Response of mature meniscal tissue to a single injurious compression and interleukin-1 in vitro

被引:10
|
作者
Hufeland, M. [1 ]
Schuenke, M. [1 ]
Grodzinsky, A. J. [2 ]
Imgenberg, J. [1 ]
Kurz, B. [3 ]
机构
[1] Univ Kiel, Inst Anat, D-24118 Kiel, Germany
[2] MIT, Cambridge, MA 02139 USA
[3] Bond Univ, Sch Med, Gold Coast, Qld 4229, Australia
关键词
Meniscus; Injury; Overload; Compression; Interleukin-1; In vitro; Cell viability; NECROSIS-FACTOR-ALPHA; HUMAN ARTICULAR-CARTILAGE; KNEE OSTEOARTHRITIS; DYNAMIC COMPRESSION; MECHANICAL INJURY; GENE-EXPRESSION; NITRIC-OXIDE; EXPLANTS; MENISCECTOMY; APOPTOSIS;
D O I
10.1016/j.joca.2012.10.003
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: To study mechanical overload of mature meniscal tissue under normal and pro-inflammatory conditions in vitro. Method: Three days after a single unconfined compression (strain: 25-75%, strain rate 1/s) of meniscal explants from 16 to 24 months-old cattle combined with interleukin-1-treatment (IL-1, 10 ng/ml) release of glycosaminoglycans (GAGs; dimethylmethylene blue (DMMB) assay), lactate dehydrogenase (LDH; cytotoxicity detection kit), and nitric oxide (NO; Griess assay), as well as gene transcription (quantitative reverse transcription polymerase chain reaction (RT-PCR)) and numbers of cells with condensed nuclei (CN; histomorphometry) were determined. Results: Mean peak stresses during compression were about five (25%), 11 (50%), and 30 MPa (75%), respectively. GAG and LDH release and numbers of CN increased whereas NO production and mRNA levels of matrix metalloproteinase (MMP)-2, -3 and a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS)-4 decreased strain-dependently after compression. IL-1 induced an increase in GAG and NO release as well as MMP-2, -3 and ADAMTS-4 levels, but had no impact on the LDH release and slightly increased numbers of CN. However, in combination with compression the tissue responses were reduced and LDH and CN levels were increased compared to IL-1 alone. Conclusion: Our data suggest that a single impact compression induces cell damage and release of GAG and reduces the NO production and transcription of certain matrix-degrading enzymes. It also reduces the capacity of meniscal tissue to respond to IL-1, which might be related to the cell damage and suggests that the compression-related GAG release might rather be the result of immediate extracellular matrix-damage than a cell-mediated event. This, however, needs to be confirmed in future studies. (C) 2012 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:209 / 216
页数:8
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