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Biased TAS2R Bronchodilators Inhibit Airway Smooth Muscle Growth by Downregulating Phosphorylated Extracellular Signal-regulated Kinase 1/2.
Kim, Donghwa; Cho, Soomin; Castaño, Maria A; Panettieri, Reynold A; Woo, Jung A; Liggett, Stephen B.
Afiliación
  • Kim D; 1 Department of Medicine and.
  • Cho S; 2 Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, California; and.
  • Castaño MA; 1 Department of Medicine and.
  • Panettieri RA; 3 Rutgers Institute for Translational Medicine and Science, Robert Wood Johnson Medical School, Rutgers, The State University of New Jersey, New Brunswick, New Jersey.
  • Woo JA; 4 Department of Molecular Pharmacology and Physiology, University of South Florida Morsani College of Medicine, Tampa, Florida.
  • Liggett SB; 1 Department of Medicine and.
Am J Respir Cell Mol Biol ; 60(5): 532-540, 2019 05.
Article en En | MEDLINE | ID: mdl-30365340
Bitter taste receptor (TAS2R) agonists dilate airways by receptor-dependent smooth muscle relaxation. Besides their coupling to relaxation, we have found that human airway smooth muscle (HASM) cell TAS2Rs activate (phosphorylate) extracellular signal-related kinase 1/2 (ERK1/2), but the cellular effects are not known. In the present study, we show in HASM cells that TAS2R agonists initially stimulate phosphorylated ERK1/2 (pERK1/2) but by 24 hours cause a marked (50-70%) downregulation of pERK1/2 without a change in total ERK1/2. It was hypothesized that TAS2R agonists suppress cell growth through this pERK1/2 downregulation. Agonist-dependent inhibition of cell proliferation was indeed found in HASM cells derived from normal and asthmatic human lungs, as well as in an immortalized HASM cell line. pERK1/2 downregulation was linked to downregulation of the upstream kinase MEK1/2 (mitogen-activated protein kinase/extracellular signal-regulated kinase). Various structurally diverse TAS2R agonists evoked a range of inhibition of HASM proliferation, the magnitude of which directly correlated with the downregulation of pERK1/2 (R2 = 0.86). Some TAS2R agonists were as effective as pharmacological inhibitors of Raf1 and MEK1/2 in suppressing growth. siRNA silencing of TAS2Rs (subtypes 10, 14, and 31) ablated the pERK1/2 and growth-inhibitory effects of TAS2R agonists. These phenotypes were attenuated by inhibiting the TAS2R G protein Gαi and by knocking down ß-arrestin 1/2, indicating a dual pathway, although there may be additional mechanisms involved in this HASM TAS2R multidimensional signaling. Thus, TAS2R agonist structure can be manipulated to maintain the relaxation response and can be biased toward suppression of HASM growth. The latter response is of potential therapeutic benefit in asthma, in which an increase in smooth muscle mass contributes to airway obstruction.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Broncodilatadores / Regulación de la Expresión Génica / Proteína Quinasa 1 Activada por Mitógenos / Miocitos del Músculo Liso / Receptores Acoplados a Proteínas G / Proteína Quinasa 3 Activada por Mitógenos Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Am J Respir Cell Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Broncodilatadores / Regulación de la Expresión Génica / Proteína Quinasa 1 Activada por Mitógenos / Miocitos del Músculo Liso / Receptores Acoplados a Proteínas G / Proteína Quinasa 3 Activada por Mitógenos Tipo de estudio: Observational_studies / Risk_factors_studies Idioma: En Revista: Am J Respir Cell Mol Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos