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Colonic H-K-ATPase beta -subunit: identification in apical membranes and regulation by dietary K depletion
Authors:Sangan  Pitchai; Kolla  Sarah S; Rajendran  Vazhaikkurichi M; Kashgarian  Michael; Binder  Henry J
Abstract:P-type ATPasesrequire both alpha - and beta -subunits for functionalactivity. Although an alpha -subunit for colonic apical membraneH-K-ATPase (HKcalpha ) has been identified and studied, its beta -subunithas not been identified. We cloned putative beta -subunit rat colonicH-K-ATPase (HKcbeta ) cDNA that encodes a 279-amino-acid protein with asingle transmembrane domain and sequence homology to other ratbeta -subunits. Northern blot analysis demonstrates that this HKcbeta isexpressed in several rat tissues, including distal and proximal colon,and is highly expressed in testis and lung. HKcbeta mRNA abundance is upregulated threefold compared with normal in distal colon but notproximal colon, testis, or lung of K-depleted rats. In contrast, Na-K-ATPase beta 1 mRNA abundance isunaltered in distal colon of K-depleted rats. Na depletion, which alsostimulates active K absorption in distal colon, does not increaseHKcbeta mRNA abundance. Western blot analyses using a polyclonalantibody raised to a glutathioneS-transferase-HKcbeta fusion proteinestablished expression of a 45-kDa HKcbeta protein in both apical andbasolateral membranes of rat distal colon, but K depletion increasedHKcbeta protein expression only in apical membranes. Physicalassociation between HKcbeta and HKcalpha proteins was demonstrated byWestern blot analysis performed with HKcbeta antibody onimmunoprecipitate of apical membranes of rat distal colon and HKcalpha antibody. Tissue-specific upregulation of this beta -subunit mRNA inresponse to K depletion, localization of its protein, its upregulationby K depletion in apical membranes of distal colon, and its physicalassociation with HKcalpha protein provide compelling evidence that HKcbeta is the putative beta -subunit of colonic H-K-ATPase.
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