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CMP
Credit: Jack Hobhouse

Professor Stephen Tucker

Professor of Biophysics

Research theme

  • Biological physics

Sub department

  • Condensed Matter Physics

Research groups

  • Ion channels
Stephen.Tucker@physics.ox.ac.uk
Telephone: 01865 (2)72382
Biochemistry Building, room 30-090 Kavli Institute, DCHB
  • About
  • Publications

The Kir5.1 Potassium Channel is an Important Determinant of Neuronal PCO2/pH Sensitivity

Biophysical Journal Elsevier 100:3 (2011) 430a

Authors:

M Cristina D'Adamo, Lijun Shang, Paola Imbrici, Steve DM Brown, Mauro Pessia, Stephen J Tucker
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Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity.

The Journal of biological chemistry 286:1 (2011) 192-198

Authors:

M Cristina D'Adamo, Lijun Shang, Paola Imbrici, Steve DM Brown, Mauro Pessia, Stephen J Tucker

Abstract:

The molecular identity of ion channels which confer PCO(2)/pH sensitivity in the brain is unclear. Heteromeric Kir4.1/Kir5.1 channels are highly sensitive to inhibition by intracellular pH and are widely expressed in several brainstem nuclei involved in cardiorespiratory control, including the locus coeruleus. This has therefore led to a proposed role for these channels in neuronal CO(2) chemosensitivity. To examine this, we generated mutant mice lacking the Kir5.1 (Kcnj16) gene. We show that although locus coeruleus neurons from Kcnj16((+/+)) mice rapidly respond to cytoplasmic alkalinization and acidification, those from Kcnj16((-/-)) mice display a dramatically reduced and delayed response. These results identify Kir5.1 as an important determinant of PCO(2)/pH sensitivity in locus coeruleus neurons and suggest that Kir5.1 may be involved in the response to hypercapnic acidosis.
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Genetic Inactivation of Kcnj16 Identifies Kir5.1 as an Important Determinant of Neuronal PCO2/pH Sensitivity

JOURNAL OF BIOLOGICAL CHEMISTRY 286:1 (2011) 192-198

Authors:

M Cristina D'Adamo, Lijun Shang, Paola Imbrici, Steve DM Brown, Mauro Pessia, Stephen J Tucker
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Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndrome

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 108:25 (2011) 10361-10366

Authors:

Marc Paulais, May Bloch-Faure, Nicolas Picard, Thibaut Jacques, Suresh Krishna Ramakrishnan, Mathilde Keck, Fabien Sohet, Dominique Eladari, Pascal Houillier, Stephane Lourdel, Jacques Teulon, Stephen J Tucker
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Respiratory responses to hypercapnia and hypoxia in mice with genetic ablation of Kir5.1 (Kcnj16)

EXPERIMENTAL PHYSIOLOGY 96:4 (2011) 451-459

Authors:

Stefan Trapp, Stephen J Tucker, Alexander V Gourine
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