Adenovirus stimulates choline efflux by increasing expression of organic cation transporter-2

Am J Physiol Lung Cell Mol Physiol. 2005 Jan;288(1):L93-102. doi: 10.1152/ajplung.00184.2004. Epub 2004 Sep 17.

Abstract

We examined the effect of wild-type human adenovirus (Ad5) on choline transport in murine lung epithelia (MLE) and in rodent primary alveolar type II cells. Cells were active in pH-sensitive, reversible transport of choline, a process blocked pharmacologically with phenoxybenzamine, an inhibitor of organic cation transporters (OCT). PCR products for the choline transporters, OCT-1 and OCT-2, were detected, but only OCT-2 protein was robustly expressed within MLE and primary alveolar epithelial cells. Ad5 produced a two- to threefold increase in choline efflux from cells, resulting in a significant reduction in intracellular choline content and its major product, phosphatidylcholine. Effects of Ad5 on choline efflux were inhibited with phenoxybenzamine, and choline efflux was attenuated by OCT-2 small interfering RNA. Adenovirus also produced a dose-dependent increase in immunoreactive OCT-2 levels concomitant with increased cellular OCT-2 steady-state mRNA. These results indicate that adenoviruses can significantly disrupt choline trafficking in lung epithelia by upregulating expression of an alveolar protein involved in organic cation transport.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenoviridae / physiology*
  • Adenoviridae Infections / metabolism
  • Adenoviridae Infections / pathology
  • Animals
  • Biological Availability
  • Biological Transport
  • Cell Line
  • Choline / metabolism*
  • Choline / pharmacokinetics
  • Epithelial Cells / metabolism
  • Gene Expression
  • Lung / metabolism*
  • Lung / pathology
  • Lung / virology*
  • Mice
  • Mice, Inbred C57BL
  • Organic Cation Transport Proteins / antagonists & inhibitors
  • Organic Cation Transport Proteins / genetics
  • Organic Cation Transport Proteins / metabolism*
  • Organic Cation Transporter 2
  • Phenoxybenzamine / pharmacology
  • Phosphatidylcholines / metabolism
  • Pulmonary Alveoli / metabolism
  • Pulmonary Alveoli / pathology
  • Pulmonary Alveoli / virology
  • Rats
  • Up-Regulation

Substances

  • Organic Cation Transport Proteins
  • Organic Cation Transporter 2
  • Phosphatidylcholines
  • Slc22a2 protein, mouse
  • Slc22a2 protein, rat
  • lecithins, disaturated
  • Phenoxybenzamine
  • Choline