Function of FXYD proteins, regulators of Na, K-ATPase

Détails

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Etat: Public
Version: Final published version
Licence: Non spécifiée
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ID Serval
serval:BIB_E0189E3CC770
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Function of FXYD proteins, regulators of Na, K-ATPase
Périodique
Journal of Bioenergetics and Biomembranes
Auteur⸱e⸱s
Geering  K.
ISSN
0145-479X (Print)
Statut éditorial
Publié
Date de publication
12/2005
Volume
37
Numéro
6
Pages
387-92
Notes
Journal Article
Research Support, Non-U.S. Gov't
Review --- Old month value: Dec
Résumé
In this short review, we summarize our work on the role of members of the FXYD protein family as tissue-specific modulators of Na, K-ATPase. FXYD1 or phospholemman, mainly expressed in heart and skeletal muscle increases the apparent affinity for intracellular Na(+) of Na, K-ATPase and may thus be important for appropriate muscle contractility. FXYD2 or gamma subunit and FXYD4 or CHIF modulate the apparent affinity for Na(+) of Na, K-ATPase in an opposite way, adapted to the physiological needs of Na(+) reabsorption in different segments of the renal tubule. FXYD3 expressed in stomach, colon, and numerous tumors also modulates the transport properties of Na, K-ATPase but it has a lower specificity of association than other FXYD proteins and an unusual membrane topology. Finally, FXYD7 is exclusively expressed in the brain and decreases the apparent affinity for extracellular K(+), which may be essential for proper neuronal excitability.
Mots-clé
Animals *Homeostasis Humans Intracellular Signaling Peptides and Proteins Membrane Glycoproteins Membrane Proteins Na(+)-K(+)-Exchanging ATPase/*physiology Neoplasm Proteins Nerve Tissue Proteins Organ Specificity Phosphoproteins Potassium Channels
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/01/2008 13:28
Dernière modification de la notice
14/02/2022 8:57
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