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首页> 外文期刊>Stem cells international >Beneficial Effects of Coculturing Synovial Derived Mesenchymal Stem Cells with Meniscus Fibrochondrocytes Are Mediated by Fibroblast Growth Factor 1: Increased Proliferation and Collagen Synthesis
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Beneficial Effects of Coculturing Synovial Derived Mesenchymal Stem Cells with Meniscus Fibrochondrocytes Are Mediated by Fibroblast Growth Factor 1: Increased Proliferation and Collagen Synthesis

机译:滑膜衍生间充质干细胞与半月板纤维软骨细胞共培养的有益作用是由成纤维细胞生长因子1介导的:增殖和胶原合成增加

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摘要

Meniscus reconstruction is in great need for orthopedic surgeons. Meniscal fibrochondrocytes transplantation was proposed to regenerate functional meniscus, with limited donor supply. We hypothesized that coculture of synovial mesenchymal stem cells (SSC) with meniscal fibrochondrocytes (me-CH) can support matrix production of me-CH, thus reducing the number of me-CH needed for meniscus reconstruction. A pellet coculture system of human SSC and me-CH was used in this study. Enhanced glycosaminoglycans (GAG) in coculture pellets were demonstrated by Alcian blue staining and GAG quantification, when compared to monoculture. More collagen synthesis was shown in coculture pellets by hydroxyproline assay. Increased proliferation of me-CH was observed in coculture. Data from BrdU staining and ELISA demonstrated that conditioned medium of SSCs enhanced the proliferation and collagen synthesis of me-CH, and this effect was blocked by neutralizing antibody against fibroblast growth factor 1 (FGF1). Western blot showed that conditioned medium of SSCs can activate mitogen-activated protein kinase (MAPK) signaling pathways by increasing the phosphorylation of mitogen-activated regulated protein kinase 1/2 (MEK) and extracellular-signal-regulated kinases 1/2 (ERK). Overall, this study provided evidence that synovial MSCs can support proliferation and collagen synthesis of fibrochondrocytes, by secreting FGF1. Coimplantation of SSC and me-CH could be a useful strategy for reconstructing meniscus.
机译:整形外科医师非常需要半月板重建。提出半月板纤维软骨细胞移植可再生功能性半月板,但供体供应有限。我们假设滑膜间充质干细胞(SSC)与半月板纤维软骨细胞(me-CH)的共培养可以支持me-CH的基质产生,从而减少了半月板重建所需的me-CH数量。在这项研究中使用了人类SSC和me-CH的颗粒共培养系统。与单培养相比,共培养沉淀中增强的糖胺聚糖(GAG)通过Alcian蓝染色和GAG定量证明。通过羟脯氨酸分析在共培养沉淀中显示更多的胶原蛋白合成。在共培养物中观察到me-CH的增殖增加。来自BrdU染色和ELISA的数据表明,SSC的条件培养基可增强me-CH的增殖和胶原蛋白合成,并且这种作用被中和抗成纤维细胞生长因子1(FGF1)的抗体所阻断。 Western印迹显示,SSC的条件培养基可以通过增加丝裂原激活的蛋白激酶1/2(MEK)和细胞外信号调节的激酶1/2(ERK)的磷酸化来激活丝裂原激活的蛋白激酶(MAPK)信号通路。 。总的来说,这项研究提供了证据,表明滑膜间充质干细胞可以通过分泌FGF1来支持纤维软骨细胞的增殖和胶原合成。 SSC和me-CH的共植入可能是重建半月板的有用策略。

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