Anti-Inflammatory Performance of Lactose-Modified Chitosan and Hyaluronic Acid Mixtures in an In Vitro Macrophage-Mediated Inflammation Osteoarthritis Model.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
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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Auteurs

Elena Tarricone (E)

Department of Molecular Medicine, Histology Unit, University of Padova, 35121 Padova, Italy.

Elena Mattiuzzo (E)

Department of Molecular Medicine, Histology Unit, University of Padova, 35121 Padova, Italy.

Elisa Belluzzi (E)

Musculoskeletal Pathology and Oncology Laboratory, Orthopedic Clinic, Department of Surgery, Oncology and Gastroenterology, University of Padova, 35128 Padova, Italy.

Rossella Elia (R)

Department of Molecular Medicine, Histology Unit, University of Padova, 35121 Padova, Italy.

Andrea Benetti (A)

Department of Molecular Medicine, Histology Unit, University of Padova, 35121 Padova, Italy.

Rina Venerando (R)

Department of Molecular Medicine, University of Padova, 35121 Padova, Italy.

Vincenzo Vindigni (V)

Clinic of Plastic and Reconstructive Surgery, University of Padova, 35128 Padova, Italy.

Pietro Ruggieri (P)

Orthopedic Clinic, Department of Surgery, Oncology and Gastroenterology, University of Padova, 35128 Padova, Italy.

Paola Brun (P)

Department of Molecular Medicine, Histology Unit, University of Padova, 35121 Padova, Italy.

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Classifications MeSH