Nishii Naomi, Arai Michitsugu, Yanai Nobuaki, Togari Akifumi, Nakabayashi Toshikatsu
First Department of Biochemistry, School of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya, Hyogo 663-8179, Japan.
Biol Pharm Bull. 2009 Jan;32(1):10-7. doi: 10.1248/bpb.32.10.
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 (PPARgamma), however, troglitazone, a ligand of PPARgamma 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 PPARgamma 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 (PPARgamma) followed by osteogenic differentiation without activation of PPARgamma by its ligand.
TBR31 - 2是骨髓基质细胞系之一。当TBR31 - 2细胞培养4周时,可观察到其向成骨细胞分化及钙化现象。骨形态发生蛋白-2(BMP - 2)以剂量和时间依赖性方式刺激碱性磷酸酶(ALP)活性。另一方面,曲格列酮以剂量依赖性方式增加油滴积累。在BMP - 2存在的情况下,除过氧化物酶体增殖物激活受体γ(PPARγ)诱导表达外,成骨细胞分化标志物基因表达增加,脂肪细胞分化标志物基因表达减少,然而,PPARγ配体曲格列酮处理则表现出相反趋势。有趣的是,BMP - 2和曲格列酮共同处理导致ALP活性降低和油滴积累增加。逆转录-聚合酶链反应(RT - PCR)分析也表明成骨分化标志物减少,脂肪细胞分化标志物增加。因此,当细胞用BMP - 2培养时,成骨分化增强,同时PPARγ表达得以维持,而添加曲格列酮会使大量分化细胞转变为脂肪细胞。这些发现表明,BMP - 2增强了成骨分化以及成脂转录因子(PPARγ)的表达,且PPARγ表达先于成骨分化,其配体未激活PPARγ。