Miyamoto Ken-ichi, Segawa Hiroko, Ito Mikiko, Kuwahata Masashi
Nutritional Science, Department of Nutrition, School of Medicine, Tokushima University, Tokushima, 770-8503 Japan.
Jpn J Physiol. 2004 Apr;54(2):93-102. doi: 10.2170/jjphysiol.54.93.
The physiological regulation of renal Pi reabsorption is mediated by renal type II Na/Pi cotransporters (type IIa and type IIc). The type IIa transporter is regulated, among other factors, by dietary Pi intake and parathyroid hormone (PTH). The PTH-induced inhibition of Pi reabsorption is mediated by endocytosis of the type IIa transporter from the brush-border membrane and subsequent lysosomal degradation. Type IIa is part of the heteromeric protein complexes organized by PDZ proteins. Furthermore, during Pi depletion the type IIc Na/Pi cotransporter is induced in the apical membrane of proximal tubular cells. The type IIc transporter is also regulated by PTH via internalization, but by a vesicular transport pathway distinct from that used by the type IIc transporter. Studying the mechanisms of type IIa and type IIc transporters has increased the understanding of the control of proximal tubular Pi handling and thus of overall Pi homeostasis.
肾脏对磷重吸收的生理调节由肾II型钠/磷共转运体(IIa型和IIc型)介导。IIa型转运体受多种因素调节,包括饮食中磷的摄入量和甲状旁腺激素(PTH)。PTH诱导的磷重吸收抑制是通过IIa型转运体从刷状缘膜的内吞作用以及随后的溶酶体降解介导的。IIa型是由PDZ蛋白组织的异源蛋白复合物的一部分。此外,在磷缺乏期间,IIc型钠/磷共转运体在近端小管细胞的顶膜中被诱导。IIc型转运体也通过内化受PTH调节,但通过与IIa型转运体不同的囊泡运输途径。对IIa型和IIc型转运体机制的研究增进了对近端小管磷处理控制的理解,从而也增进了对整体磷稳态的理解。