Molecular genetic study of congenital nephrogenic diabetes insipidus and rescue of mutant vasopressin V2 receptor by chemical chaperones

Nephrology (Carlton). 2007 Apr;12(2):113-7. doi: 10.1111/j.1440-1797.2006.00759.x.

Abstract

Aim: X-linked nephrogenic diabetes insipidus is a rare disease caused by mutations in the arginine vasopressin V2 receptor (AVPR2) gene, which encodes vasopressin V2 receptor (V2R). More than a half of reported mutations in AVPR2 are missense mutations, and a large number of missense mutant receptors fail to fold properly and therefore are not routed to the cell surface.

Methods: We analysed the AVPR2 gene in 14 unrelated patients with X-linked nephrogenic diabetes insipidus, and found 13 different mutations including eight missense point mutations. The cellular expression patterns of three missense mutant (A98P, L274P and R113W) and wild-type V2R were determined in transfected COS-7 cells.

Results: In contrast to wild-type V2R, the cell-surface expressions of mutant receptors were totally (A98P and L274P) or partially (R113W) absent. Instead, they were retained intracellularly. However, treatment of cells with two chemical chaperones (100 mmol/L trimethylamine oxide or 2% dimethyl sulfoxide) or incubation at 26 degrees C restored the cell-surface expressions of mutant receptors.

Conclusion: These data show that some chemical chaperones correct the mistrafficking of misfolded A98P, L274P and R113W V2R. Thus, we believe that a therapeutic strategy based on chemical chaperones in patients with these mutations is worth trying.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginine Vasopressin / genetics
  • Arginine Vasopressin / metabolism*
  • COS Cells
  • Cell Membrane / metabolism
  • Chlorocebus aethiops
  • Diabetes Insipidus, Nephrogenic / genetics
  • Diabetes Insipidus, Nephrogenic / metabolism*
  • Dimethyl Sulfoxide / pharmacology*
  • Humans
  • Male
  • Methylamines / pharmacology*
  • Molecular Chaperones / pharmacology
  • Mutation*
  • Mutation, Missense
  • Point Mutation
  • Protein Folding
  • Protein Transport / drug effects
  • Receptors, Vasopressin / chemistry
  • Receptors, Vasopressin / genetics
  • Receptors, Vasopressin / metabolism*
  • Temperature
  • Transfection

Substances

  • Methylamines
  • Molecular Chaperones
  • Receptors, Vasopressin
  • Arginine Vasopressin
  • trimethylamine
  • Dimethyl Sulfoxide