Takagi Katsuhisa, Kudo Akira
Department of Biological Information, Tokyo Institute of Technology, 4259-B-33 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.
J Bone Miner Metab. 2008;26(1):13-23. doi: 10.1007/s00774-007-0787-3. Epub 2008 Jan 10.
Bone marrow stromal cells support osteoclast differentiation by expressing receptor activator of NF-kB ligand (RANKL). Although several bone marrow stromal cell lines have been established and characterized, the differentiation stage of the supporting cells for osteoclast differentiation remains unclear. We have established several bone marrow stromal cell lines from transgenic mice harboring the temperature-sensitive SV40 large T antigen. Some of these temperature-sensitive bone marrow stromal cell lines (TSB cell lines) support osteoclast differentiation and differentiate into osteoblasts, suggesting that osteoblast precursor cells support osteoclast differentiation. Here we show that the TSB cell lines that support osteoclast differentiation also expressed peroxisome proliferator-activated receptor gamma1 (PPARgamma1) and were able to differentiate into adipocytes. PPARgamma1 is an alternatively spliced form of PPARgamma that is responsible for the adipocyte differentiation and expressed in the adipocyte precursor cells. Immunofluorescence analysis of TSB cell lines and primary bone marrow stromal cells by use of anti-PPARgamma and anti-RANKL antibodies showed that fluorescent signals for RANKL were observed in the cells that expressed PPARgamma. Furthermore, activation of adipocyte differentiation by a PPARgamma agonist led to decreased RANKL expression. These results demonstrate that PPARgamma1-positive precursor cells for osteoblasts and adipocytes expressed RANKL and supported osteoclastogenesis.
骨髓基质细胞通过表达核因子κB受体激活蛋白配体(RANKL)来支持破骨细胞分化。尽管已经建立并鉴定了几种骨髓基质细胞系,但破骨细胞分化的支持细胞的分化阶段仍不清楚。我们从携带温度敏感型SV40大T抗原的转基因小鼠中建立了几种骨髓基质细胞系。其中一些温度敏感型骨髓基质细胞系(TSB细胞系)支持破骨细胞分化并分化为成骨细胞,这表明成骨细胞前体细胞支持破骨细胞分化。在此我们表明,支持破骨细胞分化的TSB细胞系也表达过氧化物酶体增殖物激活受体γ1(PPARγ1),并且能够分化为脂肪细胞。PPARγ1是PPARγ的一种可变剪接形式,负责脂肪细胞分化并在脂肪细胞前体细胞中表达。使用抗PPARγ和抗RANKL抗体对TSB细胞系和原代骨髓基质细胞进行免疫荧光分析表明,在表达PPARγ的细胞中观察到RANKL的荧光信号。此外,PPARγ激动剂激活脂肪细胞分化导致RANKL表达降低。这些结果表明,成骨细胞和脂肪细胞的PPARγ1阳性前体细胞表达RANKL并支持破骨细胞生成。