Ling Carrie H-Y, Lai Janice H, Wong Ivan J, Levenston Marc E
Department of Mechanical Engineering, Stanford University, Stanford, California, 94305-4038.
J Orthop Res. 2016 May;34(5):801-11. doi: 10.1002/jor.23096. Epub 2015 Nov 25.
Despite increasing evidence that meniscal degeneration is an early event in the development of knee osteoarthritis, relatively little is known regarding the sequence or functional implications of cytokine-induced meniscal degradation or how degradation varies with age. This study examined dose-dependent patterns of interleukin-1 (IL-1)-induced matrix degradation in explants from the radially middle regions of juvenile and adult bovine menisci. Tissue explants were cultured for 10 days in the presence of 0, 1.25, 5, or 20 ng/ml recombinant human IL-1α. Juvenile explants exhibited immediate and extensive sulfated glycosaminoglycan (sGAG) loss and subsequent collagen release beginning after 4-6 days, with relatively little IL-1 dose-dependence. Adult explants exhibited a more graded response to IL-1, with dose-dependent sGAG release and a lower fraction of sGAG released (but greater absolute release) than juvenile explants. In contrast to juvenile explants, adult explants exhibited minimal collagen release over the 10-day culture. Compressive and shear moduli reflected the changes in explant composition, with substantial decreases for both ages but a greater relative decrease in juvenile tissue. Dynamic moduli exhibited stronger dependence on explant sGAG content for juvenile tissue, likely reflecting concomitant changes to both proteoglycan and collagen tissue components. The patterns of tissue degradation suggest that, like in articular cartilage, meniscal proteoglycans may partially protect collagen from cell-mediated degeneration. A more detailed view of functional changes in meniscal tissue mechanics with degeneration will help to establish the relevance of in vitro culture models and will advance understanding of how meniscal degeneration contributes to overall joint changes in early stage osteoarthritis. © 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:801-811, 2016.
尽管越来越多的证据表明半月板退变是膝关节骨关节炎发展过程中的早期事件,但对于细胞因子诱导的半月板降解的顺序或功能影响,以及降解如何随年龄变化,人们了解得相对较少。本研究检测了白细胞介素-1(IL-1)诱导的幼年和成年牛半月板径向中部区域外植体基质降解的剂量依赖性模式。将组织外植体在0、1.25、5或20 ng/ml重组人IL-1α存在的情况下培养10天。幼年外植体在4-6天后立即出现广泛的硫酸化糖胺聚糖(sGAG)丢失,随后胶原蛋白释放,且IL-1剂量依赖性相对较小。成年外植体对IL-1的反应更为分级,sGAG释放呈剂量依赖性,且释放的sGAG比例低于幼年外植体(但绝对释放量更大)。与幼年外植体不同,成年外植体在10天培养期间胶原蛋白释放极少。压缩模量和剪切模量反映了外植体成分的变化,两个年龄段的模量均大幅下降,但幼年组织的相对下降幅度更大。动态模量对幼年组织外植体sGAG含量的依赖性更强,这可能反映了蛋白聚糖和胶原组织成分的伴随变化。组织降解模式表明,与关节软骨一样,半月板蛋白聚糖可能部分保护胶原蛋白免受细胞介导的退变。对半月板组织力学功能变化与退变的更详细了解将有助于确定体外培养模型的相关性,并将促进对半月板退变如何导致早期骨关节炎整体关节变化的理解。©2015骨科学研究协会。由威利期刊公司出版。《矫形外科学研究》34:801-811,2016年。