Regenerative Engineering Laboratory, Columbia University Irving Medical Center, 630 W. 168 St. - VC12-230, New York 10032, New York.
Department of Biomedical Engineering, The Pennsylvania State University, 205 Hallowell Building, University Park 16802-4400, Pennsylvania.
J Orthop Res. 2019 Jul;37(7):1555-1562. doi: 10.1002/jor.24287. Epub 2019 Mar 28.
Meniscus tears in the avascular region rarely functionally heal due to poor intrinsic healing capacity, frequently resulting in tear propagation, followed by meniscus deterioration. Recently, we have reported that time-controlled application of connective tissue growth factor (CTGF) and transforming tissue growth factor β3 (TGFβ3) significantly improved healing of avascular meniscus tears by inducing recruitment and step-wise fibrocartilaginous differentiation of mesenchymal stem/progenitor cells (MSCs). In this study, we investigated effects of the dose of CTGF and the release rate of TGFβ3 on avascular meniscus healing in our existing explant model. Our hypothesis was that dose and release rate of CTGF and TGFβ3 are contributing factors for functional outcome in avascular meniscus healing by stem cell recruitment. Low (100 ng/ml) and high (1,000 ng/ml) doses of CTGF as well as fast (0.46 ± 0.2 ng/day) and slow (0.29 ± 0.1 ng/day) release rates of TGFβ3 were applied to our established meniscus explant model for meniscus tears in the inner-third avascular region. The release rate of TGFβ3 was controlled by varying compositions of poly(lactic-co-glycolic acids) (PLGA) microspheres. The meniscus explants were then cultured for 8 weeks on top of mesenchymal stem/progenitor cells (MSCs). Among the tested combinations, we found that a high CTGF dose and slow TGFβ3 release are most effective for integrated healing of avascular meniscus, demonstrating improvements in alignment of collagen fibers, fibrocartilaginous matrix elaboration and mechanical properties. This study may represent an important step toward the development of a regenerative therapy to improve healing of avascular meniscus tears by stem cell recruitment. © 2019 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 37:1555-1562, 2019.
半月板在无血管区的撕裂很少能因内在愈合能力差而实现功能性愈合,通常会导致撕裂的扩展,进而导致半月板的恶化。最近,我们报告称,通过诱导间充质干细胞/祖细胞(MSCs)募集和逐步纤维软骨分化,时间控制给予结缔组织生长因子(CTGF)和转化生长因子β3(TGFβ3)可显著改善无血管半月板撕裂的愈合。在这项研究中,我们研究了 CTGF 的剂量和 TGFβ3 的释放率对我们现有的半月板外植体模型中无血管半月板愈合的影响。我们的假设是,CTGF 和 TGFβ3 的剂量和释放率是通过干细胞募集来改善无血管半月板愈合的功能结果的一个影响因素。我们将低(100ng/ml)和高(1000ng/ml)剂量的 CTGF 以及快(0.46±0.2ng/天)和慢(0.29±0.1ng/天)的 TGFβ3 释放率应用于我们建立的内侧三分之一无血管区半月板撕裂的半月板外植体模型。通过改变聚乳酸-共-羟基乙酸(PLGA)微球的组成来控制 TGFβ3 的释放率。然后将半月板外植体在间充质干细胞/祖细胞(MSCs)上培养 8 周。在测试的组合中,我们发现高 CTGF 剂量和慢 TGFβ3 释放对无血管半月板的综合愈合最有效,表现为胶原纤维排列、纤维软骨基质的产生和机械性能的改善。这项研究可能是开发通过干细胞募集来改善无血管半月板撕裂愈合的再生治疗的重要一步。©2019 骨科研究协会。由 Wiley Periodicals, Inc. 出版。J Orthop Res 37:1555-1562, 2019.