1. Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage
- Author
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Klar, Joakim, Piontek, Jörg, Milatz, Susanne, Tariq, Muhammad, Jameel, Muhammad, Breiderhoff, Tilman, Schuster, Jens, Fatima, Ambrin, Asif, Maria, Sher, Muhammad, Mäbert, Katrin, Fromm, Anja, Baig, Shahid M., Günzel, Dorothee, and Dahl, Niklas
- Subjects
Cell Physiology ,lcsh:QH426-470 ,endocrine system diseases ,Cell Membranes ,Materials Science ,Material Properties ,Mutation, Missense ,Research and Analysis Methods ,Kidney ,digestive system ,Physical Chemistry ,Permeability ,Tight Junctions ,Mice ,Exocrine Glands ,Cations ,Medicine and Health Sciences ,Animals ,Humans ,Protein Isoforms ,Renal Insufficiency ,Medicinsk genetik ,Skin ,Ions ,Staining ,Hypohidrosis ,urogenital system ,Biology and Life Sciences ,Membrane Proteins ,Kidneys ,Biological Transport ,Epithelial Cells ,Renal System ,Cell Biology ,Sweat Glands ,Membrane Staining ,lcsh:Genetics ,Chemistry ,Microscopy, Electron ,Specimen Preparation and Treatment ,Physical Sciences ,Claudins ,Anatomy ,Cellular Structures and Organelles ,Integumentary System ,Junctional Complexes ,Medical Genetics ,tissues ,Research Article - Abstract
Claudins constitute the major component of tight junctions and regulate paracellular permeability of epithelia. Claudin-10 occurs in two major isoforms that form paracellular channels with ion selectivity. We report on two families segregating an autosomal recessive disorder characterized by generalized anhidrosis, severe heat intolerance and mild kidney failure. All affected individuals carry a rare homozygous missense mutation c.144C>G, p.(N48K) specific for the claudin-10b isoform. Immunostaining of sweat glands from patients suggested that the disease is associated with reduced levels of claudin-10b in the plasma membranes and in canaliculi of the secretory portion. Expression of claudin-10b N48K in a 3D cell model of sweat secretion indicated perturbed paracellular Na+ transport. Analysis of paracellular permeability revealed that claudin-10b N48K maintained cation over anion selectivity but with a reduced general ion conductance. Furthermore, freeze fracture electron microscopy showed that claudin-10b N48K was associated with impaired tight junction strand formation and altered cis-oligomer formation. These data suggest that claudin-10b N48K causes anhidrosis and our findings are consistent with a combined effect from perturbed TJ function and increased degradation of claudin-10b N48K in the sweat glands. Furthermore, affected individuals present with Mg2+ retention, secondary hyperparathyroidism and mild kidney failure that suggest a disturbed reabsorption of cations in the kidneys. These renal-derived features recapitulate several phenotypic aspects detected in mice with kidney specific loss of both claudin-10 isoforms. Our study adds to the spectrum of phenotypes caused by tight junction proteins and demonstrates a pivotal role for claudin-10b in maintaining paracellular Na+ permeability for sweat production and kidney function., Author summary Claudins are tight junction proteins forming paracellular barriers that are critical for normal development and homeostasis. The tissue specific paracellular barrier properties are determined by the protein composition of tight junctions that regulates the permeability of solutes and water between different compartments of the body. We show, for the first time, that a mutation in claudin-10b, forming paracellular cation channels in different tissues, causes perturbed Na+ selectivity through altered tight junction formation and function as well as increased degradation of the protein. The mutation is associated with the inability to sweat (anhidrosis) and heat intolerance as well as abnormal cation reabsorption, hypermagnesemia and kidney damage. Our combined findings show that the claudin-10b-mediated paracellular Na+ transport is required for normal sweat production and for the regulation of cation homeostasis in the kidneys.
- Published
- 2017