Hernando Nati, Gisler Serge M, Reining Sonja C, Déliot Nadine, Capuano Paola, Biber Jürg, Murer Heini
Institute of Physiology and Zurich Center for Integrative Human Physiology (ZIHP), University of Zurich, Winterthurerstr. 190, 8057 Zurich, Switzerland.
Urol Res. 2010 Aug;38(4):271-6. doi: 10.1007/s00240-010-0304-3. Epub 2010 Jul 28.
Control of phosphate (P(i)) homeostasis is essential for many biologic functions and inappropriate low levels of P(i) in plasma have been suggested to associate with several pathological states, including renal stone formation and stone recurrence. P(i) homeostasis is achieved mainly by adjusting the renal reabsorption of P(i) to the body's requirements. This task is performed to a major extent by the Na/Pi cotransporter NaPi-IIa that is specifically expressed in the brush border membrane of renal proximal tubules. While the presence of tight junctions in epithelial cells prevents the diffusion and mixing of the apical and basolateral components, the location of a protein within a particular membrane subdomain (i.e., the presence of NaPi-IIa at the tip of the apical microvilli) often requires its association with scaffolding elements which directly or indirectly connect the protein with the underlying cellular cytoskeleton. NaPi-IIa interacts with the four members of the Na(+)/H(+) exchanger regulatory factor family as well as with the GABA(A)-receptor associated protein . Here we will discuss the most relevant findings regarding the role of these proteins on the expression and regulation of the cotransporter, as well as the impact that their absence has in P(i) homeostasis.
控制磷酸盐(P(i))稳态对于许多生物学功能至关重要,血浆中P(i)水平异常降低被认为与多种病理状态相关,包括肾结石形成和结石复发。P(i)稳态主要通过根据身体需求调节肾脏对P(i)的重吸收来实现。这项任务在很大程度上由钠/磷共转运蛋白NaPi-IIa完成,该蛋白在肾近端小管刷状缘膜中特异性表达。虽然上皮细胞中的紧密连接可防止顶端和基底外侧成分的扩散和混合,但蛋白质在特定膜亚结构域中的定位(即NaPi-IIa存在于顶端微绒毛尖端)通常需要其与支架元件结合,这些支架元件直接或间接将蛋白质与潜在的细胞细胞骨架相连。NaPi-IIa与钠/氢交换调节因子家族的四个成员以及γ-氨基丁酸A(GABA(A))受体相关蛋白相互作用。在此,我们将讨论这些蛋白质在共转运蛋白表达和调节方面的最相关发现,以及它们缺失对P(i)稳态的影响。