Hermey D C, Popoff S N, Marks S C
Department of Cell Biology, University of Massachusetts Medical Center, Worcester 01655, USA.
Connect Tissue Res. 1996;35(1-4):273-8. doi: 10.3109/03008209609029201.
Osteopetrosis is a heterogeneous group of metabolic bone disorders characterized by reduced bone resorption. In the toothless (tl) osteopetrotic rat mutation there are few osteoclasts and mutants are not cured by bone marrow transplants. This suggests that the defect(s) in tl rats is within the skeletal microenvironment and not one of stem cell incompetence. Osteoblasts are known to play a role in bone resorption and abnormalities in these cells have been reported in tl rats. We explored the ability of osteoblasts from tl rats to activate resorption by normal osteoclasts when co-cultured in the presence of 1,25-dihydroxyvitamin D (1,25(OH)2D). Stimulation with 1,25(OH)2D produced a highly significant response in normal osteoblast co-cultures, but no response was observed in mutant cultures over a wide dose range. Ligand-binding studies demonstrated no abnormalities in vitamin D receptor (VDR) affinity, but mutant osteoblasts had reduced VDR numbers. Taken together with the demonstrated resistance of these mutants to the hypercalcemic effects of 1,25(OH)2D and parathyroid hormone in vivo, these data implicate osteoblasts in the pathogenesis of this mutation.
骨质石化症是一组异质性的代谢性骨病,其特征是骨吸收减少。在无牙(tl)骨质石化大鼠突变体中,破骨细胞数量很少,且骨髓移植无法治愈突变体。这表明tl大鼠的缺陷在于骨骼微环境,而非干细胞功能不全。已知成骨细胞在骨吸收中起作用,并且在tl大鼠中已报道这些细胞存在异常。我们研究了在1,25 - 二羟基维生素D(1,25(OH)2D)存在下共培养时,tl大鼠成骨细胞激活正常破骨细胞进行吸收的能力。用1,25(OH)2D刺激在正常成骨细胞共培养物中产生了高度显著的反应,但在宽剂量范围内突变体培养物中未观察到反应。配体结合研究表明维生素D受体(VDR)亲和力无异常,但突变体成骨细胞的VDR数量减少。结合这些突变体在体内对1,25(OH)2D和甲状旁腺激素的高钙血症作用表现出抗性,这些数据表明成骨细胞参与了该突变的发病机制。