Interregulation of proton-gated Na(+) channel 3 and cystic fibrosis transmembrane conductance regulator (Q34570321)

3 August 2017

title

Interregulation of proton-gated Na(+) channel 3 and cystic fibrosis transmembrane conductance regulator (English)

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3 August 2017

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transmembrane protein

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7

Eric J Sorscher

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3 August 2017

Estelle Cormet-Boyaka

4

object named as

Estelle Cormet-Boyaka

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3 August 2017

8

Dale J Benos

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3 August 2017

Xuefeng Su

1

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3 August 2017

Qingnan Li

2

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3 August 2017

Kedar Shrestha

3

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3 August 2017

Lan Chen

5

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3 August 2017

Peter R Smith

6

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3 August 2017

Sadis Matalon

9

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3 August 2017

Hong-Long Ji

10

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3 August 2017

language of work or name

English

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publication date

29 September 2006

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Journal of Biological Chemistry

3 August 2017

published in

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volume

281

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3 August 2017

issue

48

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3 August 2017

page(s)

36960-36968

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The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.

3 August 2017

cites work

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The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.

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ENaC is inhibited by an increase in the intracellular Cl(-) concentration mediated through activation of Cl(-) channels

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cAMP-dependent activation of CFTR inhibits the epithelial sodium channel (ENaC) without affecting its surface expression

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Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes.

21 January 2018

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The cytosolic termini of the beta- and gamma-ENaC subunits are involved in the functional interactions between cystic fibrosis transmembrane conductance regulator and epithelial sodium channel

21 January 2018

1 reference

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Cl- transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co-expressing CFTR and ENaC.

21 January 2018

1 reference

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Role of CFTR's PDZ1-binding domain, NBF1 and Cl(-) conductance in inhibition of epithelial Na(+) channels in Xenopus oocytes

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Evidence for reduced Cl- and increased Na+ permeability in cystic fibrosis human primary cell cultures.

21 January 2018

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Downregulation of epithelial sodium channel (ENaC) by CFTR co-expressed in Xenopus oocytes is independent of Cl- conductance

21 January 2018

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Genistein restores functional interactions between Delta F508-CFTR and ENaC in Xenopus oocytes

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H(+)-gated cation channels

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H(+)-gated cation channels: neuronal acid sensors in the NaC/DEG family of ion channels

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Expression of cystic fibrosis transmembrane conductance regulator in rat efferent duct epithelium.

21 January 2018

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Molecular cloning and functional expression of a novel amiloride-sensitive Na+ channel

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Abnormal fluid transport by the epididymis as a cause of obstructive azoospermia

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Pancreatic acinar cell dysfunction in CFTR(-/-) mice is associated with impairments in luminal pH and endocytosis

21 January 2018

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Osmotic water permeabilities of cultured, well-differentiated normal and cystic fibrosis airway epithelia

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Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

21 January 2018

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Exhaled breath condensate pH and exhaled nitric oxide in allergic asthma and in cystic fibrosis

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Molecular cloning of a non-inactivating proton-gated Na+ channel specific for sensory neurons

21 January 2018

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Molecular cloning and regional distribution of a human proton receptor subunit with biphasic functional properties

21 January 2018

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Functional properties and pharmacological inhibition of ASIC channels in the human SJ-RH30 skeletal muscle cell line.

21 January 2018

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Acid-sensing ion channels in malignant gliomas

21 January 2018

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Reactive oxygen nitrogen species decrease cystic fibrosis transmembrane conductance regulator expression and cAMP-mediated Cl- secretion in airway epithelia

21 January 2018

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Up-regulation of acid-gated Na(+) channels (ASICs) by cystic fibrosis transmembrane conductance regulator co-expression in Xenopus oocytes

21 January 2018

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Chemical gating of gap junction channels; roles of calcium, pH and calmodulin

21 January 2018

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A small molecule CFTR inhibitor produces cystic fibrosis-like submucosal gland fluid secretions in normal airways

21 January 2018

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Hyposecretion, not hyperabsorption, is the basic defect of cystic fibrosis airway glands

21 January 2018

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21 January 2018

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Delta-subunit confers novel biophysical features to alpha beta gamma-human epithelial sodium channel (ENaC) via a physical interaction

21 January 2018

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pH Dependency and desensitization kinetics of heterologously expressed combinations of acid-sensing ion channel subunits

21 January 2018

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Regulation of channel gating by AMP-activated protein kinase modulates cystic fibrosis transmembrane conductance regulator activity in lung submucosal cells

21 January 2018

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Regulation of intracellular pH in Calu-3 human airway cells

21 January 2018

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Endogenous airway acidification. Implications for asthma pathophysiology

21 January 2018

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Degenerin sites mediate proton activation of deltabetagamma-epithelial sodium channel

21 January 2018

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Duodenal pH in cystic fibrosis and its relationship to fat malabsorption

21 January 2018

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Na+ and Cl? conductances in airway epithelial cells: increased Na+ conductance in cystic fibrosis

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M608002200

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3 August 2017

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