Literature DB >> 2472005

Cl- channels in CF: lack of activation by protein kinase C and cAMP-dependent protein kinase.

T C Hwang1, L Lu, P L Zeitlin, D C Gruenert, R Huganir, W B Guggino.   

Abstract

Secretory chloride channels can be activated by adenosine 3',5'-monophosphate (cAMP)-dependent protein kinase in normal airway epithelial cells but not in cells from individuals with cystic fibrosis (CF). In excised, inside-out patches of apical membrane of normal human airway cells and airway cells from three patients with CF, the chloride channels exhibited a characteristic outwardly rectifying current-voltage relation and depolarization-induced activation. Channels from normal tissues were activated by both cAMP-dependent protein kinase and protein kinase C. However, chloride channels from CF patients could not be activated by either kinase. Thus, gating of normal epithelial chloride channels is regulated by both cAMP-dependent protein kinase and protein kinase C, and regulation by both kinases is defective in CF.

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Year:  1989        PMID: 2472005     DOI: 10.1126/science.2472005

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  64 in total

1.  A transformed human epithelial cell line that retains tight junctions post crisis.

Authors:  A L Cozens; M J Yezzi; M Yamaya; D Steiger; J A Wagner; S S Garber; L Chin; E M Simon; G R Cutting; P Gardner
Journal:  In Vitro Cell Dev Biol       Date:  1992 Nov-Dec

2.  CFTR protein expression in primary and cultured epithelia.

Authors:  P L Zeitlin; I Crawford; L Lu; S Woel; M E Cohen; M Donowitz; M H Montrose; A Hamosh; G R Cutting; D Gruenert
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-01       Impact factor: 11.205

3.  Cl- channels in basolateral renal medullary vesicles: V. Comparison of basolateral mTALH Cl- channels with apical Cl- channels from jejunum and trachea.

Authors:  C J Winters; W B Reeves; T E Andreoli
Journal:  J Membr Biol       Date:  1992-05       Impact factor: 1.843

4.  Alternative mRNA splice variants of the rat ClC-2 chloride channel gene are expressed in lung: genomic sequence and organization of ClC-2.

Authors:  S Chu; P L Zeitlin
Journal:  Nucleic Acids Res       Date:  1997-10-15       Impact factor: 16.971

Review 5.  Outwardly rectifying chloride channels and CF: a divorce and remarriage.

Authors:  W B Guggino
Journal:  J Bioenerg Biomembr       Date:  1993-02       Impact factor: 2.945

6.  Effects of the delta F508 mutation on the structure, function, and folding of the first nucleotide-binding domain of CFTR.

Authors:  P J Thomas; P L Pedersen
Journal:  J Bioenerg Biomembr       Date:  1993-02       Impact factor: 2.945

7.  Stimulation of chloride secretion by P1 purinoceptor agonists in cystic fibrosis phenotype airway epithelial cell line CFPEo-.

Authors:  A C Chao; J B Zifferblatt; J A Wagner; Y J Dong; D C Gruenert; P Gardner
Journal:  Br J Pharmacol       Date:  1994-05       Impact factor: 8.739

8.  Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents.

Authors:  S B Fulmer; E M Schwiebert; M M Morales; W B Guggino; G R Cutting
Journal:  Proc Natl Acad Sci U S A       Date:  1995-07-18       Impact factor: 11.205

9.  Protein kinase A-regulated Cl- channel in ML-1 human hematopoietic myeloblasts.

Authors:  B Xu; L Lu
Journal:  J Membr Biol       Date:  1994-10       Impact factor: 1.843

10.  Alterations in a voltage-gated K+ current during the differentiation of ML-1 human myeloblastic leukemia cells.

Authors:  L Lu; T Yang; D Markakis; W B Guggino; R W Craig
Journal:  J Membr Biol       Date:  1993-03       Impact factor: 1.843

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