4.6 Review

Targeting G protein-coupled receptor signaling in asthma

Journal

CELLULAR SIGNALLING
Volume 18, Issue 12, Pages 2105-2120

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2006.04.008

Keywords

G protein-coupled receptor; asthma; airway; airway smooth muscle; allergy; atopy; inflammation; beta-agonist; desensitization; contraction; relaxation; synthetic function; airway remodeling; beta-adrenergic receptor; proliferation; G protein; phospholipase C; adenylyl cyclase; calcium; bronchoconstriction; steroid; polymorphism

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Funding

  1. NHLBI NIH HHS [HL58506] Funding Source: Medline
  2. NIAID NIH HHS [AI05977] Funding Source: Medline

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The complex disease asthma, an obstructive lung disease in which excessive airway smooth muscle (ASM) contraction as well as increased ASM mass reduces airway lumen size and limits airflow, can be viewed as a consequence of aberrant airway G protein-coupled receptor (GPCR) function. The central role of GPCRs in determining airway resistance is underscored by the fact that almost every drug used in the treatment of asthma directly or indirectly targets either GPCR-ligand interaction, GPCR signaling, or processes that produce GPCR agonists. Although many airway cells contribute to the regulation of airway resistance and architecture, ASM properties and functions have the greatest impact on airway homeostasis. The theme of this review is that GPCR-mediated regulation of ASM tone and ASM growth is a major determinant of the acute and chronic features of asthma, and multiple strategies targeting GPCR signaling may be employed to prevent or manage these features. (c) 2006 Elsevier Inc. All rights reserved.

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