Isoform-specific regulation and localization of the coxsackie and adenovirus receptor in human airway epithelia

• Published in: PloS one Vol. 5; no. 3; p. e9909
• Main Authors: Excoffon, Katherine J D A, Gansemer, Nicholas D, Mobily, Matthew E, Karp, Philip H, Parekh, Kalpaj R, Zabner, Joseph
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 26.03.2010; Public Library of Science (PLoS)
• Subjects: Adenoviridae Infections - metabolism; Adenoviruses; Amino acids; Animals; Bronchi - metabolism; Cell adhesion; Cell adhesion molecules; Cell culture; Cell Differentiation; Cell Membrane - metabolism; Cercopithecus aethiops; CHO Cells; Cloning; COS Cells; Coxsackie and Adenovirus Receptor-Like Membrane Protein; Cricetinae; Cricetulus; Cystic fibrosis; Egress; Epithelium - metabolism; Gene Expression Regulation; Genes; Genomes; Health aspects; Humans; Infection; Infections; Infectious Diseases/Respiratory Infections; Internal medicine; Isoforms; Localization; Medicine; Mice; Molecular Biology; Postsynaptic density proteins; Protein expression; Protein Isoforms; Protein Structure, Tertiary; Proteins; Receptors, Virus - biosynthesis; Receptors, Virus - genetics; Regulation; Respiratory Medicine/Respiratory Infections; Respiratory tract; RNA, Messenger - metabolism; Rodents; Serotypes; Signal transduction; Tight junctions; Trachea - metabolism; Viral infections; United States > US; Iowa City Iowa
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0009909

Adenovirus is an important respiratory pathogen. Adenovirus fiber from most serotypes co-opts the Coxsackie-Adenovirus Receptor (CAR) to bind and enter cells. However, CAR is a cell adhesion molecule localized on the basolateral membrane of polarized epithelia. Separation from the lumen of the airways by tight junctions renders airway epithelia resistant to inhaled adenovirus infection. Although a role for CAR in viral spread and egress has been established, the mechanism of initial respiratory infection remains controversial. CAR exists in several protein isoforms including two transmembrane isoforms that differ only at the carboxy-terminus (CAR(Ex7) and CAR(Ex8)). We found low-level expression of the CAR(Ex8) isoform in well-differentiated human airway epithelia. Surprisingly, in contrast to CAR(Ex7), CAR(Ex8) localizes to the apical membrane of epithelia where it augments adenovirus infection. Interestingly, despite sharing a similar class of PDZ-binding domain with CAR(Ex7), CAR(Ex8) differentially interacts with PICK1, PSD-95, and MAGI-1b. MAGI-1b appears to stoichiometrically regulate the degradation of CAR(Ex8) providing a potential mechanism for the apical localization of CAR(Ex8) in airway epithelial. In summary, apical localization of CAR(Ex8) may be responsible for initiation of respiratory adenoviral infections and this localization appears to be regulated by interactions with PDZ-domain containing proteins.