Kawaguchi N, Noda M
Department of Molecular Pharmacology, Medical Research Institute, Tokyo, Japan.
Exp Cell Res. 2000 Nov 1;260(2):284-91. doi: 10.1006/excr.2000.5020.
Microphthalmia mutant (mi/mi) mice reveal defects in osteoclastogenesis and exhibit osteopetrosis. However, there have been no studies to test the importance of Mitf in in vitro osteoclastogenesis using the cells derived from mi/mi mice. Therefore, we investigated in vitro osteoclastogenesis using the cells derived from mi/mi mice. We cocultured spleen cells prepared from either wild-type or mi/mi mice with ST2 or TM8 stromal cells and found that formation of TRAP-positive cells was significantly reduced in the cocultures of mi/mi spleen cells compared to wild-type spleen cells in the presence of 1,25(OH)(2) vitamin D(3) (vitamin D). We further investigated Mitf expression by Northern blot analysis in relation to the differentiation of osteoclasts using the cocultures of bone marrow cells with stromal/osteoblastic cells and found positive correlation in expression levels of c-fms and Mitf. Moreover, osteoclast-progenitor-like C7 cells expressed c-fms as well as Mitf mRNAs when cultured alone. C7 cells also expressed Mitf protein in their nuclei. Similar results were obtained when we used primary spleen cells, which differentiate into osteoclasts cultured in the presence of M-CSF and RANKL/ODF. Mitf expression levels in the cocultures of C7 cells and ST2 cells were not changed by treatment with vitamin D in the presence or absence of dexthamethasone. These results suggest that Mitf is expressed in osteoclast progenitors and its presence facilitates osteoclastogenesis.
小眼突变(mi/mi)小鼠表现出破骨细胞生成缺陷并呈现骨质石化。然而,尚未有研究使用来自mi/mi小鼠的细胞来测试小眼转录因子(Mitf)在体外破骨细胞生成中的重要性。因此,我们使用来自mi/mi小鼠的细胞研究了体外破骨细胞生成。我们将野生型或mi/mi小鼠制备的脾细胞与ST2或TM8基质细胞共培养,发现在存在1,25(OH)₂维生素D₃(维生素D)的情况下,与野生型脾细胞相比,mi/mi脾细胞共培养物中抗酒石酸酸性磷酸酶(TRAP)阳性细胞的形成显著减少。我们进一步通过Northern印迹分析研究了使用骨髓细胞与基质/成骨细胞共培养时Mitf表达与破骨细胞分化的关系,发现c-fms和Mitf的表达水平呈正相关。此外,破骨细胞祖细胞样C7细胞单独培养时表达c-fms以及Mitf mRNA。C7细胞在其细胞核中也表达Mitf蛋白。当我们使用在巨噬细胞集落刺激因子(M-CSF)和核因子κB受体活化因子配体/骨保护素配体(RANKL/ODF)存在下培养可分化为破骨细胞的原代脾细胞时,获得了类似的结果。在存在或不存在地塞米松的情况下,用维生素D处理不会改变C7细胞和ST2细胞共培养物中Mitf的表达水平。这些结果表明Mitf在破骨细胞祖细胞中表达,其存在促进破骨细胞生成。