Lammi Johanna, Aarnisalo Piia
Institute of Biomedicine/Physiology, Biomedicum Helsinki, University of Helsinki, P.O. Box 63, FIN-00014 Helsinki, Finland.
Mol Cell Endocrinol. 2008 Nov 25;295(1-2):87-93. doi: 10.1016/j.mce.2008.08.023. Epub 2008 Sep 3.
Nurr1, NGFI-B, and Nor1 form the NR4A subfamily of orphan nuclear receptors. The NR4A receptors are immediate early genes that can be rapidly induced in response to a variety of stimuli in many cell types, for example, in osteoblasts. Nurr1 regulates the differentiation of osteoblasts and the expression of several osteoblastic genes. Fibroblast growth factor 8b (FGF-8b) regulates osteoblastic differentiation. We show here that treatment of preosteoblastic MC3T3-E1 cells or mouse bone marrow mesenchymal cells with FGF-8b induces the expression of NR4A receptors rapidly and in a dose-dependent manner. This induction involves mitogen-activated protein kinase (MAPK), phosphatidylinositol-3-kinase (PI-3K), and protein kinase C (PKC) pathways. FGF-8b stimulates the proliferation of MC3T3-E1 cells. This effect is enhanced by overexpression of Nurr1 and NGFI-B whereas it is abolished by a dominant negative Nurr1 variant. In conclusion, FGF-8b induces the expression of NR4A orphan nuclear receptors that are involved in mediating the growth promoting effect of FGF-8b in osteoblasts.
Nurr1、NGFI-B和Nor1构成孤儿核受体的NR4A亚家族。NR4A受体是即刻早期基因,在许多细胞类型中,例如在成骨细胞中,可对多种刺激迅速做出反应而被诱导表达。Nurr1调节成骨细胞的分化以及几种成骨细胞基因的表达。成纤维细胞生长因子8b(FGF-8b)调节成骨细胞分化。我们在此表明,用FGF-8b处理前成骨细胞MC3T3-E1细胞或小鼠骨髓间充质细胞可迅速且以剂量依赖的方式诱导NR4A受体的表达。这种诱导涉及丝裂原活化蛋白激酶(MAPK)、磷脂酰肌醇-3-激酶(PI-3K)和蛋白激酶C(PKC)途径。FGF-8b刺激MC3T3-E1细胞的增殖。Nurr1和NGFI-B的过表达可增强这种效应,而显性负性Nurr1变体则可消除这种效应。总之,FGF-8b诱导NR4A孤儿核受体的表达,这些受体参与介导FGF-8b在成骨细胞中的促生长作用。