Segawa Hiroko, Miyamoto Kenichi
Department of Molecular Nutrition, Institute of Health Biosciences, the University of Tokushima Graduate School.
Clin Calcium. 2004 Jun;14(6):49-54.
The physiological regulation of renal Pi reabsorption is mediated by renal type II Na/Pi cotransporters. The type II a transporter is a key player of renal Pi reabsorption and regulated, among other factors, by parathyroid hormone (PTH). The PTH-induced inhibition of Pi reabsorption is mediated by endocytosis of the type II a transporter from the brush-border membrane and subsequent lysosomal degradation. In addition, during weaning, the type II c Na/Pi cotransporter (growth related Na/Pi cotransporter) is induced in the apical membrane of proximal tubular cells. The type II c transporter is also regulated by PTH, FGF-23 and PHEX. Studying the mechanisms of the regulation of type II c transporters by PHEX and FGF-23 has increased understanding of the control of proximal tubular Pi handling and bone mineralization.
肾脏磷重吸收的生理调节由肾脏II型钠/磷共转运体介导。II a型转运体是肾脏磷重吸收的关键参与者,除其他因素外,它受甲状旁腺激素(PTH)调节。PTH诱导的磷重吸收抑制是由II a型转运体从刷状缘膜内吞并随后被溶酶体降解介导的。此外,在断奶期间,II c型钠/磷共转运体(生长相关钠/磷共转运体)在近端肾小管细胞的顶膜中被诱导。II c型转运体也受PTH、成纤维细胞生长因子-23(FGF-23)和磷酸调节内肽酶同源物(PHEX)调节。研究PHEX和FGF-23对II c型转运体的调节机制,增进了对近端肾小管磷处理和骨矿化控制的理解。