Institute of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof. Ernst Nathan Str. 1, 90419 Nuremberg, Germany.
Department of Biosciences, Paris Lodron University of Salzburg, Hellbrunnerstr. 34, 5020 Salzburg, Austria.
Int J Mol Sci. 2021 Jul 30;22(15):8204. doi: 10.3390/ijms22158204.
Anterior cruciate ligament (ACL) ruptures are usually treated with autograft implantation to prevent knee instability. Tissue engineered ACL reconstruction is becoming promising to circumvent autograft limitations. The aim was to evaluate the influence of cyclic stretch on lapine (L) ACL fibroblasts on embroidered scaffolds with respect to adhesion, DNA and sulphated glycosaminoglycan (sGAG) contents, gene expression of ligament-associated extracellular matrix genes, such as type I collagen, decorin, tenascin C, tenomodulin, gap junctional connexin 43 and the transcription factor Mohawk. Control scaffolds and those functionalized by gas phase fluorination and cross-linked collagen foam were either pre-cultured with a suspension or with spheroids of LACL cells before being subjected to cyclic stretch (4%, 0.11 Hz, 3 days). Stretch increased significantly the scaffold area colonized with cells but impaired sGAGs and decorin gene expression (functionalized scaffolds seeded with cell suspension). Stretching increased tenascin C, connexin 43 and Mohawk but decreased decorin gene expression (control scaffolds seeded with cell suspension). Pre-cultivation of functionalized scaffolds with spheroids might be the more suitable method for maintaining ligamentogenesis in 3D scaffolds compared to using a cell suspension due to a significantly higher sGAG content in response to stretching and type I collagen gene expression in functionalized scaffolds.
前交叉韧带(ACL)撕裂通常采用自体移植物植入物来治疗,以防止膝关节不稳定。组织工程 ACL 重建术有望避免自体移植物的局限性。目的是评估循环拉伸对兔 ACL 成纤维细胞在绣花支架上的影响,研究涉及粘附、DNA 和硫酸化糖胺聚糖(sGAG)含量、与韧带相关的细胞外基质基因的基因表达,如 I 型胶原、饰胶蛋白聚糖、腱糖蛋白 C、腱调蛋白、缝隙连接连接蛋白 43 和转录因子 Mohawk。对照支架和经气相氟化和交联胶原泡沫功能化的支架在进行循环拉伸(4%,0.11 Hz,3 天)之前,要么用细胞悬液预培养,要么用兔 ACL 细胞的球体预培养。拉伸显著增加了细胞定植的支架面积,但损害了 sGAG 和饰胶蛋白聚糖基因表达(用细胞悬液接种的功能化支架)。拉伸增加了腱糖蛋白 C、连接蛋白 43 和 Mohawk,但降低了饰胶蛋白聚糖基因表达(用细胞悬液接种的对照支架)。与使用细胞悬液相比,用球体预培养功能化支架可能是在 3D 支架中维持韧带形成的更合适的方法,因为在功能化支架中,拉伸时 sGAG 含量和 I 型胶原基因表达明显更高。