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维甲酸对 ST2 细胞(一种鼠骨髓基质细胞系)中脂肪细胞向成骨细胞倾向分化的逆转作用。

The effects of retinoic acid on reversing the adipocyte differentiation into an osteoblastic tendency in ST2 cells, a murine bone marrow-derived stromal cell line.

机构信息

Department of Bioengeneering, Tokyo Institute of Technology, 4259 Nagatsuta-cho, Midori-ku, Yokohama, 226-8501, Japan.

出版信息

Cytotechnology. 2001 Jul;36(1-3):125-36. doi: 10.1023/A:1014056012278.

Abstract

Although the mouse bone marrow stromal cell line ST2 has been known to be differentiated into osteoblasts, the differentiation characteristics of the cell into adipocyte and the concerned relationship between its adipogenesis and osteogenesis remains unknown. The adipogenic induction medium which is made up of insulin, dexamethasone (DEX) and 3-isobutyl-1-methylxanthine(IBMX), stimulated the expression of n early adipogenic marker PPAR gamma and a late marker GPDH in ST2 cells. The triglyceride accumulation and lipid stain level generated by the induction medium in ST2 cells was inhibited by RA with IC(50) at about 1 nM. The induction medium up-regulated expression of PPARgamma and GPDH was also inhibited by RA whereas RA (30 nM) exterted no effect on the cell growth. Interestingly, treatment of the cells with induction medium in the presense of RA caused a 3- or 10-fold higher in ALP activity respectively as compared to those treated with RA or the induction medium alone. RT-PCR analysis showed that such a synergistic effect of RA and the induction medium paralleled the process of inhibition on adipogenesis. Additional experiments showed that IBMX played a key role in increasing the effect of RA and ALP activity. Our results suggested that the relationship between adipogenesis and osteogenesis in ST2 cells was reciprocally interrelated and the process of adipogenesis could be potentially reversed into an osteoblastogenic tendency. This is the first report demonstrating that RA transforms adipogenic potential into an osteoblastic tendency.

摘要

虽然鼠骨髓基质细胞系 ST2 已知可分化为成骨细胞,但该细胞向脂肪细胞的分化特征及其成脂作用与成骨作用之间的关系尚不清楚。由胰岛素、地塞米松 (DEX) 和 3-异丁基-1-甲基黄嘌呤 (IBMX) 组成的成脂诱导培养基刺激 ST2 细胞中早期成脂标志物 PPARγ和晚期标志物 GPDH 的表达。RA(IC50 约为 1 nM)抑制诱导培养基在 ST2 细胞中产生的甘油三酯积累和脂质染色水平。RA 还抑制诱导培养基上调的 PPARγ和 GPDH 的表达,而 RA(30 nM)对细胞生长没有影响。有趣的是,与单独用 RA 或诱导培养基处理的细胞相比,RA 存在下用诱导培养基处理细胞可分别使 ALP 活性提高 3 倍或 10 倍。RT-PCR 分析表明,RA 和诱导培养基的这种协同作用与抑制成脂作用的过程平行。进一步的实验表明,IBMX 在增强 RA 的作用和 ALP 活性方面起着关键作用。我们的研究结果表明,ST2 细胞中脂肪生成和骨生成之间的关系是相互关联的,脂肪生成过程可能被潜在地逆转为成骨细胞样趋势。这是首次报道表明 RA 将成脂潜能转化为成骨细胞样趋势。

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