Wynne, Brandi M. Mistry, Abinash C. Al-Khalili, Otor Mallick, Rickta Theilig, Franziska Eaton, Douglas C. Hoover, Robert S. 2017-06-23 Distal sodium transport is a final step in the regulation of blood pressure. As such, understanding how the two main sodium transport proteins, the thiazide-sensitive sodium chloride cotransporter (NCC) and the epithelial sodium channel (ENaC), are regulated is paramount. Both are expressed in the late distal nephron; however, no evidence has suggested that these two sodium transport proteins interact. Recently, we established that these two sodium transport proteins functionally interact in the second part of the distal nephron (DCT2). Given their co-localization within the DCT2, we hypothesized that NCC and ENaC interactions might be modulated by aldosterone (Aldo). Aldo treatment increased NCC and αENaC colocalization (electron microscopy) and interaction (coimmunoprecipitation). Finally, with co-expression of the Aldo-induced protein serum- and glucocorticoid-inducible kinase 1 (SGK1), NCC and αENaC interactions were increased. These data demonstrate that Aldo promotes increased interaction of NCC and ENaC, within the DCT2 revealing a novel method of regulation for distal sodium reabsorption. application/pdf https://folia.unifr.ch/global/documents/305960 https://folia.unifr.ch/documents/305960/files/the_ama.pdf eng info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-017-03510-5 info:eu-repo/semantics/openAccess License undefined Scientific Reports. - 2017, vol. 7, no. 1, p. 4149 info:eu-repo/classification/udc/57 Aldosterone modulates the association between NCC and ENAC http://purl.org/coar/resource_type/c_6501