Claudins in barrier and transport function-the kidney

Pflugers Arch. 2017 Jan;469(1):105-113. doi: 10.1007/s00424-016-1906-6. Epub 2016 Nov 23.


Claudins are discovered to be key players in renal epithelial physiology. They are involved in developmental, physiological, and pathophysiological differentiation. In the glomerular podocytes, claudin-1 is an important determinant of cell junction fate. In the proximal tubule, claudin-2 plays important roles in paracellular salt reabsorption. In the thick ascending limb, claudin-14, -16, and -19 regulate the paracellular reabsorption of calcium and magnesium. Recessive mutations in claudin-16 or -19 cause an inherited calcium and magnesium losing disease. Synonymous variants in claudin-14 have been associated with hypercalciuric nephrolithiasis by genome-wide association studies (GWASs). More importantly, claudin-14 gene expression can be regulated by extracellular calcium levels via the calcium sensing receptor. In the distal tubules, claudin-4 and -8 form paracellular chloride pathway to facilitate electrogenic sodium reabsorption. Aldosterone, WNK4, Cap1, and KLHL3 are powerful regulators of claudin and the paracellular chloride permeability. The lessons learned on claudins from the kidney will have a broader impact on tight junction biology in other epithelia and endothelia.

Keywords: Calcium; Claudin; Epithelium; Glomerulus; Hypertension; Ion channel; Kidney; Kidney stone; Magnesium; Polarity; Tight junction.

Publication types

  • Review
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Claudins / genetics
  • Claudins / metabolism*
  • Gene Expression / genetics
  • Humans
  • Kidney Tubules, Proximal / metabolism*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Tight Junctions / metabolism


  • Claudins
  • Membrane Proteins