Open AccessEvidence for a regulated Ca2+ entry in proximal tubular cells and its implication in calcium stone formation
Author(s) -
Cliff Lawrence Ibeh,
Allen J. Yiu,
Yianni L. Kanaras,
Edina Paal,
Lutz Birnbaumer,
Pedro A. José,
Bidhan C. Bandyopadhyay
Publication year - 2019
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.225268
Subject(s) - trpc3 , transcellular , reabsorption , biology , paracellular transport , calcium , microbiology and biotechnology , transient receptor potential channel , biophysics , receptor , trpc , membrane , medicine , biochemistry , kidney , endocrinology , permeability (electromagnetism)
Calcium phosphate (CaP) crystals, which begin to form in the early segments of the loop of Henle (LOH), are known to act as precursors for calcium stone formation. Proximal tubule (PT), just upstream to LOH, a major site for Ca2+ reabsorption, could be a regulator to such CaP crystal formation. However, PT Ca2+ reabsorption is mostly described as paracellular. Here we show the existence of a regulated transcellular Ca2+ entry pathway in luminal membrane PT cells induced by Ca2+-sensing receptor (CSR) activation of transient receptor potential canonical 3 (TRPC3). In support, we found that both CSR and TRPC3 are physically and functionally coupled at the luminal membrane of PT cells. More importantly, TRPC3 deficient mice presented with a deficiency in PT Ca2+ entry/transport, elevated urinary [Ca2+], microcalcifications in LOH, and urine microcrystals formations. Together these data suggest that a signaling complex comprising of CSR and TRPC3 exists in the PT and can mediate transcellular Ca2+ transport, which could be critical in maintaining the PT luminal [Ca2+] to mitigate the CaP crystals in LOH and hence can hinder calcium stone formation.