Ono Noriaki, Nakashima Kazuhisa, Schipani Ernestina, Hayata Tadayoshi, Ezura Yoichi, Soma Kunimichi, Kronenberg Henry M, Noda Masaki
Department of Molecular Pharmacology, Medical Research Institute, Graduate School, Tokyo Medical and Dental University, and Endocrine Unit, Massachusetts General Hospital, Boston 02114, USA.
J Biol Chem. 2007 Aug 31;282(35):25509-16. doi: 10.1074/jbc.M610782200. Epub 2007 May 11.
Multiple signaling pathways participate in the regulation of bone remodeling, and pathological negative balance in the regulation results in osteoporosis. However, interactions of signaling pathways that act comprehensively in concert to maintain bone mass are not fully understood. We investigated roles of parathyroid hormone receptor (PTH/PTHrP receptor) signaling in osteoblasts in unloading-induced bone loss using transgenic mice. Hind limb unloading by tail suspension reduced bone mass in wild-type mice. In contrast, signaling by constitutively active PTH/PTHrP receptor (caPPR), whose expression was regulated by the osteoblast-specific Col1a1 promoter (Col1a1-caPPR), suppressed unloading-induced reduction in bone mass in these transgenic mice. In Col1a1-caPPR transgenic (Tg) mice, hind limb unloading suppressed bone formation parameters in vivo and mineralized nodule formation in vitro similarly to those observed in wild-type mice. In addition, serum osteocalcin levels and mRNA expression levels of type I collagen, Runx2 and Osterix in bone were suppressed by unloading in both wild-type mice and Tg mice. However, in contrast to unloading-induced enhancement of bone resorption parameters in wild-type mice, Col1a1-caPPR signaling suppressed, rather than enhanced, osteoclast number and osteoclast surface as well as urinary deoxypyridinoline excretion upon unloading. Col1a1-caPPR signaling also suppressed mRNA expression levels of RANK and c-fms in bone upon unloading. Although the M-CSF and monocyte chemoattractant protein 1 (MCP-1) mRNA levels were enhanced in control Tg mice, these levels were suppressed in unloaded Tg mice. These results indicated that constitutive activation of PTH/PTHrP receptor signaling in osteoblastic cells suppresses unloading-induced bone loss specifically through the regulation of osteoclastic activity.
多种信号通路参与骨重塑的调节,调节过程中的病理性负平衡会导致骨质疏松症。然而,共同作用以维持骨量的信号通路之间的相互作用尚未完全明确。我们利用转基因小鼠研究了甲状旁腺激素受体(PTH/PTHrP受体)信号通路在成骨细胞中对卸载诱导的骨质流失的作用。通过尾部悬吊进行后肢卸载可降低野生型小鼠的骨量。相比之下,由成骨细胞特异性Col1a1启动子(Col1a1-caPPR)调控表达的组成型活性PTH/PTHrP受体(caPPR)发出的信号,可抑制这些转基因小鼠中卸载诱导的骨量减少。在Col1a1-caPPR转基因(Tg)小鼠中,后肢卸载在体内抑制骨形成参数,在体外抑制矿化结节形成,这与在野生型小鼠中观察到的情况相似。此外,野生型小鼠和Tg小鼠在卸载后,血清骨钙素水平以及骨中I型胶原蛋白、Runx2和Osterix的mRNA表达水平均受到抑制。然而,与卸载诱导野生型小鼠骨吸收参数增强相反,Col1a1-caPPR信号通路在卸载时抑制而不是增强破骨细胞数量、破骨细胞表面积以及尿脱氧吡啶啉排泄。Col1a1-caPPR信号通路在卸载时还抑制骨中RANK和c-fms的mRNA表达水平。虽然在对照Tg小鼠中M-CSF和单核细胞趋化蛋白1(MCP-1)的mRNA水平升高,但在卸载的Tg小鼠中这些水平受到抑制。这些结果表明,成骨细胞中PTH/PTHrP受体信号通路的组成型激活通过特异性调节破骨细胞活性来抑制卸载诱导的骨质流失。