Abstract

Inorganic phosphate (Pi) homeostasis is maintained by the tight regulation of renal Pi excretion versus reabsorption rates that are in turn modulated by adjusting the number of Pi transporters (mainly NaPi-2a) in the proximal tubules. In response to some hormones and a high dietary Pi content, NaPi-2a is endocytosed and degraded in the lysosomes; however, we show here that some NaPi-2a molecules are targeted to the trans-Golgi network (TGN) during the endocytosis. In the TGN, NaPi-2a interacts with PIST (PDZ-domain protein interacting specifically with TC10), a TGN-resident PDZ-domain-containing protein. The extension of the interaction is proportional to the expression of NaPi-2a in the TGN, and, consistent with that, it is increased with a high Pi diet. When overexpressed in opossum kidney (OK) cells, PIST retains NaPi-2a in the TGN and inhibits Na-dependent Pi transport. Overexpression of PIST also prevents the adaptation of OK cells to a low Pi culture medium. Our data supports the view that NaPi-2a is subjected to retrograde trafficking from the plasma membrane to the TGN using one of the machineries involved in endosomal transport and explains the reported expression of NaPi-2a in the TGN.

Highlights

  • The proximal tubule of the kidney is the main anatomical structure that maintains inorganic phosphate (Pi) homeostasis, by virtue of its ability to fine-tune the Pi reabsorption rate

  • Renal Pi excretion and reabsorption depend on the abundance of specific Na-dependent Pi transporters expressed in the brush-border membrane of the proximal tubular epithelial cells [1]

  • In addition to the main expression of NaPi-2a in the brush-border membrane of proximal tubular cells, this Pi transporter exhibits a perinuclear staining, which is compatible with a specific expression in the trans-Golgi network [7, 13]

Read more

Summary

Introduction

The proximal tubule of the kidney is the main anatomical structure that maintains inorganic phosphate (Pi) homeostasis, by virtue of its ability to fine-tune the Pi reabsorption rate. Renal Pi excretion and reabsorption depend on the abundance of specific Na-dependent Pi transporters expressed in the brush-border membrane of the proximal tubular epithelial cells [1]. This abundance is controlled by several hormonal and nonhormonal agents, including phosphatonins, parathyroid hormone (PTH), and dietary Pi concentration [2]. Two type II Pi transporters (NaPi-2a and NaPi-2c) and two type III transporters (PiT-1 and PiT-2) are expressed in the proximal tubule of the nephron. NaPi-2a has been the most characterized Pi transporter, and the cellular mechanisms that regulate the apical expression of NaPi-2a in response to PTH or dietary Pi concentration have been extensively studied

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call