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Absence of muscarinic cholinergic airway responses in mice deficient in the cyclic nucleotide phosphodiesterase PDE4D

机译:缺乏环核苷酸磷酸二酯酶PDE4D的小鼠中没有毒蕈碱胆碱能气道反应

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摘要

Muscarinic cholinergic signaling plays an essential role in the control of the normal airway functions and in the development of pulmonary pathologies including asthma. In this paper we demonstrate that the airways of mice deficient in a cAMP-specific phosphodiesterase (PDE4D) are no longer responsive to cholinergic stimulation. Airway hyperreactivity that follows exposure to antigen was also abolished in PDE4D−/− mice, despite an apparently normal lung inflammatory infiltration. The loss of cholinergic responsiveness was specific to the airway, not observed in the heart, and was associated with a loss of signaling through muscarinic receptors with an inability to decrease cAMP accumulation. These findings demonstrate that the PDE4D gene plays an essential role in cAMP homeostasis and cholinergic stimulation of the airway, and in the development of hyperreactivity. In view of the therapeutic potentials of PDE4 inhibitors, our findings provide the rationale for novel strategies that target a single PDE isoenzyme.
机译:毒蕈碱胆碱能信号在控制正常气道功能以及在包括哮喘在内的肺部疾病的发展中起着至关重要的作用。在本文中,我们证明了缺乏cAMP特异性磷酸二酯酶(PDE4D)的小鼠的气道不再对胆碱能刺激有反应。尽管显然肺炎性浸润正常,但在PDE4D -/-小鼠中也消除了抗原暴露后的气道高反应性。胆碱能反应性的丧失是特定于气道的,在心脏中未观察到,并且与毒蕈碱受体的信号传导丧失有关,无法降低cAMP的积累。这些发现表明,PDE4D基因在cAMP稳态和气道胆碱能刺激以及高反应性发展中起重要作用。考虑到PDE4抑制剂的治疗潜力,我们的发现为针对单一PDE同工酶的新策略提供了理论依据。

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