Rowe Peter S N, Matsumoto Naoko, Jo Oak D, Shih Remi N J, Oconnor Jeannine, Roudier Martine P, Bain Steve, Liu Shiguang, Harrison Jody, Yanagawa Norimoto
Department of Internal Medicine, The Kidney Institute and Division of Nephrology, MS 3018, University of Kansas Medical Center, 3901 Rainbow Boulevard, 6020B Wahl Hall East, Kansas City, KS 66160, USA.
Bone. 2006 Oct;39(4):773-86. doi: 10.1016/j.bone.2006.04.012. Epub 2006 Jun 9.
Increased expression of several osteoblastic proteases and MEPE (a bone matrix protein) occurs in X-linked hypophosphatemic rickets (hyp). This is associated with an increased release of a protease-resistant MEPE peptide (ASARM peptide), a potent inhibitor of mineralization. Cathepsin B cleaves MEPE releasing ASARM peptide and hyp osteoblast/osteocyte cells hypersecrete cathepsin D, an activator of cathepsin B. Our aims were to determine whether cathepsin inhibitors correct the mineralization defect in vivo and whether hyp-bone ASARM peptide levels are reduced after protease treatment. Normal littermates and hyp mice (n = 6) were injected intraperitoneally once a day for 4 weeks with pepstatin, CAO74 or vehicle. Animals were then sacrificed and bones plus serum removed for comprehensive analysis. All hyp mice groups (treated and untreated) remained hypophosphatemic with serum 1,25 vitamin D3 inappropriately normal. Serum PTH was significantly elevated in all hyp mice groups relative to normal mice (P = 0.0017). Untreated hyp mice had six-fold elevated levels of serum alkaline-phosphatase and two-fold elevated levels of ASARM peptides relative to normal mice (P < 0.001). In contrast, serum alkaline phosphatase and serum ASARM peptides were significantly reduced (normalized) in hyp mice treated with CA074 or pepstatin. Serum FGF23 levels remained high in all hyp animal groups (P < 0.0001). Hyp mice treated with protease inhibitors showed dramatic reductions in unmineralized osteoid (femurs) compared to control hyp mice (Goldner staining). Also, hyp animals treated with protease inhibitors showed marked and significant improvements in growth plate width (42%), osteoid thickness (40%) and cortical area (40%) (P < 0.002). The mineralization apposition rate, bone formation rate and mineralization surface were normalized by protease-treatment. High-resolution pQCT mineral histomorphometry measurements and uCT also confirmed a marked mineralization improvement. Finally, the growth plate and cortical bone of hyp femurs contained a massive accumulation of osteoblast-derived ASARM peptide(s) that was reduced in hyp animals treated with CA074 or pepstatin. This study confirms in vivo administration of cathepsin inhibitors improves bone mineralization in hyp mice. This may be due to a protease inhibitor mediated decrease in proteolytic degradation of the extracellular matrix and a reduced release of ASARM peptides (potent mineralization inhibitors).
几种成骨蛋白酶和MEPE(一种骨基质蛋白)的表达增加出现在X连锁低磷性佝偻病(hyp)中。这与一种抗蛋白酶的MEPE肽(ASARM肽)释放增加有关,ASARM肽是一种有效的矿化抑制剂。组织蛋白酶B切割MEPE释放出ASARM肽,并且hyp成骨细胞/骨细胞过度分泌组织蛋白酶D,而组织蛋白酶D是组织蛋白酶B的激活剂。我们的目的是确定组织蛋白酶抑制剂是否能在体内纠正矿化缺陷,以及蛋白酶治疗后hyp骨中ASARM肽水平是否降低。正常同窝幼崽和hyp小鼠(n = 6)每天腹腔注射一次胃蛋白酶抑制剂、CAO74或赋形剂,持续4周。然后处死动物,取出骨骼和血清进行全面分析。所有hyp小鼠组(治疗组和未治疗组)仍为低磷血症,血清1,25-维生素D3水平异常正常。与正常小鼠相比,所有hyp小鼠组的血清甲状旁腺激素显著升高(P = 0.0017)。与正常小鼠相比,未治疗的hyp小鼠血清碱性磷酸酶水平升高6倍,ASARM肽水平升高2倍(P < 0.001)。相比之下,用CA074或胃蛋白酶抑制剂治疗的hyp小鼠血清碱性磷酸酶和血清ASARM肽显著降低(恢复正常)。所有hyp动物组的血清FGF23水平仍然很高(P < 0.0001)。与对照hyp小鼠相比,用蛋白酶抑制剂治疗的hyp小鼠未矿化类骨质(股骨)显著减少(戈德纳染色)。此外,用蛋白酶抑制剂治疗的hyp动物在生长板宽度(42%)、类骨质厚度(40%)和皮质面积(40%)方面显示出显著且明显的改善(P < 0.002)。通过蛋白酶治疗,矿化沉积率、骨形成率和矿化表面恢复正常。高分辨率pQCT矿化组织形态计量学测量和uCT也证实矿化有显著改善。最后,hyp股骨的生长板和皮质骨中含有大量成骨细胞衍生的ASARM肽积累,在用CA074或胃蛋白酶抑制剂治疗的hyp动物中这种积累减少。这项研究证实,在体内给予组织蛋白酶抑制剂可改善hyp小鼠的骨矿化。这可能是由于蛋白酶抑制剂介导的细胞外基质蛋白水解降解减少以及ASARM肽(有效的矿化抑制剂)释放减少所致。