Asthma is a chronic inflammatory disease of the airways whose global prevalence has taken on pandemic proportions. Although research has made great strides in elucidating the underlying mechanisms involved in asthma, in recent decades relatively few new additions have been made to the pharmacological armamentarium for this disease. Our laboratory has made several novel discoveries: (1) that 3-aminobutyric acid subtype A (GABAA) GABAA receptors are expressed on airway smooth muscle cells, (2) that an endogenous GABAergic ligand-receptor system exists in the airway, (3) that activation of endogenous airway smooth muscle GABAA receptors potentiates relaxation, (4) that GABA (endogenously present in the airway) functions to modulate airway smooth muscle tone, (5) that systemic administration of a GABAA receptor agonist administered in vivo attenuates agonist-induced airway constriction and that (6) part of propofol's broncho-relaxant effect is mediated by GABAA receptors on airway smooth muscle. Since pharmacologic specificity of ligands/agonists directed at the GABAA receptor is dictated by GABAA subunit composition, selective targeting of certain subunits restricted to a given tissue hold promise for improved therapy. Therefore, our goal is to elucidate the importance of airway smooth muscle GABAA receptor subunit composition on the modulation of airway smooth muscle tone. We previously demonstrated that human airway smooth muscle expresses a limited, yet highly conserved repertoire of GABAA receptor subunits (including 14, 15, 23, 32 and 42. This limited repertoire of subunits is advantageous, as it may allow for highly selective targeting of GABAA ) receptors expressed on airway smooth muscle. Exciting preliminary data generated for this proposal support the central hypothesis that airway epithelium is an important cellular source for airway GABA. It is released from epithelial cells via kinase- regulated GABA transporters (GAT2 and GAT4/BGT-1) to act upon 14- and/or 15 containing GABAA receptors on airway smooth muscle cells to facilitate relaxation. These findings offer a radical new therapy, a translational therapeutic approach and a novel paradigm for paracrine interactions between airway epithelium and smooth muscle for relaxing airway constriction.
The central hypotheses to be addressed by the studies are that airway epithelium is a cellular source for airway GABA that is released from epithelial cells via kinase-regulated GABA transporters (GAT2 and GAT4/BGT-1). This released GABA can then act upon 14- and/or 15 containing GABAA receptors on airway smooth muscle cells to facilitate relaxation. We plan to identify novel 14 or 15 subunit-selective agonists that can be delivered to airways by aerosol to facilitate airway relaxation. These findings offer a radical new therapy, a translational therapeutic approach and a novel paradigm for paracrine interactions between airway epithelium and smooth muscle for relaxing airway constriction.
|Townsend, Elizabeth A; Zhang, Yi; Xu, Carrie et al. (2014) Active components of ginger potentiate *-agonist-induced relaxation of airway smooth muscle by modulating cytoskeletal regulatory proteins. Am J Respir Cell Mol Biol 50:115-24|
|Danielsson, Jennifer; Yim, Peter; Rinderspacher, Alison et al. (2014) Chloride channel blockade relaxes airway smooth muscle and potentiates relaxation by ?-agonists. Am J Physiol Lung Cell Mol Physiol 307:L273-82|
|Townsend, Elizabeth A; Siviski, Matthew E; Zhang, Yi et al. (2013) Effects of ginger and its constituents on airway smooth muscle relaxation and calcium regulation. Am J Respir Cell Mol Biol 48:157-63|
|Mizuta, Kentaro; Zhang, Yi; Xu, Dingbang et al. (2013) The dopamine D1 receptor is expressed and facilitates relaxation in airway smooth muscle. Respir Res 14:89|
|Gallos, George; Townsend, Elizabeth; Yim, Peter et al. (2013) Airway epithelium is a predominant source of endogenous airway GABA and contributes to relaxation of airway smooth muscle tone. Am J Physiol Lung Cell Mol Physiol 304:L191-7|
|Townsend, Elizabeth A; Emala Sr, Charles W (2013) Quercetin acutely relaxes airway smooth muscle and potentiates ?-agonist-induced relaxation via dual phosphodiesterase inhibition of PLC? and PDE4. Am J Physiol Lung Cell Mol Physiol 305:L396-403|
|Gallos, George; Remy, Kenneth E; Danielsson, Jennifer et al. (2013) Functional expression of the TMEM16 family of calcium-activated chloride channels in airway smooth muscle. Am J Physiol Lung Cell Mol Physiol 305:L625-34|
|Gallos, George; Yim, Peter; Chang, Sucie et al. (2012) Targeting the restricted ?-subunit repertoire of airway smooth muscle GABAA receptors augments airway smooth muscle relaxation. Am J Physiol Lung Cell Mol Physiol 302:L248-56|
|Mizuta, Kentaro; Zhang, Yi; Xu, Dingbang et al. (2012) The dopamine D(2) receptor is expressed and sensitizes adenylyl cyclase activity in airway smooth muscle. Am J Physiol Lung Cell Mol Physiol 302:L316-24|
|Xu, Alice; Prophete, Colette; Chen, Lung-chi et al. (2011) Interactive effect of cigarette smoke extract and world trade center dust particles on airway cell cytotoxicity. J Toxicol Environ Health A 74:887-902|
Showing the most recent 10 out of 21 publications