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Orchestrating osteogenic differentiation of mesenchymal stem cells - Identification of placental growth factor as a mechanosensitive gene with a pro-osteogenic role

机译:协调间充质干细胞的成骨分化-胎盘生长因子鉴定为具有促成骨作用的机械敏感基因

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Skeletogenesis is initiated during fetal development and persists through adult life as either a remodeling process in response to homeostatic regulation or as a regenerative process in response to physical injury. Mesenchymal stem cells (MSCs) play a crucial role providing progenitor cells from which osteoblasts, bone matrix forming cells are differentiated. The mechanical environment plays an important role in regulating stem cell differentiation into osteoblasts, however, the mechanisms by which MSCs respond to mechanical stimuli are yet to be fully elucidated. To increase understanding of MSC mechanotransuction and osteogenic differentiation, this study aimed to identify novel, mechanically augmented genes and pathways with pro-osteogenic functionality. Using collagen glycoaminoglycan scaffolds as mimics of native extracellular matrix, to create a 3D environment more representative of that found in bone, MSC-seeded constructs were mechanically stimulated in a flow-perfusion bioreactor. Global gene expression profiling techniques were used to identify potential candidates warranting further investigation. Of these, placental growth factor (PGF) was selected and expression levels were shown to strongly correlate to both the magnitude and duration of mechanical stimulation. We demonstrated that PGF gene expression was modulated through an actin polymerization-mediated mechanism. The functional role of PGF in modulating MSC osteogenic differentiation was interrogated, and we showed a concentration-dependent response whereby low concentrations exhibited the strongest pro-osteogenic effect. Furthermore, pre-osteoclast migration and differentiation, as well as endothelial cell tubule formation also maintained concentration-dependent responses to PGF, suggesting a potential role for PGF in bone resorption and angiogenesis, processes key to bone remodeling and fracture repair.
机译:骨骼生成是在胎儿发育过程中开始的,并在成年后持续存在,要么作为对稳态调节的响应的重塑过程,要么作为对身体伤害的响应的再生过程。间充质干细胞(MSC)发挥着至关重要的作用,可提供分化成骨细胞,骨基质形成细胞的祖细胞。机械环境在调节干细胞向成骨细胞的分化中起着重要作用,但是,MSC对机械刺激作出反应的机制尚未完全阐明。为了增加对MSC机械转位和成骨分化的了解,本研究旨在鉴定具有促成骨功能的新型,机械增强基因和途径。使用胶原蛋白糖胺聚糖支架作为天然细胞外基质的模拟物,以创建一个更能代表骨骼中存在的3D环境,在流动灌注生物反应器中对MSC接种的构建体进行机械刺激。全球基因表达谱分析技术被用于识别有待进一步研究的潜在候选基因。其中,选择胎盘生长因子(PGF)并显示其表达水平与机械刺激的大小和持续时间密切相关。我们证明了PGF基因表达是通过肌动蛋白聚合介导的机制进行调节的。询问了PGF在调节MSC成骨分化中的功能作用,并且我们显示了浓度依赖性反应,其中低浓度显示出最强的促成骨作用。此外,破骨细胞的迁移和分化以及内皮细胞小管的形成也维持了对PGF的浓度依赖性反应,表明PGF在骨吸收和血管生成,骨重塑和骨折修复的关键过程中具有潜在作用。

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