Department of Medicine, University of Wisconsin-Madison and Geriatric Research and Education Center, William S. Middleton Memorial Veterans Hospital, Madison, WI, USA.
J Bone Miner Res. 2013 Jan;28(1):56-72. doi: 10.1002/jbmr.1738.
Inactivating mutations of the "phosphate regulating gene with homologies to endopeptidases on the X chromosome" (PHEX/Phex) underlie disease in patients with X-linked hypophosphatemia (XLH) and the hyp-mouse, a murine homologue of the human disorder. Although increased serum fibroblast growth factor 23 (FGF-23) underlies the HYP phenotype, the mechanism(s) by which PHEX mutations inhibit FGF-23 degradation and/or enhance production remains unknown. Here we show that treatment of wild-type mice with the proprotein convertase (PC) inhibitor, decanoyl-Arg-Val-Lys-Arg-chloromethyl ketone (Dec), increases serum FGF-23 and produces the HYP phenotype. Because PC2 is uniquely colocalized with PHEX in osteoblasts/bone, we examined if PC2 regulates PHEX-dependent FGF-23 cleavage and production. Transfection of murine osteoblasts with PC2 and its chaperone protein 7B2 cleaved FGF-23, whereas Signe1 (7B2) RNA interference (RNAi) transfection, which limited 7B2 protein production, decreased FGF-23 degradation and increased Fgf-23 mRNA and protein. The mechanism by which decreased 7B2•PC2 activity influences Fgf-23 mRNA was linked to reduced conversion of the precursor to bone morphogenetic protein 1 (proBMP1) to active BMP1, which resulted in limited cleavage of dentin matrix acidic phosphoprotein 1 (DMP1), and consequent increased Fgf-23 mRNA. The significance of decreased 7B2•PC2 activity in XLH was confirmed by studies of hyp-mouse bone, which revealed significantly decreased Sgne1 (7B2) mRNA and 7B2 protein, and limited cleavage of proPC2 to active PC2. The expected downstream effects of these changes included decreased FGF-23 cleavage and increased FGF-23 synthesis, secondary to decreased BMP1-mediated degradation of DMP1. Subsequent Hexa-D-Arginine treatment of hyp-mice enhanced bone 7B2•PC2 activity, normalized FGF-23 degradation and production, and rescued the HYP phenotype. These data suggest that decreased PHEX-dependent 7B2•PC2 activity is central to the pathogenesis of XLH.
“X 染色体同源内肽酶的磷酸调节基因”(PHEX/Phex)的失活突变是 X 连锁低磷血症(XLH)和低鼠(人类疾病的鼠类同源物)发病的基础。尽管血清成纤维细胞生长因子 23(FGF-23)的增加是 HYP 表型的基础,但 PHEX 突变抑制 FGF-23 降解和/或增强其产生的机制仍不清楚。在这里,我们表明,用前蛋白转化酶(PC)抑制剂 decanoyl-Arg-Val-Lys-Arg-chloromethyl ketone(Dec)处理野生型小鼠会增加血清 FGF-23 并产生 HYP 表型。因为 PC2 仅与成骨细胞/骨中的 PHEX 共定位,所以我们检查了 PC2 是否调节 PHEX 依赖性 FGF-23 切割和产生。用 PC2 和其伴侣蛋白 7B2 转染鼠成骨细胞可切割 FGF-23,而 Signe1(7B2)RNA 干扰(RNAi)转染,其限制 7B2 蛋白的产生,减少 FGF-23 降解并增加 Fgf-23mRNA 和蛋白。降低 7B2•PC2 活性影响 Fgf-23mRNA 的机制与骨形态发生蛋白 1(proBMP1)前体转化为活性 BMP1 的减少有关,这导致牙本质基质酸性磷酸蛋白 1(DMP1)的有限切割,继而增加 Fgf-23mRNA。用 hyp-mouse 骨进行的研究证实了降低的 7B2•PC2 活性在 XLH 中的意义,该研究显示 Sgne1(7B2)mRNA 和 7B2 蛋白显著降低,并且 proPC2 到活性 PC2 的有限切割。这些变化的预期下游影响包括由于 DMP1 介导的 FGF-23 降解减少,FGF-23 切割减少和合成增加。随后用 Hexa-D-Arginine 处理 hyp-mice 增强了骨 7B2•PC2 活性,使 FGF-23 降解和产生正常化,并挽救了 HYP 表型。这些数据表明,PHEX 依赖性 7B2•PC2 活性的降低是 XLH 发病机制的核心。