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Am J Physiol Lung Cell Mol Physiol (February 28, 2003). doi:10.1152/ajplung.00322.2002
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Submitted on September 25, 2002
Accepted on February 24, 2003

Methacholine-induced airway hyperresponsiveness is dependent on G{alpha}q signaling

Michael T. Borchers1, Travis Biechele1, Joshua P. Justice1, Tracy L. Ansay1, Stephania Cornier1, Valeria Mancino2, Thomas M. Wilkie3, Melvin I. Simon2, Nancy A. Lee1, and James J. Lee1*

1 Department of Biochemistry and Molecular Biology, Mayo Clinic, Scottsdale, AZ, USA
2 Division of Biology, California Institute of Technology, Pasadena, CA, USA
3 Department of Pharmacology, UT Southwestern, Dallas, TX, USA

* To whom correspondence should be addressed. E-mail: jlee{at}mayo.edu.

Airway function in health and disease as well as in response to bronchospastic stimuli (i.e., irritants, allergens and inflammatory mediators) is controlled, in part, by cholinergic muscarinic receptor regulation of smooth muscle. In particular, the dependence of airway smooth muscle contraction/relaxation on heterotrimeric G protein-coupled receptor signaling suggests that these events underlie the responses regulating airway function. G{alpha}q containing G-proteins are proposed to be a prominent signaling pathway and the availability of knockout mice deficient of this subunit has allowed for an investigation of its potential role in airway function. Airway responses in G{alpha}q deficient mice, assessing activity by both tracheal tension and in vivo lung function measurements, were attenuated relative to wild type controls. Moreover, ovalbumin sensitization/aerosol challenge of G{alpha}q deficient mice also failed to elicit an allergen-induced increase in airway reactivity to methacholine. These findings indicate that cholinergic receptor mediated responses are dependent on G{alpha}q-mediated signaling events and identifies G{alpha}q as a potential target of preventative/intervening therapies for lung dysfunction.




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