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

被引:44
作者
Bauer, Christoph [1 ]
Niculescu-Morzsa, Eugenia [1 ]
Jeyakumar, Vivek [1 ]
Kern, Daniela [1 ]
Spaeth, Stephan S. [1 ]
Nehrer, Stefan [1 ]
机构
[1] Danube Univ Krems, Dept Hlth Sci & Biomed, Ctr Regenerat Med & Orthoped, Dr Karl Dorrek Str 30, Krems, Austria
来源
JOURNAL OF INFLAMMATION-LONDON | 2016年 / 13卷
关键词
Inflammation; Hyaluronic acid; Chondrocytes; Macrophages; HUMAN ARTICULAR CHONDROCYTES; KNEE OSTEOARTHRITIS; OXIDATIVE STRESS; SYNOVIAL-FLUID; THP-1; CELLS; DIFFERENTIATION; MECHANISMS; CULTURE; INTERLEUKIN-6; EXPRESSION;
D O I
10.1186/s12950-016-0139-y
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
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.
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页数:9
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