The tight junction protein CAR regulates cardiac conduction and cell–cell communication

Author:

Lisewski Ulrike1,Shi Yu1,Wrackmeyer Uta1,Fischer Robert2,Chen Chen1,Schirdewan Alexander23,Jüttner Rene4,Rathjen Fritz4,Poller Wolfgang3,Radke Michael H.1,Gotthardt Michael15

Affiliation:

1. Neuromuscular and Cardiovascular Cell Biology

2. HELIOS Kliniken GmbH, Franz-Volhard Klinik, Charité, Humboldt University, 13125 Berlin, Germany

3. Department of Cardiology, Campus Benjamin Franklin, D-12200 Berlin, Germany

4. Developmental Neurobiology, Max Delbrück Center for Molecular Medicine (MDC), 13122 Berlin-Buch, Germany

5. Department of Veterinary and Comparative Anatomy, Pharmacology, and Physiology, Washington State University, Pullman, WA 99164

Abstract

The Coxsackievirus-adenovirus receptor (CAR) is known for its role in virus uptake and as a protein of the tight junction. It is predominantly expressed in the developing brain and heart and reinduced upon cardiac remodeling in heart disease. So far, the physiological functions of CAR in the adult heart are largely unknown. We have generated a heart-specific inducible CAR knockout (KO) and found impaired electrical conduction between atrium and ventricle that increased with progressive loss of CAR. The underlying mechanism relates to the cross talk of tight and gap junctions with altered expression and localization of connexins that affect communication between CAR KO cardiomyocytes. Our results indicate that CAR is not only relevant for virus uptake and cardiac remodeling but also has a previously unknown function in the propagation of excitation from the atrium to the ventricle that could explain the association of arrhythmia and Coxsackievirus infection of the heart.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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