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Use of FGF-2 and FGF-18 to direct bone marrow stromal stem cells to chondrogenic and osteogenic lineages.

机译:使用FGF-2和FGF-18将骨髓基质干细胞定向到成软骨和成骨细胞系。

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摘要

AIM: Intervertebral disc degeneration/low back pain is the number one global musculoskeletal condition in terms of disability and socioeconomic impact. MATERIALS & METHODS: Multipotent mesenchymal stem cells (MSCs) were cultured in micromass pellets ± FGF-2 or -18 up to 41 days, matrix components were immunolocalized and gene expression monitored by quantitative-reverse transcription PCR. RESULTS: Chondrogenesis occurred earlier in FGF-18 than FGF-2 cultures. Lower COL2A1, COL10A1 and ACAN expression by day 41 indicated a downregulation in chondrocyte hypertrophy. MEF2c, ALPL, were upregulated; calcium, decorin and biglycan, and 4C3 and 7D4 chondroitin sulphate sulfation motifs were evident in FGF-18 but not FGF-2 pellets. CONCLUSION: FGF-2 and -18 preconditioned MSCs produced cell lineages which promoted chondrogenesis and osteogenesis and may be useful in the production of MSC lineages suitable for repair of cartilaginous tissue defects.
机译:目的:就残疾和社会经济影响而言,椎间盘退变/下腰痛是全球第一的肌肉骨骼疾病。材料与方法:将多能间充质干细胞(MSCs)培养在微质量团块FGF-2或-18中培养41天,对基质成分进行免疫定位,并通过定量逆转录PCR监测基因表达。结果:软骨形成发生在FGF-18中比FGF-2培养物中更早。到第41天,较低的COL2A1,COL10A1和ACAN表达表明软骨细胞肥大的下调。 MEF2c,ALPL被上调;钙,除蛋白和双糖链蛋白,以及4C3和7D4硫酸软骨素的硫酸化基序在FGF-18中很明显,而在FGF-2沉淀中却没有。结论:FGF-2和-18预处理的MSC产生了促进软骨形成和成骨的细胞谱系,可用于生产适合修复软骨组织缺损的MSC谱系。

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