Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits.


Autoria(s): Canessa C.M.; Schild L.; Buell G.; Thorens B.; Gautschi I.; Horisberger J.D.; Rossier B.C.
Data(s)

01/02/1994

Resumo

The amiloride-sensitive epithelial sodium channel constitutes the rate-limiting step for sodium reabsorption in epithelial cells that line the distal part of the renal tubule, the distal colon, the duct of several exocrine glands, and the lung. The activity of this channel is upregulated by vasopressin and aldosterone, hormones involved in the maintenance of sodium balance, blood volume and blood pressure. We have identified the primary structure of the alpha-subunit of the rat epithelial sodium channel by expression cloning in Xenopus laevis oocytes. An identical subunit has recently been reported. Here we identify two other subunits (beta and gamma) by functional complementation of the alpha-subunit of the rat epithelial Na+ channel. The ion-selective permeability, the gating properties and the pharmacological profile of the channel formed by coexpressing the three subunits in oocytes are similar to that of the native channel.

Identificador

http://serval.unil.ch/?id=serval:BIB_7C59A7C33DB2

isbn:0028-0836

pmid:8107805

doi:10.1038/367463a0

isiid:A1994MU67900055

Idioma(s)

en

Fonte

Nature, vol. 367, no. 6462, pp. 463-467

Palavras-Chave #Amiloride; Amino Acid Sequence; Animals; Cell Line; Cells, Cultured; Epithelium; Ion Channel Gating; Membrane Potentials; Molecular Sequence Data; Oocytes; Permeability; Rats; Recombinant Proteins; Sodium Channels; Xenopus laevis
Tipo

info:eu-repo/semantics/article

article