Myosin-Va restrains the trafficking of Na+/K+-ATPase-containing vesicles in alveolar epithelial cells

Author:

Lecuona Emilia1,Minin Alexander23,Trejo Humberto E.1,Chen Jiwang1,Comellas Alejandro P.1,Sun Haiying1,Grillo Doris4,Nekrasova Oxana E.1,Welch Lynn C.1,Szleifer Igal4,Gelfand Vladimir I.2,Sznajder Jacob I.1

Affiliation:

1. Division of Pulmonary and Critical Care Medicine, Department of Medicine, Northwestern University, Chicago, IL 60611, USA

2. Department of Cell and Molecular Biology, Northwestern University, Chicago, IL 60611, USA

3. Institute of Protein Research, Russian Academy of Sciences, Moscow 119988, Russia

4. Department of Biomedical Engineering, Northwestern University, Evanston, IL 60208, USA

Abstract

Stimulation of Na+/K+-ATPase activity in alveolar epithelial cells by cAMP involves its recruitment from intracellular compartments to the plasma membrane. Here, we studied the role of the actin molecular motor myosin-V in this process. We provide evidence that, in alveolar epithelial cells, cAMP promotes Na+/K+-ATPase recruitment to the plasma membrane by increasing the average speed of Na+/K+-ATPase-containing vesicles moving to the cell periphery. We found that three isoforms of myosin-V are expressed in alveolar epithelial cells; however, only myosin-Va and Vc colocalized with the Na+/K+-ATPase in intracellular membrane fractions. Overexpression of dominant-negative myosin-Va or knockdown with specific shRNA increased the average speed and distance traveled by the Na+/K+-ATPase-containing vesicles, as well as the Na+/K+-ATPase activity and protein abundance at the plasma membrane to similar levels as those observed with cAMP stimulation. These data show that myosin-Va has a role in restraining Na+/K+-ATPase-containing vesicles within intracellular pools and that this restrain is released after stimulation by cAMP allowing the recruitment of the Na+/K+-ATPase to the plasma membrane and thus increased activity.

Publisher

The Company of Biologists

Subject

Cell Biology

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