Literature DB >> 16757733

Locations, abundances, and possible functions of FXYD ion transport regulators in rat renal medulla.

Kaarina Pihakaski-Maunsbach1, Henrik Vorum, Bent Honoré, Shigeki Tokonabe, Jørgen Frøkiaer, Haim Garty, Steven J D Karlish, Arvid B Maunsbach.   

Abstract

The gamma-subunit of Na-K-ATPase (FXYD2) and corticosteroid hormone-induced factor (CHIF; FXYD4) are considered pump regulators in kidney tubules. The aim of this study was to expand the information about their locations in the kidney medulla and to evaluate their importance for electrolyte excretion in an animal model. The cellular and subcellular locations and abundances of gamma and CHIF in the medulla of control and sodium-depleted rats were analyzed by immunofluorescence and immunoelectron microscopy and semiquantitative Western blotting. The results showed that antibodies against the gamma-subunit COOH terminus and splice variant gamma(a), but not splice variant gamma(b), labeled intercalated cells, but not principal cells, in the initial part of the inner medullary collecting duct (IMCD1). In subsequent segments (IMCD2 and IMCD3), all principal cells exhibited distinct basolateral labeling for both the gamma-subunit COOH terminus, splice variant gamma(a), and CHIF. Splice variant gamma(b) was abundant in the inner stripe of the outer medulla but absent in the inner medulla (IM). Double labeling by high-resolution immunoelectron microscopy showed close structural association between CHIF and the Na-K-ATPase alpha(1)-subunit in basolateral membranes. The present observations provide new information about the cellular and subcellular locations of gamma and CHIF in the renal medulla and show a new gamma variant in the IM. Extensive NaCl depletion did not induce significant changes in the locations or abundances of the gamma-subunit COOH terminus and CHIF in different kidney zones. We conclude that the unchanged levels of these two FXYD proteins suggest that they are not primary determinants for urine electrolyte composition during NaCl depletion.

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Year:  2006        PMID: 16757733     DOI: 10.1152/ajprenal.00086.2006

Source DB:  PubMed          Journal:  Am J Physiol Renal Physiol        ISSN: 1522-1466


  6 in total

1.  Post-transcriptional control of Na,K-ATPase activity and cell growth by a splice variant of FXYD2 protein with modified mRNA.

Authors:  Kathleen J Sweadner; Jennifer L Pascoa; Cynthia A Salazar; Elena Arystarkhova
Journal:  J Biol Chem       Date:  2011-04-01       Impact factor: 5.157

2.  FXYD proteins stabilize Na,K-ATPase: amplification of specific phosphatidylserine-protein interactions.

Authors:  Neeraj Kumar Mishra; Yoav Peleg; Erica Cirri; Talya Belogus; Yael Lifshitz; Dennis R Voelker; Hans-Juergen Apell; Haim Garty; Steven J D Karlish
Journal:  J Biol Chem       Date:  2011-01-12       Impact factor: 5.157

3.  Structure of the Na,K-ATPase regulatory protein FXYD2b in micelles: implications for membrane-water interfacial arginines.

Authors:  Xiao-Min Gong; Yi Ding; Jinghua Yu; Yong Yao; Francesca M Marassi
Journal:  Biochim Biophys Acta       Date:  2014-05-02

Review 4.  Molecular determinants of magnesium homeostasis: insights from human disease.

Authors:  R Todd Alexander; Joost G Hoenderop; René J Bindels
Journal:  J Am Soc Nephrol       Date:  2008-06-18       Impact factor: 10.121

5.  FXYD proteins and sodium pump regulatory mechanisms.

Authors:  John Q Yap; Jaroslava Seflova; Ryan Sweazey; Pablo Artigas; Seth L Robia
Journal:  J Gen Physiol       Date:  2021-04-05       Impact factor: 4.086

6.  Expression and trafficking of the gamma subunit of Na,K-ATPase in hypertonically challenged IMCD3 cells.

Authors:  Kaarina Pihakaski-Maunsbach; Shoichi Nonaka; Arvid B Maunsbach
Journal:  Acta Histochem Cytochem       Date:  2008-08-28       Impact factor: 1.938

  6 in total

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