Prolonged heterologous β2-adrenoceptor desensitization promotes proasthmatic airway smooth muscle function via PKA/ERK1/2-mediated phosphodiesterase-4 induction
| Autor: | Judith S. Grunstein, Michael M. Grunstein, Sumbul Fatma, Aihua Hu, Gustavo Nino |
|---|---|
| Rok vydání: | 2008 |
| Předmět: |
Pulmonary and Respiratory Medicine
medicine.medical_specialty Cell signaling Physiology G protein Muscle Relaxation Biology Dinoprostone Receptors G-Protein-Coupled chemistry.chemical_compound Downregulation and upregulation Physiology (medical) Internal medicine Nitriles Butadienes Cyclic AMP medicine Animals Humans Cyclic AMP Response Element-Binding Protein Receptor Adrenergic beta-2 Receptor Agonists Cells Cultured Mitogen-Activated Protein Kinase 1 Sulfonamides Mitogen-Activated Protein Kinase 3 Forskolin Colforsin Phosphodiesterase Cell Biology respiratory system Isoquinolines musculoskeletal system Cyclic AMP-Dependent Protein Kinases Asthma Cyclic Nucleotide Phosphodiesterases Type 4 Cell biology Trachea Endocrinology Muscle relaxation Pertussis Toxin chemistry Enzyme Induction Phosphodiesterase 4 Inhibitors Rabbits Signal transduction Rolipram Muscle Contraction Signal Transduction |
| Zdroj: | American Journal of Physiology-Lung Cellular and Molecular Physiology. 294:L1055-L1067 |
| ISSN: | 1522-1504 1040-0605 |
| DOI: | 10.1152/ajplung.00021.2008 |
| Popis: | β2-Adrenergic receptor (β2AR) agonists acutely relieve bronchoconstriction via cAMP-mediated relaxation of airway smooth muscle (ASM). Airway constrictor responsiveness may be significantly heightened, however, following protracted exposure to these agents, presumably reflecting the effects of β2AR desensitization in ASM accompanying prolonged cAMP signaling. Because cAMP phosphodiesterase (PDE) activity can significantly modulate ASM contractility, we investigated the mechanism regulating PDE expression and its potential role in mediating changes in agonist-induced constrictor and relaxation responsiveness in ASM following its heterologous β2AR desensitization by prolonged exposure to cAMP-elevating agents. Isolated rabbit ASM tissues and cultured human ASM cells treated for 24 h with the receptor- or nonreceptor-coupled cAMP-stimulating agent, prostaglandin E2(PGE2) or forskolin, respectively, exhibited constrictor hyperresponsiveness to acetylcholine and impaired β2AR-mediated relaxation and cAMP accumulation. These proasthmatic-like changes in ASM function were associated with upregulated PDE4 activity, reflective of increased transcription of the PDE4D5 isoform, and were prevented by pretreatment of the ASM with a PDE4 inhibitor. Extended studies using gene silencing and pharmacological approaches to inhibit specific intracellular signaling molecules demonstrated that the mechanism underlying PGE2-induced transcriptional upregulation of PDE4D5 involves PKA-dependent activation of Giprotein signaling via the βγ-subunits, the latter eliciting downstream activation of ERK1/2 and its consequent induction of PDE4D5 transcription. Collectively, these findings identify that β2AR desensitization in ASM following prolonged exposure to cAMP-elevating agents is associated with proasthmatic-like changes in ASM responsiveness that are mediated by upregulated PDE4 expression induced by activated cross talk between the PKA and ERK1/2 signaling pathways. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|