Rydziel Sheila, Stadmeyer Lisa, Zanotti Stefano, Durant Deena, Smerdel-Ramoya Anna, Canalis Ernesto
Department of Research, Saint Francis Hospital and Medical Center, Hartford, Connecticut 06105, USA.
J Biol Chem. 2007 Jul 6;282(27):19762-72. doi: 10.1074/jbc.M700212200. Epub 2007 May 10.
Nephroblastoma overexpressed (Nov), a member of the Cyr 61, connective tissue growth factor, Nov (CCN) family of proteins, is expressed by osteoblasts, but its function in cells of the osteoblastic lineage is not known. We investigated the effects of Nov overexpression by transducing murine ST-2 stromal and MC3T3 osteoblastic cells with a retroviral vector where Nov is under the control of the cytomegalovirus promoter. We also examined the skeletal phenotype of transgenic mice expressing Nov under the control of the human osteocalcin promoter. Overexpression of Nov in ST-2 cells inhibited the appearance of mineralized nodules and decreased alkaline phosphatase activity and osteocalcin mRNA levels. Nov overexpression inhibited the effect of bone morphogenetic protein (BMP)-2 on the phosphorylation of Smad 1/5/8; on the transactivation of 12xSBE-Oc-pGL3, a BMP/Smad signaling reporter construct, and of Wnt 3 on cytoplasmic beta-catenin levels; and on the transactivation of the Wnt/beta-catenin signaling reporter construct 16xTCF-Luc. Nov overexpression did not activate Notch or transforming growth factor beta signaling. Glutathione S-transferase pulldown assays demonstrated direct Nov-BMP interactions. Nov transgenic mice exhibited osteopenia. In conclusion, Nov binds BMP-2 and antagonizes BMP-2 and Wnt activity, and its overexpression inhibits osteoblastogenesis and causes osteopenia.
肾母细胞瘤过度表达蛋白(Nov)是Cyr 61、结缔组织生长因子、Nov(CCN)蛋白家族的成员之一,由成骨细胞表达,但其在成骨细胞系细胞中的功能尚不清楚。我们通过用逆转录病毒载体转导小鼠ST-2基质细胞和MC3T3成骨细胞来研究Nov过表达的影响,该逆转录病毒载体中Nov受巨细胞病毒启动子控制。我们还检查了在人骨钙素启动子控制下表达Nov的转基因小鼠的骨骼表型。Nov在ST-2细胞中的过表达抑制了矿化结节的出现,降低了碱性磷酸酶活性和骨钙素mRNA水平。Nov过表达抑制了骨形态发生蛋白(BMP)-2对Smad 1/5/8磷酸化的作用;对BMP/Smad信号报告构建体12xSBE-Oc-pGL3以及Wnt 3对细胞质β-连环蛋白水平的反式激活作用;以及对Wnt/β-连环蛋白信号报告构建体16xTCF-Luc的反式激活作用。Nov过表达未激活Notch或转化生长因子β信号。谷胱甘肽S-转移酶下拉实验证明了Nov与BMP之间的直接相互作用。Nov转基因小鼠表现出骨质减少。总之,Nov与BMP-2结合并拮抗BMP-2和Wnt活性,其过表达抑制成骨细胞生成并导致骨质减少。