Abstract

The exact distributions of the different salt transport systems along the human cortical distal nephron are unknown. Immunohistochemistry was performed on serial cryostat sections of healthy parts of tumor nephrectomized human kidneys to study the distributions in the distal convolution of the thiazide-sensitive Na-Cl cotransporter (NCC), the beta subunit of the amiloride-sensitive epithelial Na channel (ENaC), the vasopressin-sensitive water channel aquaporin 2 (AQP2), and aquaporin 3 (AQP3), the H(+) ATPase, the Na-Ca exchanger (NCX), plasma membrane calcium-ATPase, and calbindin-D28k (CaBP). The entire human distal convolution and the cortical collecting duct (CCD) display calbindin-D28k, although in variable amounts. Approximately 30% of the distal convolution profiles reveal NCC, characterizing the distal convoluted tubule. NCC overlaps with ENaC in a short portion at the end of the distal convoluted tubule. ENaC is displayed all along the connecting tubule (70% of the distal convolution) and the CCD. The major part of the connecting tubule and the CCD coexpress aquaporin 2 with ENaC. Intercalated cells, undetected in the first 20% of the distal convolution, were interspersed among the segment-specific cells of the remainder of the distal convolution, and of the CCD. The basolateral calcium extruding proteins, Na-Ca exchanger (NCX), and the plasma membrane Ca(2+)-ATPase were found all along the distal convolution, and, in contrast to other species, along the CCD, although in varying amounts. The knowledge regarding the precise distribution patterns of transport proteins in the human distal nephron and the knowledge regarding the differences from that in laboratory animals may be helpful for diagnostic purposes and may also help refine the therapeutic management of electrolyte disorders.

Highlights

  • The cortical distal nephron is the site for fine regulation of salt and water excretion by peptide and mineralocorticoid hormones and the site for specific actions of diuretics [1]

  • The aim of the study presented here was to show by immunochemistry the distribution patterns along the human distal convolution of a set of apical salt and water transport proteins (NCC, epithelial Na channel (ENaC), aquaporin 2 (AQP2))

  • Our study provides a comprehensive analysis on the immunohistochemical localization along the human distal convolution of the major renal Naϩ and water transporting proteins, the Na-Cl cotransporter (NCC), ENaC, and AQP2, and of basolateral proteins involved in regulated, transcellular transport of Ca2ϩ ions

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Summary

Introduction

The cortical distal nephron is the site for fine regulation of salt and water excretion by peptide and mineralocorticoid hormones and the site for specific actions of diuretics [1]. In humans alterations of BP [2,3,4], as well as some disorders of sodium, potassium, calcium, magnesium, and volume homeostasis [3], have been associated with mutations of genes encoding for salt and water transport proteins in the distal nephron [5,6,7,8]. The aim of the study presented here was to show by immunochemistry the distribution patterns along the human distal convolution of a set of apical salt and water transport proteins (NCC, ENaC, AQP2). Our results demonstrate that as in other mammalian species, the apical transport proteins in the human distal nephron are serially arranged, but their detailed distribution patterns differ markedly from those in laboratory animals

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