4.6 Review

Targeting G protein-coupled receptor signaling in asthma

期刊

CELLULAR SIGNALLING
卷 18, 期 12, 页码 2105-2120

出版社

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

关键词

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

资金

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

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据