首页> 外文期刊>Journal of cellular and molecular medicine. >Functional differences of Toll-like receptor 4 in osteogenesis, adipogenesis and chondrogenesis in human bone marrow-derived mesenchymal stem cells
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Functional differences of Toll-like receptor 4 in osteogenesis, adipogenesis and chondrogenesis in human bone marrow-derived mesenchymal stem cells

机译:人骨髓源性间充质干细胞骨质发生,脂肪发生和软骨发生中的收缩受体4的功能差异

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Multipotent human bone marrow-derived mesenchymal stem cells (hMSCs) are promising candidates for bone and cartilage regeneration. Toll-like receptor 4 (TLR4) is expressed by hMSCs and is a receptor for both exogenous and endogenous danger signals. TLRs have been shown to possess functional differences based on the species (human or mouse) they are isolated from therefore, the effects of knockdown of TLR4 were evaluated in humans during the differentiation of MSCs into bone, fat and chondrocyte cells in vitro. We investigated the expression profile of TLR4 during the differentiation of hMSCs into three different lineages on days 7, 14 and 21 and assessed the differentiation potential of the cells in the presence of lipopolysaccharide (LPS, as an exogenous agonist) and fibronectin fragment III-1c (FnIII-1c, as an endogenous agonist). TLR4 expression increased following the induction of hMSC differentiation into all three lineages. Alkaline phosphatase activity revealed that FnIII-1c accelerated calcium deposition on day 7, whereas LPS increased calcium deposition on day 14. Chondrogenesis increased in the presence of LPS; however, FnIII-1c acted as a reducer in the late stage. TLR4 silencing led to decreased osteogenesis and increased adipogenesis. Furthermore, Wnt5a expression was inversely related to chondrogenesis during the late stage of differentiation. We suggest that understanding the functionality of TLR4 (in the presence of pathogen or stress signal) during the differentiation of hMSCs into three lineages would be useful for MSC-based treatments.
机译:多能人骨髓衍生的间充质干细胞(HMSCs)是骨和软骨再生的候选者。 Toll样受体4(TLR4)由HMSCs表示,并且是外源性和内源性危险信号的受体。已经证明TLRS基于它们的物种(人或小鼠)具有从它们中分离的物种(人或小鼠)具有功能差异,在体外将MSC分化为骨,脂肪和软骨细胞细胞的人类中评估TLR4敲低的影响。我们在第7,14和21天将HMSC分化为三种不同谱系中TLR4的表达谱,并评估了在脂多糖(LPS,作为外源激动剂)和纤连蛋白片段III-1C的存在下细胞的分化电位(FNIII-1C,作为内源激动剂)。在诱导HMSC差异分析到所有三个谱系之后,TLR4表达增加。碱性磷酸酶活性显示,在第7天,FNIII-1C加速钙沉积,而LPS在第14天增加钙沉积。在LPS存在下,软骨发生增加;然而,FNIII-1C在晚期的减速器担任减速剂。 TLR4沉默导致成骨发生降低和增加的脂肪发生。此外,Wnt5a表达在分化后期期间与软骨发生相反。我们建议理解在HMSC分化到三个谱系中的TLR4(在病原体或应力信号存在下)的功能对于基于MSC的处理是有用的。

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