Adenosine regulation of alveolar fluid clearance

被引:63
作者
Factor, Phillip
Mutlu, Goskhan M.
Chen, Lan
Mohameed, Jameel
Akhmedov, Alexander T.
Meng, Fan Jing
Jilling, Tamas
Lewis, Erin Rachel
Johnson, Meshell D.
Xu, Anna
Kass, Daniel
Martino, Janice M.
Bellmeyer, Amy
Albazi, John S.
Emala, Charles
Lee, H. T.
Dobbs, Leland G.
Matalon, Sadis
机构
[1] Columbia Univ, New York, NY 10027 USA
[2] Northwestern Univ, Div Pulm & Crit Care Med, Chicago, IL 60611 USA
[3] Univ Alabama Birmingham, Dept Anesthesiol, Birmingham, AL 35294 USA
[4] Evanston NW Healthcare Res Inst, Evanston, IL 60201 USA
[5] Columbia Univ Coll Phys & Surg, Dept Anesthesiol, New York, NY 10032 USA
[6] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[7] NE Illinois Univ, Dept Chem, Chicago, IL 60625 USA
关键词
active sodium transport; adenosine receptors; cystic fibrosis; transmembrane conductance regulator;
D O I
10.1073/pnas.0601117104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Adenosine is a purine nucleoside that regulates cell function through G protein-coupled receptors that activate or inhibit adenylyl cyclase. Based on the understanding that cAMP regulates alveolar epithelial active Na+ transport, we hypothesized that adenosine and its receptors have the potential to regulate alveolar ion transport and airspace fluid content. Herein, we report that type 1 (A(1)R), 2a (A(2)aR), 2b(A(2b)R), and 3 (A(3)R) adenosine receptors are present in rat and mouse lungs and alveolar type 1 and 2 epithelial cells (AT1 and AT2). Rat AT2 cells generated and produced cAMP in response to adenosine, and micromolar concentrations of adenosine were measured in bronchoalveolar lavage fluid from mice. Ussing chamber studies of rat AT2 cells indicated that adenosine affects ion transport through engagement of A(1)R, A(2a)R, and/or A(3)R through a mechanism that increases CFTR and amiloride-sensitive channel function. Intratracheal instillation of low concentrations of adenosine (<= 10(-8)M) or either A(2a)R- or A(3)R-specific agonists increased alveolar fluid clearance (AFC), whereas physiologic concentrations of adenosine (>= 10(-6)M) reduced AFC in mice and rats via an A(1)R-dependent pathway. Instillation of a CFTR inhibitor (CFTRinh-172) attenuated adenosine-mediated down-regulation of AFC, suggesting that adenosine causes Cl- efflux by means of CFTR. These studies report a role for adenosine in regulation of alveolar ion transport and fluid clearance. These findings suggest that physiologic concentrations of adenosine allow the alveolar epithelium to counterbalance active Na+ absorption with Cl- efflux through engagement of the A(1)R and raise the possibility that adenosine receptor ligands can be used to treat pulmonary edema.
引用
收藏
页码:4083 / 4088
页数:6
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