Cargando…

Inflammation-Modulating Hydrogels for Osteoarthritis Cartilage Tissue Engineering

Osteoarthritis (OA) is the most common form of the joint disease associated with age, obesity, and traumatic injury. It is a disabling degenerative disease that affects synovial joints and leads to cartilage deterioration. Despite the prevalence of this disease, the understanding of OA pathophysiolo...

Descripción completa

Detalles Bibliográficos
Autores principales: Koh, Rachel H., Jin, Yinji, Kim, Jisoo, Hwang, Nathaniel S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072320/
https://www.ncbi.nlm.nih.gov/pubmed/32059502
http://dx.doi.org/10.3390/cells9020419
_version_ 1783506379143643136
author Koh, Rachel H.
Jin, Yinji
Kim, Jisoo
Hwang, Nathaniel S.
author_facet Koh, Rachel H.
Jin, Yinji
Kim, Jisoo
Hwang, Nathaniel S.
author_sort Koh, Rachel H.
collection PubMed
description Osteoarthritis (OA) is the most common form of the joint disease associated with age, obesity, and traumatic injury. It is a disabling degenerative disease that affects synovial joints and leads to cartilage deterioration. Despite the prevalence of this disease, the understanding of OA pathophysiology is still incomplete. However, the onset and progression of OA are heavily associated with the inflammation of the joint. Therefore, studies on OA treatment have sought to intra-articularly deliver anti-inflammatory drugs, proteins, genes, or cells to locally control inflammation in OA joints. These therapeutics have been delivered alone or increasingly, in delivery vehicles for sustained release. The use of hydrogels in OA treatment can extend beyond the delivery of anti-inflammatory components to have inherent immunomodulatory function via regulating immune cell polarization and activity. Currently, such immunomodulatory biomaterials are being developed for other applications, which can be translated into OA therapy. Moreover, anabolic and proliferative levels of OA chondrocytes are low, except initially, when chondrocytes temporarily increase anabolism and proliferation in response to structural changes in their extracellular environment. Therefore, treatments need to restore matrix protein synthesis and proliferation to healthy levels to reverse OA-induced damage. In conjugation with injectable and/or adhesive hydrogels that promote cartilage tissue regeneration, immunomodulatory tissue engineering solutions will have robust potential in OA treatment. This review describes the disease, its current and future immunomodulatory therapies as well as cartilage-regenerative injectable and adhesive hydrogels.
format Online
Article
Text
id pubmed-7072320
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-70723202020-03-19 Inflammation-Modulating Hydrogels for Osteoarthritis Cartilage Tissue Engineering Koh, Rachel H. Jin, Yinji Kim, Jisoo Hwang, Nathaniel S. Cells Review Osteoarthritis (OA) is the most common form of the joint disease associated with age, obesity, and traumatic injury. It is a disabling degenerative disease that affects synovial joints and leads to cartilage deterioration. Despite the prevalence of this disease, the understanding of OA pathophysiology is still incomplete. However, the onset and progression of OA are heavily associated with the inflammation of the joint. Therefore, studies on OA treatment have sought to intra-articularly deliver anti-inflammatory drugs, proteins, genes, or cells to locally control inflammation in OA joints. These therapeutics have been delivered alone or increasingly, in delivery vehicles for sustained release. The use of hydrogels in OA treatment can extend beyond the delivery of anti-inflammatory components to have inherent immunomodulatory function via regulating immune cell polarization and activity. Currently, such immunomodulatory biomaterials are being developed for other applications, which can be translated into OA therapy. Moreover, anabolic and proliferative levels of OA chondrocytes are low, except initially, when chondrocytes temporarily increase anabolism and proliferation in response to structural changes in their extracellular environment. Therefore, treatments need to restore matrix protein synthesis and proliferation to healthy levels to reverse OA-induced damage. In conjugation with injectable and/or adhesive hydrogels that promote cartilage tissue regeneration, immunomodulatory tissue engineering solutions will have robust potential in OA treatment. This review describes the disease, its current and future immunomodulatory therapies as well as cartilage-regenerative injectable and adhesive hydrogels. MDPI 2020-02-12 /pmc/articles/PMC7072320/ /pubmed/32059502 http://dx.doi.org/10.3390/cells9020419 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Koh, Rachel H.
Jin, Yinji
Kim, Jisoo
Hwang, Nathaniel S.
Inflammation-Modulating Hydrogels for Osteoarthritis Cartilage Tissue Engineering
title Inflammation-Modulating Hydrogels for Osteoarthritis Cartilage Tissue Engineering
title_full Inflammation-Modulating Hydrogels for Osteoarthritis Cartilage Tissue Engineering
title_fullStr Inflammation-Modulating Hydrogels for Osteoarthritis Cartilage Tissue Engineering
title_full_unstemmed Inflammation-Modulating Hydrogels for Osteoarthritis Cartilage Tissue Engineering
title_short Inflammation-Modulating Hydrogels for Osteoarthritis Cartilage Tissue Engineering
title_sort inflammation-modulating hydrogels for osteoarthritis cartilage tissue engineering
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072320/
https://www.ncbi.nlm.nih.gov/pubmed/32059502
http://dx.doi.org/10.3390/cells9020419
work_keys_str_mv AT kohrachelh inflammationmodulatinghydrogelsforosteoarthritiscartilagetissueengineering
AT jinyinji inflammationmodulatinghydrogelsforosteoarthritiscartilagetissueengineering
AT kimjisoo inflammationmodulatinghydrogelsforosteoarthritiscartilagetissueengineering
AT hwangnathaniels inflammationmodulatinghydrogelsforosteoarthritiscartilagetissueengineering