The Cap1–claudin-4 regulatory pathway is important for renal chloride reabsorption and blood pressure regulation

Y Gong, M Yu, J Yang, E Gonzales… - Proceedings of the …, 2014 - National Acad Sciences
Y Gong, M Yu, J Yang, E Gonzales, R Perez, M Hou, P Tripathi, KS Hering-Smith, LL Hamm
Proceedings of the National Academy of Sciences, 2014National Acad Sciences
The paracellular pathway through the tight junction provides an important route for
transepithelial chloride reabsorption in the kidney, which regulates extracellular salt content
and blood pressure. Defects in paracellular chloride reabsorption may in theory cause
deregulation of blood pressure. However, there is no evidence to prove this theory or to
demonstrate the in vivo role of the paracellular pathway in renal chloride handling. Here,
using a tissue-specific KO approach, we have revealed a chloride transport pathway in the …
The paracellular pathway through the tight junction provides an important route for transepithelial chloride reabsorption in the kidney, which regulates extracellular salt content and blood pressure. Defects in paracellular chloride reabsorption may in theory cause deregulation of blood pressure. However, there is no evidence to prove this theory or to demonstrate the in vivo role of the paracellular pathway in renal chloride handling. Here, using a tissue-specific KO approach, we have revealed a chloride transport pathway in the kidney that requires the tight junction molecule claudin-4. The collecting duct-specific claudin-4 KO animals developed hypotension, hypochloremia, and metabolic alkalosis due to profound renal wasting of chloride. The claudin-4–mediated chloride conductance can be regulated endogenously by a protease—channel-activating protease 1 (cap1). Mechanistically, cap1 regulates claudin-4 intercellular interaction and membrane stability. A putative cap1 cleavage site has been identified in the second extracellular loop of claudin-4, mutation of which abolished its regulation by cap1. The cap1 effects on paracellular chloride permeation can be extended to other proteases such as trypsin, suggesting a general mechanism may also exist for proteases to regulate the tight junction permeabilities. Together, we have discovered a theory that paracellular chloride permeability is physiologically regulated and essential to renal salt homeostasis and blood pressure control.
National Acad Sciences