Spatiotemporal changes of coxsackievirus and adenovirus receptor in rat hearts during postnatal development and in cultured cardiomyocytes of neonatal rat
T Kashimura, M Kodama, Y Hotta, J Hosoya, K Yoshida… - Virchows Archiv, 2004 - Springer
T Kashimura, M Kodama, Y Hotta, J Hosoya, K Yoshida, T Ozawa, R Watanabe, Y Okura…
Virchows Archiv, 2004•SpringerCoxsackievirus B is the most common cause of viral myocarditis and is particularly virulent in
neonates and children. Adenovirus is also a leading cause of the disease. The determinant
of tropism for both viruses is considered to be the expression of coxsackievirus and
adenovirus receptor (CAR) in target organs. However, developmental change and
physiological localization of CAR in the heart are unknown. We examined expression levels
of CAR in rat hearts by quantitative real-time polymerase chain reaction and Western blot …
neonates and children. Adenovirus is also a leading cause of the disease. The determinant
of tropism for both viruses is considered to be the expression of coxsackievirus and
adenovirus receptor (CAR) in target organs. However, developmental change and
physiological localization of CAR in the heart are unknown. We examined expression levels
of CAR in rat hearts by quantitative real-time polymerase chain reaction and Western blot …
Abstract
Coxsackievirus B is the most common cause of viral myocarditis and is particularly virulent in neonates and children. Adenovirus is also a leading cause of the disease. The determinant of tropism for both viruses is considered to be the expression of coxsackievirus and adenovirus receptor (CAR) in target organs. However, developmental change and physiological localization of CAR in the heart are unknown. We examined expression levels of CAR in rat hearts by quantitative real-time polymerase chain reaction and Western blot analysis and found that CAR decreased gradually during postnatal development, although CAR was detectable, even in adults. Immunohistochemistry revealed CAR on the whole surface of cardiomyocytes in immature rat hearts. In contrast, CAR was detected predominantly on intercalated disks in the adult heart and was accumulated especially at the contact point between the cultured cardiomyocytes, even though they were prepared from the neonatal rat heart. In conclusion, CAR was expressed abundantly on the whole surface of cardiomyocytes in immature rat hearts. Both the expression level and the localization of CAR are possible determinants of the susceptibility to viral myocarditis of neonates and children.
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