Literature DB >> 17434346

CFTR stabilizes ENaC at the plasma membrane.

C Lu1, C Jiang, S Pribanic, D Rotin.   

Abstract

CFTR was reported to regulate ENaC channel opening, decreasing ENaC activity in airways and increasing it in sweat ducts. We generated MDCK-I cell lines stably expressing tagged alphabetagammaENaC+CFTR or ENaC alone, and developed an assay to quantify cell-surface half-life of ENaC. Surprisingly, we found that co-expressed CFTR stabilizes ENaC at the plasma membrane, suggesting that CFTR regulates ENaC stability, not just opening.

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Year:  2007        PMID: 17434346     DOI: 10.1016/j.jcf.2007.03.001

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  7 in total

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Review 4.  Liquid movement across the surface epithelium of large airways.

Authors:  Lucy A Chambers; Brett M Rollins; Robert Tarran
Journal:  Respir Physiol Neurobiol       Date:  2007-06-17       Impact factor: 1.931

Review 5.  Cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis: current perspectives.

Authors:  Béla Z Schmidt; Jérémy B Haaf; Teresinha Leal; Sabrina Noel
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Review 6.  Cystic fibrosis as a bowel cancer syndrome and the potential role of CK2.

Authors:  Anil Mehta
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7.  ESCRT regulates surface expression of the Kir2.1 potassium channel.

Authors:  Alexander R Kolb; Patrick G Needham; Cari Rothenberg; Christopher J Guerriero; Paul A Welling; Jeffrey L Brodsky
Journal:  Mol Biol Cell       Date:  2013-11-13       Impact factor: 4.138

  7 in total

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