Division of Pulmonary, Critical Care, Sleep & Allergy, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE 68198-5910, USA.
Am J Physiol Lung Cell Mol Physiol. 2011 Aug;301(2):L171-80. doi: 10.1152/ajplung.00203.2010. Epub 2011 May 27.
Mucociliary clearance, vital to lung clearance, is dependent on cilia beat frequency (CBF), coordination of cilia, and the maintenance of periciliary fluid. Adenosine, the metabolic breakdown product of ATP, is an important modulator of ciliary motility. However, the contributions of specific adenosine receptors to key airway ciliary motility processes are unclear. We hypothesized that adenosine modulates ciliary motility via activation of its cell surface receptors (A(1), A(2A), A(2B), or A(3)). To test this hypothesis, mouse tracheal rings (MTRs) excised from wild-type and adenosine receptor knockout mice (A(1), A(2A), A(2B), or A(3), respectively), and bovine ciliated bronchial epithelial cells (BBECs) were stimulated with known cilia activators, isoproterenol (ISO; 10 μM) and/or procaterol (10 μM), in the presence or absence of 5'-(N-ethylcarboxamido) adenosine (NECA), a nonselective adenosine receptor agonist [100 nM (A(1), A(2A), A(3)); 10 μM (A(2B))], and CBF was measured. Cells and MTRs were also stimulated with NECA (100 nM or 10 μM) in the presence and absence of adenosine deaminase inhibitor, erythro-9- (2-hydroxy-3-nonyl) adenine hydrochloride (10 μM). Both ISO and procaterol stimulated CBF in untreated cells and/or MTRs from both wild-type and adenosine knockout mice by ~3 Hz. Likewise, CBF significantly increased ~2-3 Hz in BBECs and wild-type MTRs stimulated with NECA. MTRs from A(1), A(2A), and A(3) knockout mice stimulated with NECA also demonstrated an increase in CBF. However, NECA failed to stimulate CBF in MTRs from A(2B) knockout mice. To confirm the mechanism by which adenosine modulates CBF, protein kinase activity assays were conducted. The data revealed that NECA-stimulated CBF is mediated by the activation of cAMP-dependent PKA. Collectively, these data indicate that purinergic stimulation of CBF requires A(2B) adenosine receptor activation, likely via a PKA-dependent pathway.
黏液纤毛清除功能对于肺部清除至关重要,它依赖于纤毛的摆动频率(CBF)、纤毛的协调以及纤毛周围液体的维持。腺苷是三磷酸腺苷(ATP)代谢分解产物,是纤毛运动的重要调节剂。然而,特定的腺苷受体对关键气道纤毛运动过程的贡献尚不清楚。我们假设腺苷通过激活其细胞表面受体(A1、A2A、A2B 或 A3)来调节纤毛运动。为了验证这一假设,从野生型和腺苷受体敲除小鼠(分别为 A1、A2A、A2B 或 A3)中分离出气管环(MTRs)和牛纤毛支气管上皮细胞(BBECs),用已知的纤毛激活剂异丙肾上腺素(ISO;10 μM)和/或丙卡特罗(10 μM)刺激,同时存在或不存在 5'-(N-乙基羧酰胺)腺苷(NECA),一种非选择性腺苷受体激动剂[100 nM(A1、A2A、A3);10 μM(A2B)],并测量 CBF。细胞和 MTRs 也在用腺苷脱氨酶抑制剂,Erythro-9-(2-羟基-3-壬基)腺嘌呤盐酸盐(10 μM)处理的情况下用 NECA(100 nM 或 10 μM)刺激。ISO 和丙卡特罗均刺激未处理的细胞和/或来自野生型和腺苷敲除小鼠的 MTRs 的 CBF 增加约 3 Hz。同样,BBECs 和野生型 MTRs 用 NECA 刺激时,CBF 显著增加约 2-3 Hz。用 NECA 刺激 A1、A2A 和 A3 敲除小鼠的 MTRs 也显示 CBF 增加。然而,NECA 未能刺激 A2B 敲除小鼠的 MTRs 中的 CBF。为了确认腺苷调节 CBF 的机制,进行了蛋白激酶活性测定。数据显示,NECA 刺激的 CBF 是通过激活 cAMP 依赖性蛋白激酶 A(PKA)介导的。总的来说,这些数据表明嘌呤能刺激 CBF 需要 A2B 腺苷受体的激活,可能通过 PKA 依赖途径。