首页> 外文期刊>Biological & pharmaceutical bulletin >Effect of Bone Morphogenetic Protein-2 (BMP-2) or Troglitazone, as an Inducer of Osteogenic Cells or Adipocytes, on Differentiation of a Bone Marrow Mesenchymal Progenitor Cell Line Established from Temperature-Sensitive (ts) Simian Virus (SV) 40 T-Antigen Gene Transgenic Mice
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Effect of Bone Morphogenetic Protein-2 (BMP-2) or Troglitazone, as an Inducer of Osteogenic Cells or Adipocytes, on Differentiation of a Bone Marrow Mesenchymal Progenitor Cell Line Established from Temperature-Sensitive (ts) Simian Virus (SV) 40 T-Antigen Gene Transgenic Mice

机译:成骨细胞或脂肪细胞诱导剂骨形态发生蛋白2(BMP-2)或曲格列酮对从温度敏感(ts)猿猴病毒(SV)40 T-建立的骨髓间充质祖细胞分化的影响抗原基因转基因小鼠

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摘要

TBR31-2 is one of the bone marrow stromal cell lines. Differentiation toward osteogenic cells and calcification was observed when TBR31-2 cells were cultured for 4 weeks. Bone morphogenetic protein-2 (BMP-2) stimulated alkaline phosphatase (ALP) activity in a dose- and time-dependent manner. On the other hand, troglitazone increased oil droplet accumulation in a dose-dependent manner. In the presence of BMP-2, an increase of expression in osteogenic cell differentiation marker genes and a decrease of expression in adipocyte differentiation marker genes were observed with the exception of the induced expression of peroxisome proliferator-activated receptor gamma (PPAR gamma), however, troglitazone, a ligand of PPAR gamma treatment exhibited the opposite tendency. Interestingly, treatment with both BMP-2 and troglitazone resulted in a decrease of ALP activity and an increase of oil droplet accumulation. Reverse tanscription-polymerase chain reaction (RT-PCR) analysis also indicated that osteogenic differentiation markers decreased and that adipocyte differentiation markers increased. Thus, when the cells were cultured with BMP-2, osteogenic differentiation was enhanced while the expression of PPAR gamma was maintained, and the addition of troglitazone caused a significant number of differentiated cells into adipocytes. These findings indicate that BMP-2 enhanced osteogenic differentiation and the expression of adipogenic transcription factor (PPAR gamma) followed by osteogenic differentiation without activation of PPAR gamma by its ligand.
机译:TBR31-2是骨髓基质细胞系之一。将TBR31-2细胞培养4周后,观察到了向成骨细胞的分化和钙化。骨形态发生蛋白2(BMP-2)以剂量和时间依赖性方式刺激了碱性磷酸酶(ALP)的活性。另一方面,曲格列酮以剂量依赖的方式增加了油滴的积累。在存在BMP-2的情况下,除了诱导的过氧化物酶体增殖物激活受体γ(PPARγ)的表达外,观察到成骨细胞分化标记基因表达的增加和脂肪细胞分化标记基因的表达的减少。 PPARγ处理的配体曲格列酮呈现相反的趋势。有趣的是,同时用BMP-2和曲格列酮治疗导致ALP活性降低和油滴积累增加。逆转录聚合酶链反应(RT-PCR)分析还表明成骨分化标志物减少,而脂肪细胞分化标志物增加。因此,当用BMP-2培养细胞时,在保持PPARγ的表达的同时,促进了成骨分化,并且曲格列酮的添加导致大量分化的细胞成为脂肪细胞。这些发现表明,BMP-2增强了成骨分化和成脂转录因子(PPARγ)的表达,随后在没有其配体激活PPARγ的情况下成骨分化。

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