Osteochondral fluid transport in an ex vivo system

被引:0
|
作者
Hislop, Brady David [1 ]
Mercer, Ara K. [2 ]
Whitley, Alexandria G. [3 ]
Myers, Erik P. [1 ]
Mackin, Marie [2 ]
Heveran, Chelsea M. [1 ]
June, Ronald K. [1 ,4 ,5 ]
机构
[1] Montana State Univ, Dept Mech & Ind Engn, Bozeman, MT USA
[2] Montana State Univ, Dept Chem & Biochem, Bozeman, MT USA
[3] Johns Hopkins Univ, Dept Neurosci, Baltimore, MD USA
[4] Montana State Univ, Dept Cell Biol & Neurosci, Bozeman, MT USA
[5] Univ Washington, Dept Orthopaed & Sports Med, Seattle, WA USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Bone-to-cartilage fluid transport; Cyclic compression; Mechanotransduction; Osteoarthritis; SUBCHONDRAL BONE PLATE; ARTICULAR-CARTILAGE; SOLUTE TRANSPORT; DIFFUSION; INTERFACE;
D O I
10.1016/j.joca.2024.02.946
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: Alterations to bone-to-cartilage fluid transport may contribute to the development of osteoarthritis (OA). Larger biological molecules in bone may transport from bone-to-cartilage ( e.g., insulin, 5 kDa). However, many questions remain about fluid transport between these tissues. The objectives of this study were to (1) test for diffusion of 3 kDa molecular tracers from bone-to-cartilage and (2) assess potential differences in bone-to-cartilage fluid transport between different loading conditions. Design: Osteochondral cores extracted from bovine femurs (N = 10 femurs, 10 cores/femur) were subjected to either no-load ( i.e., pure diffusion), pre-load only, or cyclic compression (5 +/- 2% or 10 +/- 2% strain) in a two-chamber bioreactor. The bone was placed into the bone compartment followed by a 3 kDa dextran tracer, and tracer concentrations in the cartilage compartment were measured every 5 min for 120 min. Tracer concentrations were analyzed for differences in beginning, peak, and equilibrium concentrations, loading effects, and time-to-peak tracer concentration. Results: Peak tracer concentration in the cartilage compartment was significantly higher compared to the beginning and equilibrium tracer concentrations. Cartilage-compartment tracer concentration and maximum fluorescent intensity were influenced by strain magnitude. No time-to-peak relationship was found between strain magnitudes and cartilage-compartment tracer concentration. Conclusion: This study shows that bone-to-cartilage fluid transport occurs with 3 kDa dextran molecules. These are larger molecules to move between bone and cartilage than previously reported. Further, these results demonstrate the potential impact of cyclic compression on osteochondral fluid transport. Determining the baseline osteochondral fluid transport in healthy tissues is crucial to elucidating the mechanisms OA pathology. (c) 2024 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:907 / 911
页数:5
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