Mechanisms of Renal Calcium Transport
- 15 September 2000
- journal article
- review article
- Published by S. Karger AG in Nephron Experimental Nephrology
- Vol. 8 (6) , 343-350
- https://doi.org/10.1159/000020688
Abstract
The kidneys play a key role in the integrated regulation of calcium homeostasis. Calcium absorption takes place throughout the nephron. Proximal tubules, thick ascending limbs of Henle’s loop, and distal tubules are the major sites of calcium absorption. The mechanisms of absorption vary significantly from one segment to another, as does the extent of hormonal regulation. At one extreme is the considerable reabsorption by proximal tubules that proceeds primarily, if not entirely, by a paracellular pathway that is not regulated by hormones or drugs. In thick ascending limbs, calcium absorption occurs through a combination of transcellular and paracellular routes. The active, transcellular component is regulated by parathyroid hormone (PTH) and calcitonin, whereas the passive, paracellular route is governed by the extent of concomitant sodium absorption. At the other extreme is the distal tubule, where calcium absorption is entirely transcellular and is regulated by PTH, 1,25(OH)2vitamin D3, calcitonin, and by calcium-sparing drugs such as thiazide-type diuretics. The present review focuses on recent insights into the mechanisms of transcellular calcium movement and highlights the discovery of an epithelial calcium channel, ECaC, that may mediate calcium entry in distal tubules.Keywords
This publication has 13 references indexed in Scilit:
- Molecular Cloning and Characterization of a Channel-like Transporter Mediating Intestinal Calcium AbsorptionJournal of Biological Chemistry, 1999
- Cloning of a Stretch-inhibitable Nonselective Cation ChannelPublished by Elsevier ,1999
- Molecular Identification of the Apical Ca2+Channel in 1,25-Dihydroxyvitamin D3-responsive EpitheliaJournal of Biological Chemistry, 1999
- CODEPENDENCE OF RENAL CALCIUM AND SODIUM TRANSPORTAnnual Review of Physiology, 1998
- Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type IIINature Genetics, 1997
- Genetic heterogeneity of Barter's syndrome revealed by mutations in the K+ channel, ROMKNature Genetics, 1996
- Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporterNature Genetics, 1996
- Neural basis of saccade target selection in frontal eye field during visual searchNature, 1993
- Cloning and expression of an inwardly rectifying ATP-regulated potassium channelNature, 1993
- Activation of latent Ca2+ channels in renal epithelial cells by parathyroid hormoneNature, 1990