Pubblicazioni

Autori:

Su, W.; Shmukler, B. E.; Chernova, M. N.; Stuart-Tilley, A. K.; De Franceschi, L.; Brugnara, C.; Alper, S. L.

Titolo:

Mouse K-Cl cotransporte KCC1: cloning, mapping, pathological expression and functional regulation.

Anno:

1999

Tipologia prodotto:

Articolo in Rivista

Tipologia ANVUR:

Articolo su rivista

Lingua:

Inglese

Formato:

A Stampa

Referee:

Sì

Nome rivista:

American Journal of Physiology

ISSN Rivista:

0002-9513

N° Volume:

277

Numero o Fascicolo:

5

Editore:

American Journal of Physiology

Intervallo pagine:

C899-C912

Parole chiave:

Red blood cells; SAD1; SC disease; Sickle cell disease; Thalassemia

Breve descrizione dei contenuti:

Although K-Cl cotransporter (KCC1) mRNA is expressed in many tissues, K-Cl cotransport activity has been measured in few cell types, and detection of endogenous KCC1 polypeptide has not yet been reported. We have cloned the mouse erythroid KCC1 (mKCC1) cDNA and its flanking genomic regions and mapped the mKCC1 gene to chromosome 8. Three anti-peptide antibodies raised against recombinant mKCC1 function as immunoblot and immunoprecipitation reagents. The tissue distributions of mKCC1 mRNA and protein are widespread, and mKCC1 RNA is constitutively expressed during erythroid differentiation of ES cells. KCC1 polypeptide or related antigen is present in erythrocytes of multiple species in which K-Cl cotransport activity has been documented. Erythroid KCC1 polypeptide abundance is elevated in proportion to reticulocyte counts in density-fractionated cells, in bleeding-induced reticulocytosis, in mouse models of sickle cell disease and thalassemia, and in the corresponding human disorders. mKCC1-mediated uptake of (86)Rb into Xenopus oocytes requires extracellular Cl(-), is blocked by the diuretic R(+)-[2-n-butyl-6,7-dichloro-2-cyclopentyl-2, 3-dihydro-1-oxo-1H-indenyl-5-yl-)oxy]acetic acid, and exhibits an erythroid pattern of acute regulation, with activation by hypotonic swelling, N-ethylmaleimide, and staurosporine and inhibition by calyculin and okadaic acid. These reagents and findings will expedite studies of KCC1 structure-function relationships and of the pathobiology of KCC1-mediated K-Cl cotransport.

Pagina Web:

https://doi.org/10.1152/ajpcell.1999.277.5.c899

Id prodotto:

424

Handle IRIS:

11562/424

depositato il:

28 novembre 2007

ultima modifica:

15 novembre 2022

Citazione bibliografica:

Su, W.; Shmukler, B. E.; Chernova, M. N.; Stuart-Tilley, A. K.; De Franceschi, L.; Brugnara, C.; Alper, S. L., Mouse K-Cl cotransporte KCC1: cloning, mapping, pathological expression and functional regulation. «American Journal of Physiology» , vol. 277 , n. 5 , 1999 , pp. C899-C912

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