonite-Based Implant in a Caprine Model.

Arthroscopy. 2020-7

[4]
Open Reduction, Bone Grafting, and Internal Fixation of Osteochondritis Dissecans Lesion of the Knee.

JBJS Essent Surg Tech. 2019-7-10

[5]
Articular cartilage regeneration: The role of endogenous mesenchymal stem/progenitor cell recruitment and migration.

Semin Arthritis Rheum. 2020-4

[6]
The Modified Hedgehog Technique to Repair Pure Chondral Shear-off Lesions in the Pediatric Knee.

Cartilage. 2021-12

[7]
Bioactive scaffolds for osteochondral regeneration.

J Orthop Translat. 2018-12-26

[8]
MaioRegen Osteochondral Substitute for the Treatment of Knee Defects: A Systematic Review of the Literature.

J Clin Med. 2019-6-1

[9]
Beyond Cartilage Repair: The Role of the Osteochondral Unit in Joint Health and Disease.

Tissue Eng Part B Rev. 2019-4

[10]
Agili-C implant promotes the regenerative capacity of articular cartilage defects in an ex vivo model.

Knee Surg Sports Traumatol Arthrosc. 2018-11-1

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