Koh Amy J, Demiralp Burak, Neiva Kathleen G, Hooten Joanna, Nohutcu Rahime M, Shim Hyunsuk, Datta Nabanita S, Taichman Russell S, McCauley Laurie K
Department of Periodontics and Oral Medicine, School of Dentistry, Room 3343, University of Michigan, 1011 North University Avenue, Ann Arbor, Michigan 48109-1078, USA.
Endocrinology. 2005 Nov;146(11):4584-96. doi: 10.1210/en.2005-0333. Epub 2005 Aug 4.
PTH is an anabolic agent used to treat osteoporosis, but its mechanisms of action are unclear. This study elucidated target cells and mechanisms for anabolic actions of PTH in mice during bone growth. Mice with c-fos ablation are osteopetrotic and lack an anabolic response to PTH. In this study, there were no alterations in PTH-regulated osteoblast differentiation or proliferation in vitro in cells from c-fos -/- mice compared with +/+; hence, the impact of osteoclastic cells was further investigated. A novel transplant model was used to rescue the osteopetrotic defect of c-fos ablation. Vertebral bodies (vossicles) from c-fos -/- and +/+ mice were implanted into athymic hosts, and the c-fos -/- osteoclast defect was rescued. PTH treatment to vossicle-bearing mice increased 5-bromo-2'-deoxyuridine (BrdU) positivity in the bone marrow and increased bone area regardless of the vossicle genotype. To inhibit recruitment of osteoclast precursors to wild-type vossicles, stromal derived factor-1 signaling was blocked, which blunted the PTH anabolic response. Treating mice with osteoprotegerin to inhibit osteoclast differentiation also blocked the anabolic action of PTH. In contrast, using c-src mutant mice with a late osteoclast differentiation defect did not hinder the anabolic action, suggesting key target cells reside in the intermediately differentiated osteoclast population in the bone marrow. These results indicate that c-fos in osteoblasts is not critical for PTH action but that cells of the osteoclast lineage are intermediate targets for the anabolic action of PTH.
甲状旁腺激素(PTH)是一种用于治疗骨质疏松症的促合成代谢药物,但其作用机制尚不清楚。本研究阐明了PTH在小鼠骨骼生长过程中促合成代谢作用的靶细胞和机制。c-fos基因敲除的小鼠患有骨质石化症,对PTH缺乏促合成代谢反应。在本研究中,与野生型小鼠相比,c-fos基因敲除小鼠的细胞在体外PTH调节的成骨细胞分化或增殖方面没有改变;因此,进一步研究了破骨细胞的影响。一种新型移植模型被用于挽救c-fos基因敲除导致的骨质石化缺陷。将c-fos基因敲除小鼠和野生型小鼠的椎体(小骨块)植入无胸腺宿主中,c-fos基因敲除小鼠的破骨细胞缺陷得到了挽救。对携带小骨块的小鼠进行PTH治疗,无论小骨块的基因型如何,均可增加骨髓中5-溴-2'-脱氧尿苷(BrdU)的阳性率并增加骨面积。为了抑制破骨细胞前体向野生型小骨块的募集,阻断了基质衍生因子-1信号传导,这减弱了PTH的促合成代谢反应。用骨保护素治疗小鼠以抑制破骨细胞分化也阻断了PTH的促合成代谢作用。相比之下,使用具有晚期破骨细胞分化缺陷的c-src突变小鼠并没有阻碍促合成代谢作用,这表明关键靶细胞存在于骨髓中中等分化的破骨细胞群体中。这些结果表明,成骨细胞中的c-fos对PTH作用并不关键,但破骨细胞谱系的细胞是PTH促合成代谢作用的中间靶标。