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首页> 外文期刊>Stem cells and development >Comparative analysis of paracrine factor expression in human adult mesenchymal stem cells derived from bone marrow, adipose, and dermal tissue
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Comparative analysis of paracrine factor expression in human adult mesenchymal stem cells derived from bone marrow, adipose, and dermal tissue

机译:骨髓,脂肪和真皮组织中人成年间充质干细胞旁分泌因子表达的比较分析

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摘要

Human adult mesenchymal stem cells (MSCs) support the engineering of functional tissue constructs by secreting angiogenic and cytoprotective factors, which act in a paracrine fashion to influence cell survival and vascularization. MSCs have been isolated from many different tissue sources, but little is known about how paracrine factor secretion varies between different MSC populations. We evaluated paracrine factor expression patterns in MSCs isolated from adipose tissue (ASCs), bone marrow (BMSCs), and dermal tissues [dermal sheath cells (DSCs) and dermal papilla cells (DPCs)]. Specifically, mRNA expression analysis identified insulin-like growth factor-1 (IGF-1), vascular endothelial growth factor-D (VEGF-D), and interleukin-8 (IL-8) to be expressed at higher levels in ASCs compared with other MSC populations whereas VEGF-A, angiogenin, basic fibroblast growth factor (bFGF), and nerve growth factor (NGF) were expressed at comparable levels among the MSC populations examined. Analysis of conditioned media (CM) protein confirmed the comparable level of angiogenin and VEGF-A secretion in all MSC populations and showed that DSCs and DPCs produced significantly higher concentrations of leptin. Functional assays examining in vitro angiogenic paracrine activity showed that incubation of endothelial cells in ASC CM resulted in increased tubulogenic efficiency compared with that observed in DPC CM. Using neutralizing antibodies we concluded that VEGF-A and VEGF-D were 2 of the major growth factors secreted by ASCs that supported endothelial tubulogenesis. The variation in paracrine factors of different MSC populations contributes to different levels of angiogenic activity and ASCs maybe preferred over other MSC populations for augmenting therapeutic approaches dependent upon angiogenesis.
机译:人类成人间充质干细胞(MSC)通过分泌血管生成和细胞保护因子来支持功能组织构建体的工程化,这些因子以旁分泌的方式起作用,从而影响细胞存活和血管形成。已从许多不同的组织来源中分离出MSC,但对不同MSC群体之间旁分泌因子分泌的变化知之甚少。我们评估了从脂肪组织(ASC),骨髓(BMSC)和真皮组织[真皮鞘细胞(DSC)和真皮乳头细胞(DPC)]分离的MSC中旁分泌因子的表达模式。具体来说,mRNA表达分析确定胰岛素样生长因子-1(IGF-1),血管内皮生长因子D(VEGF-D)和白介素8(IL-8)在ASC中的表达水平高于在其他MSC人群中,VEGF-A,血管生成素,碱性成纤维细胞生长因子(bFGF)和神经生长因子(NGF)的表达水平与所研究的MSC人群相当。条件培养基(CM)蛋白的分析证实了在所有MSC群体中血管生成素和VEGF-A分泌水平相当,并且表明DSC和DPC产生的瘦素浓度明显更高。检验体外血管生成旁分泌活性的功能分析表明,与DPC CM中观察到的相比,在ASC CM中孵育内皮细胞可提高肾小管生成效率。使用中和抗体,我们得出结论,VEGF-A和VEGF-D是ASC分泌的两个主要生长因子中的2个,这些生长因子支持内皮管的生成。不同MSC群体旁分泌因子的变化导致不同水平的血管生成活性,并且ASC可能优于其他MSC群体,以增强依赖于血管生成的治疗方法。

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