Cargando…

Chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with M1 macrophages

BACKGROUND: Osteoarthritis (OA) is described by an imbalance between anabolic and catabolic processes in the affected joint. This dysregulation of metabolism affects not only chondrocytes within cartilage tissue but also the cells of the synovial membrane across the border of the joint. An important...

Descripción completa

Detalles Bibliográficos
Autores principales: Bauer, Christoph, Niculescu-Morzsa, Eugenia, Jeyakumar, Vivek, Kern, Daniela, Späth, Stephan S., Nehrer, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5020517/
https://www.ncbi.nlm.nih.gov/pubmed/27625590
http://dx.doi.org/10.1186/s12950-016-0139-y
_version_ 1782453218550218752
author Bauer, Christoph
Niculescu-Morzsa, Eugenia
Jeyakumar, Vivek
Kern, Daniela
Späth, Stephan S.
Nehrer, Stefan
author_facet Bauer, Christoph
Niculescu-Morzsa, Eugenia
Jeyakumar, Vivek
Kern, Daniela
Späth, Stephan S.
Nehrer, Stefan
author_sort Bauer, Christoph
collection PubMed
description BACKGROUND: Osteoarthritis (OA) is described by an imbalance between anabolic and catabolic processes in the affected joint. This dysregulation of metabolism affects not only chondrocytes within cartilage tissue but also the cells of the synovial membrane across the border of the joint. An important factor in OA is the low viscosity of the synovial fluid. High-molecular-weight hyaluronic acid (HA) can be used to increase the viscosity and also reduce inflammatory processes. The purpose was to establish an in vitro inflammation model and to evaluate the effects of high-molecular-weight HA in a co-cultivation inflammation model of osteoarthritic chondrocytes and M1 macrophages. METHODS: For the establishment of the inflammation model THP-1 cells were, at first, differentiated to M0 macrophages and then activated to the M1 subtype after 5 days of resting period. Surface markers, cytokine release, and gene expression, were analyzed to examine the successful differentiation. In the inflammation model, the defined M1 macrophages were co-cultivated with osteoarthritic chondrocytes for 2 days, with and without the addition of 10 % HA and further analyzed for chondrogenic gene expression markers and the release of cytokines in the supernatant. RESULTS: The differentiation and activation process was successful as M1 macrophages expressed higher levels of pro-inflammatory cytokines and specific genes. Similarly, the surface marker CD14 was significantly decreased compared to M0 macrophages. For the co-culture system, the analysis of gene expression showed that HA increased the expression of cartilage-specific genes while catabolic-encoding genes exhibited lower expression levels than the control group. This positive effect of HA was also demonstrated by the measurement of pro-inflammatory cytokines, as their level decreased. CONCLUSION: Our study implies that high-molecular-weight HA has a chondroprotective effect in the present co-cultivation inflammation model, as it decreases pro-inflammatory cytokines and increases anabolic factors.
format Online
Article
Text
id pubmed-5020517
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-50205172016-09-14 Chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with M1 macrophages Bauer, Christoph Niculescu-Morzsa, Eugenia Jeyakumar, Vivek Kern, Daniela Späth, Stephan S. Nehrer, Stefan J Inflamm (Lond) Research BACKGROUND: Osteoarthritis (OA) is described by an imbalance between anabolic and catabolic processes in the affected joint. This dysregulation of metabolism affects not only chondrocytes within cartilage tissue but also the cells of the synovial membrane across the border of the joint. An important factor in OA is the low viscosity of the synovial fluid. High-molecular-weight hyaluronic acid (HA) can be used to increase the viscosity and also reduce inflammatory processes. The purpose was to establish an in vitro inflammation model and to evaluate the effects of high-molecular-weight HA in a co-cultivation inflammation model of osteoarthritic chondrocytes and M1 macrophages. METHODS: For the establishment of the inflammation model THP-1 cells were, at first, differentiated to M0 macrophages and then activated to the M1 subtype after 5 days of resting period. Surface markers, cytokine release, and gene expression, were analyzed to examine the successful differentiation. In the inflammation model, the defined M1 macrophages were co-cultivated with osteoarthritic chondrocytes for 2 days, with and without the addition of 10 % HA and further analyzed for chondrogenic gene expression markers and the release of cytokines in the supernatant. RESULTS: The differentiation and activation process was successful as M1 macrophages expressed higher levels of pro-inflammatory cytokines and specific genes. Similarly, the surface marker CD14 was significantly decreased compared to M0 macrophages. For the co-culture system, the analysis of gene expression showed that HA increased the expression of cartilage-specific genes while catabolic-encoding genes exhibited lower expression levels than the control group. This positive effect of HA was also demonstrated by the measurement of pro-inflammatory cytokines, as their level decreased. CONCLUSION: Our study implies that high-molecular-weight HA has a chondroprotective effect in the present co-cultivation inflammation model, as it decreases pro-inflammatory cytokines and increases anabolic factors. BioMed Central 2016-09-13 /pmc/articles/PMC5020517/ /pubmed/27625590 http://dx.doi.org/10.1186/s12950-016-0139-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Bauer, Christoph
Niculescu-Morzsa, Eugenia
Jeyakumar, Vivek
Kern, Daniela
Späth, Stephan S.
Nehrer, Stefan
Chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with M1 macrophages
title Chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with M1 macrophages
title_full Chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with M1 macrophages
title_fullStr Chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with M1 macrophages
title_full_unstemmed Chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with M1 macrophages
title_short Chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with M1 macrophages
title_sort chondroprotective effect of high-molecular-weight hyaluronic acid on osteoarthritic chondrocytes in a co-cultivation inflammation model with m1 macrophages
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5020517/
https://www.ncbi.nlm.nih.gov/pubmed/27625590
http://dx.doi.org/10.1186/s12950-016-0139-y
work_keys_str_mv AT bauerchristoph chondroprotectiveeffectofhighmolecularweighthyaluronicacidonosteoarthriticchondrocytesinacocultivationinflammationmodelwithm1macrophages
AT niculescumorzsaeugenia chondroprotectiveeffectofhighmolecularweighthyaluronicacidonosteoarthriticchondrocytesinacocultivationinflammationmodelwithm1macrophages
AT jeyakumarvivek chondroprotectiveeffectofhighmolecularweighthyaluronicacidonosteoarthriticchondrocytesinacocultivationinflammationmodelwithm1macrophages
AT kerndaniela chondroprotectiveeffectofhighmolecularweighthyaluronicacidonosteoarthriticchondrocytesinacocultivationinflammationmodelwithm1macrophages
AT spathstephans chondroprotectiveeffectofhighmolecularweighthyaluronicacidonosteoarthriticchondrocytesinacocultivationinflammationmodelwithm1macrophages
AT nehrerstefan chondroprotectiveeffectofhighmolecularweighthyaluronicacidonosteoarthriticchondrocytesinacocultivationinflammationmodelwithm1macrophages