J Bone Miner Res. 2014 Jun;29(6):1424-30. doi: 10.1002/jbmr.2152.
Bone formation can be remodeling-based (RBF) or modeling-based (MBF), the former coupled to bone resorption and the latter occurring directly on quiescent surfaces. Unlike osteoanabolic therapies such as parathyroid hormone (PTH) 1-34 that increase bone remodeling and thus both formation and resorption, sclerostin antibody (Scl-Ab) increases bone formation while decreasing bone resorption. With this unique profile, we tested our hypothesis that Scl-Ab primarily elicited MBF by examining bones from Scl-Ab–treated ovariectomized (OVX) rats and male cynomolgus monkeys (cynos). Histomorphometry was performed to quantify and characterize bone surfaces in OVX rats administered vehicle or Scl-Ab (25 mg/kg) subcutaneously (sc) twice/week for 5 weeks and in adolescent cynos administered vehicle or Scl-Ab (30 mg/kg) sc every 2 weeks for 10 weeks. Fluorochrome-labeled surfaces in L2 vertebra and femur endocortex (cynos only) were considered to be MBF or RBF based on characteristics of their associated cement lines. In OVX rats, Scl-Ab increased MBF by eightfold (from 7% to 63% of bone surface, compared to vehicle). In cynos, Scl-Ab markedly increased MBF on trabecular (from 0.6% to 34%) and endocortical surfaces (from 7% to 77%) relative to vehicle. Scl-Ab did not significantly affect RBF in rats or cynos despite decreased resorption surface in both species. In cynos, Scl-Ab resulted in a greater proportion of RBF and MBF containing sequential labels from week 2, indicating an increase in the lifespan of the formative site. This extended formation period was associated with robust increases in the percent of new bone volume formed. These results demonstrate that Scl-Ab increased bone volume by increasing MBF and prolonged the formation period at both modeling and remodeling sites while reducing bone resorption. Through these unique effects on bone formation and resorption, Scl-Ab may prove to be an effective therapeutic to rapidly increase bone mass in diseases such as osteoporosis.
骨形成可以是基于重塑的(RBF)或基于建模的(MBF),前者与骨吸收偶联,后者直接发生在静止表面上。与甲状旁腺激素(PTH)1-34 等增加骨重塑从而增加形成和吸收的骨合成代谢疗法不同,硬骨素抗体(Scl-Ab)增加骨形成的同时减少骨吸收。基于这种独特的特征,我们通过检查 Scl-Ab 治疗的去卵巢(OVX)大鼠和雄性食蟹猴(cynos)的骨骼,来检验我们的假设,即 Scl-Ab 主要通过 MBF 发挥作用。对接受载体或 Scl-Ab(25mg/kg)皮下(sc)每周两次共 5 周治疗的 OVX 大鼠和每两周接受载体或 Scl-Ab(30mg/kg)sc 共 10 周的青少年 cynos 进行组织形态计量学分析,以定量和描述骨表面。L2 椎骨和股骨内皮层(仅 cynos)的荧光标记表面根据其相关的粘合线的特征被认为是 MBF 或 RBF。在 OVX 大鼠中,Scl-Ab 将 MBF 增加了八倍(从 7%增加到 63%的骨表面,与载体相比)。在 cynos 中,与载体相比,Scl-Ab 使小梁(从 0.6%增加到 34%)和内皮层表面(从 7%增加到 77%)的 MBF 明显增加。尽管两种动物的吸收表面均减少,但 Scl-Ab 对大鼠或 cynos 的 RBF 没有显著影响。在 cynos 中,从第 2 周开始,Scl-Ab 导致具有连续标记的 RBF 和 MBF 的比例更大,表明形成部位的寿命延长。这一延长的形成期与新骨体积形成百分比的大幅增加有关。这些结果表明,Scl-Ab 通过增加 MBF 增加了骨量,并在重塑和建模部位延长了形成期,同时减少了骨吸收。通过对骨形成和吸收的这些独特影响,Scl-Ab 可能成为一种有效的治疗方法,可快速增加骨质疏松症等疾病的骨量。