Abstract
The coxsackievirus and adenovirus receptor (CAR) is an essential cellular protein that is involved in cell adhesion, cell signaling, and viral infection. The 8-exon encoded isoform (CAR(Ex8)) resides at the apical surface of polarized epithelia, where it is accessible as a receptor for adenovirus entering the airway lumen. Given its pivotal role in viral infection, it is a target for antiviral strategies. To understand the regulation of CAR(Ex8) and determine the feasibility of receptor downregulation, the half-life of total and apical localized CAR(Ex8) was determined and correlated with adenovirus transduction. Total and apical CAR(Ex8) has a relatively short half-life of approximately 2 h. The half-life of apical CAR(Ex8) correlates well with adenovirus transduction. These results suggest that antiviral strategies that aim to degrade the primary receptor for apical adenovirus infection will be effective within a relatively short time frame after application.