Anti-Inflammatory Performance of Lactose-Modified Chitosan and Hyaluronic Acid Mixtures in an In Vitro Macrophage-Mediated Inflammation Osteoarthritis Model.
Anti-Inflammatory Agents
/ pharmacology
Antigens, CD
/ metabolism
Antigens, Differentiation, Myelomonocytic
/ metabolism
Cell Survival
/ drug effects
Chitosan
/ pharmacology
Chondrocytes
/ drug effects
Culture Media, Conditioned
/ pharmacology
Down-Regulation
/ drug effects
Gene Expression Regulation
/ drug effects
Humans
Hyaluronic Acid
/ pharmacology
Inflammation
/ pathology
Inflammation Mediators
/ metabolism
Interleukin-1beta
/ metabolism
Lactose
/ chemistry
Macrophages
/ drug effects
Matrix Metalloproteinases
/ metabolism
Models, Biological
Monocytes
/ drug effects
Osteoarthritis
/ genetics
Reactive Oxygen Species
/ metabolism
U937 Cells
chitosan
chondrocyte
hyaluronic acid
inflammation
osteoarthritis
Journal
Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052
Informations de publication
Date de publication:
26 05 2020
26 05 2020
Historique:
received:
03
04
2020
revised:
17
05
2020
accepted:
19
05
2020
entrez:
30
5
2020
pubmed:
30
5
2020
medline:
6
3
2021
Statut:
epublish
Résumé
The development and progression of osteoarthritis (OA) is associated with macrophage-mediated inflammation that generates a broad spectrum of cytokines and reactive oxygen species (ROS). This study investigates the effects of mid-MW hyaluronic acid (HA) in combination with a lactose-modified chitosan (CTL), on pro-inflammatory molecules and metalloproteinases (MMPs) expression, using an in vitro model of macrophage-mediated inflammation. To assess chondrocyte response to HA and CTL in the presence of macrophage derived inflammatory mediators, cells were exposed to the conditioned medium (CM) of U937 activated monocytes and changes in cell viability, pro-inflammatory mediators and MMPs expression or ROS generation were analysed. CTL induced changes in chondrocyte viability that are reduced by the presence of HA. The CM of activated U937 monocytes (macrophages) significantly increased gene expression of pro-inflammatory molecules and MMPs and intracellular ROS generation in human chondrocyte cultures. HA, CTL and their combinations counteracted the oxidative damage and restored gene transcription for IL-1β, TNF-α, Gal-1, MMP-3 and MMP-13 to near baseline values. This study suggests that HA-CTL mixture attenuated macrophage-induced inflammation, inhibited MMPs expression and exhibited anti-oxidative effects. This evidence provides an initial step toward the development of an early stage OA therapeutic treatment.
Identifiants
pubmed: 32466461
pii: cells9061328
doi: 10.3390/cells9061328
pmc: PMC7349682
pii:
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Antigens, CD
0
Antigens, Differentiation, Myelomonocytic
0
CD68 antigen, human
0
Culture Media, Conditioned
0
IL1B protein, human
0
Inflammation Mediators
0
Interleukin-1beta
0
Reactive Oxygen Species
0
Hyaluronic Acid
9004-61-9
Chitosan
9012-76-4
Matrix Metalloproteinases
EC 3.4.24.-
Lactose
J2B2A4N98G
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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