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CaMKII is essential for the proasthmatic effects of oxidation

CaMKII is essential for the proasthmatic effects of oxidation
CaMKII is essential for the proasthmatic effects of oxidation
Increased reactive oxygen species (ROS) contribute to asthma, but little is known about the molecular mechanisms connecting increased ROS with characteristic features of asthma. We show that enhanced oxidative activation of the Ca(2+)/calmodulin-dependent protein kinase (ox-CaMKII) in bronchial epithelium positively correlates with asthma severity and that epithelial ox-CaMKII increases in response to inhaled allergens in patients. We used mouse models of allergic airway disease induced by ovalbumin (OVA) or Aspergillus fumigatus (Asp) and found that bronchial epithelial ox-CaMKII was required to increase a ROS- and picrotoxin-sensitive Cl(-) current (ICl) and MUC5AC expression, upstream events in asthma progression. Allergen challenge increased epithelial ROS by activating NADPH oxidases. Mice lacking functional NADPH oxidases due to knockout of p47 and mice with epithelial-targeted transgenic expression of a CaMKII inhibitory peptide or wild-type mice treated with inhaled KN-93, an experimental small-molecule CaMKII antagonist, were protected against increases in ICl, MUC5AC expression, and airway hyperreactivity to inhaled methacholine. Our findings support the view that CaMKII is a ROS-responsive, pluripotent proasthmatic signal and provide proof-of-concept evidence that CaMKII is a therapeutic target in asthma.
1946-6234
195ra97
Sanders, Philip N.
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Koval, Olha M.
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Jaffer, Omar A.
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Prasad, Anand M.
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Businga, Thomas R.
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Scott, Jason A.
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Hayden, Patrick J.
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Luczak, Elizabeth D.
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Dickey, David D.
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Allamargot, Chantal
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Olivier, Alicia K.
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Meyerholz, David K.
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Robison, Alfred J.
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Winder, Danny G.
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Blackwell, Timothy S.
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Dworski, Ryszard
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Sammut, David
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Wagner, Brett A.
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Buettner, Garry R.
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Pope, Robert M.
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Miller, Francis J.
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Dibbern, Megan E.
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Haitchi, Hans Michael
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Mohler, Peter J.
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Howarth, Peter H.
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Zabner, Joseph
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Kline, Joel N.
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Grumbach, Isabella M.
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Anderson, Mark E.
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Sanders, Philip N.
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Koval, Olha M.
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Jaffer, Omar A.
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Prasad, Anand M.
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Businga, Thomas R.
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Scott, Jason A.
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Luczak, Elizabeth D.
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Dickey, David D.
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Allamargot, Chantal
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Olivier, Alicia K.
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Meyerholz, David K.
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Robison, Alfred J.
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Winder, Danny G.
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Blackwell, Timothy S.
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Dworski, Ryszard
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Sammut, David
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Wagner, Brett A.
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Buettner, Garry R.
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Pope, Robert M.
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Miller, Francis J.
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Dibbern, Megan E.
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Haitchi, Hans Michael
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Mohler, Peter J.
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Howarth, Peter H.
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Zabner, Joseph
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Kline, Joel N.
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Grumbach, Isabella M.
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Anderson, Mark E.
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Sanders, Philip N., Koval, Olha M., Jaffer, Omar A., Prasad, Anand M., Businga, Thomas R., Scott, Jason A., Hayden, Patrick J., Luczak, Elizabeth D., Dickey, David D., Allamargot, Chantal, Olivier, Alicia K., Meyerholz, David K., Robison, Alfred J., Winder, Danny G., Blackwell, Timothy S., Dworski, Ryszard, Sammut, David, Wagner, Brett A., Buettner, Garry R., Pope, Robert M., Miller, Francis J., Dibbern, Megan E., Haitchi, Hans Michael, Mohler, Peter J., Howarth, Peter H., Zabner, Joseph, Kline, Joel N., Grumbach, Isabella M. and Anderson, Mark E. (2013) CaMKII is essential for the proasthmatic effects of oxidation. Science Translational Medicine, 5 (195), 195ra97. (doi:10.1126/scitranslmed.3006135). (PMID:23884469)

Record type: Article

Abstract

Increased reactive oxygen species (ROS) contribute to asthma, but little is known about the molecular mechanisms connecting increased ROS with characteristic features of asthma. We show that enhanced oxidative activation of the Ca(2+)/calmodulin-dependent protein kinase (ox-CaMKII) in bronchial epithelium positively correlates with asthma severity and that epithelial ox-CaMKII increases in response to inhaled allergens in patients. We used mouse models of allergic airway disease induced by ovalbumin (OVA) or Aspergillus fumigatus (Asp) and found that bronchial epithelial ox-CaMKII was required to increase a ROS- and picrotoxin-sensitive Cl(-) current (ICl) and MUC5AC expression, upstream events in asthma progression. Allergen challenge increased epithelial ROS by activating NADPH oxidases. Mice lacking functional NADPH oxidases due to knockout of p47 and mice with epithelial-targeted transgenic expression of a CaMKII inhibitory peptide or wild-type mice treated with inhaled KN-93, an experimental small-molecule CaMKII antagonist, were protected against increases in ICl, MUC5AC expression, and airway hyperreactivity to inhaled methacholine. Our findings support the view that CaMKII is a ROS-responsive, pluripotent proasthmatic signal and provide proof-of-concept evidence that CaMKII is a therapeutic target in asthma.

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More information

Accepted/In Press date: 5 June 2013
Published date: 24 July 2013
Organisations: Clinical & Experimental Sciences

Identifiers

Local EPrints ID: 359021
URI: http://eprints.soton.ac.uk/id/eprint/359021
ISSN: 1946-6234
PURE UUID: 48ed110c-6762-48c7-94cf-8a888c43fa5c
ORCID for Hans Michael Haitchi: ORCID iD orcid.org/0000-0001-8603-302X

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Date deposited: 18 Oct 2013 13:15
Last modified: 15 Mar 2024 03:14

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Contributors

Author: Philip N. Sanders
Author: Olha M. Koval
Author: Omar A. Jaffer
Author: Anand M. Prasad
Author: Thomas R. Businga
Author: Jason A. Scott
Author: Patrick J. Hayden
Author: Elizabeth D. Luczak
Author: David D. Dickey
Author: Chantal Allamargot
Author: Alicia K. Olivier
Author: David K. Meyerholz
Author: Alfred J. Robison
Author: Danny G. Winder
Author: Timothy S. Blackwell
Author: Ryszard Dworski
Author: David Sammut
Author: Brett A. Wagner
Author: Garry R. Buettner
Author: Robert M. Pope
Author: Francis J. Miller
Author: Megan E. Dibbern
Author: Peter J. Mohler
Author: Joseph Zabner
Author: Joel N. Kline
Author: Isabella M. Grumbach
Author: Mark E. Anderson

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