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Tendon and Cytokine Marker Expression by Human Bone Marrow Mesenchymal Stem Cells in a Hyaluronate/Poly-Lactic-Co-Glycolic Acid (PLGA)/Fibrin Three-Dimensional (3D) Scaffold

机译:透明质酸/聚乳酸-共乙醇酸(PLGA)/纤维蛋白三维(3D)支架中人骨髓间充质干细胞的肌腱和细胞因子标记表达。

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摘要

We developed a (three-dimensional) 3D scaffold, we named HY-FIB, incorporating a force-transmission band of braided hyaluronate embedded in a cell localizing fibrin hydrogel and poly-lactic-co-glycolic acid (PLGA) nanocarriers as transient components for growth factor controlled delivery. The tenogenic supporting capacity of HY-FIB on human-Bone Marrow Mesenchymal Stem Cells (hBM-MSCs) was explored under static conditions and under bioreactor-induced cyclic strain conditions. HY-FIB elasticity enabled to deliver a mean shear stress of 0.09 Pa for 4 h/day. Tendon and cytokine marker expression by hBM-MSCs were studied. Results: hBM-MSCs embedded in HY-FIB and subjected to mechanical stimulation, resulted in a typical tenogenic phenotype, as indicated by type 1 Collagen fiber immunofluorescence. RT-qPCR showed an increase of type 1 Collagen, scleraxis, and decorin gene expression (3-fold, 1600-fold, and 3-fold, respectively, at day 11) in dynamic conditions. Cells also showed pro-inflammatory (IL-6, TNF, IL-12A, IL-1β) and anti-inflammatory (IL-10, TGF-β1) cytokine gene expressions, with a significant increase of anti-inflammatory cytokines in dynamic conditions (IL-10 and TGF-β1 300-fold and 4-fold, respectively, at day 11). Mechanical signaling, conveyed by HY-FIB to hBM-MSCs, promoted tenogenic gene markers expression and a pro-repair cytokine balance. The results provide strong evidence in support of the HY-FIB system and its interaction with cells and its potential for use as a predictive in vitro model.
机译:我们开发了一种3D三维支架,命名为HY-FIB,它结合了透明质酸编织力传递带,该传递带嵌入细胞局部纤维蛋白水凝胶和聚乳酸-乙醇酸(PLGA)纳米载体中,作为瞬时成分生长因子控制的传递。在静态条件下和在生物反应器诱导的循环应变条件下,探索了HY-FIB对人骨髓间充质干细胞(hBM-MSC)的张力支持能力。 HY-FIB弹性能够在4小时/天的时间内提供0.09 Pa的平均剪切应力。研究了hBM-MSCs的肌腱和细胞因子标志物的表达。结果:嵌入HY-FIB并受到机械刺激的hBM-MSC产生典型的肌腱表型,如1型胶原纤维免疫荧光所示。 RT-qPCR显示在动态条件下1型胶原蛋白,硬化和除芯蛋白基因表达增加(在第11天分别为3倍,1600倍和3倍)。细胞还显示促炎性(IL-6,TNF,IL-12A,IL-1β)和抗炎性(IL-10,TGF-β1)细胞因子基因表达,在动态条件下抗炎性细胞因子显着增加(在第11天,IL-10和TGF-β1分别为300倍和4倍)。 HY-FIB传递给hBM-MSC的机械信号传递促进了肌腱基因标记的表达和促修复细胞因子的平衡。这些结果提供了有力的证据来支持HY-FIB系统及其与细胞的相互作用,并有可能用作体外预测模型。

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