Tissue-Specific Deletion of the Coxsackievirus and Adenovirus Receptor Protects Mice from Virus-induced Pancreatitis and Myocarditis

被引:53
作者
Kallewaard, Nicole L. [1 ]
Zhang, Lili [1 ]
Chen, Jin-Wen [1 ]
Guttenberg, Marta [2 ,4 ]
Sanchez, Melissa D. [5 ]
Bergelson, Jeffrey M. [1 ,3 ]
机构
[1] Childrens Hosp Philadelphia, Div Infect Dis, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Dept Pathol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Pediat, Philadelphia, PA 19104 USA
[4] Univ Penn, Sch Med, Dept Pathol, Philadelphia, PA 19104 USA
[5] Univ Penn, Sch Vet Med, Dept Toxicol & Pathol, Philadelphia, PA 19104 USA
关键词
VIRAL MYOCARDITIS; IN-VIVO; INFECTION; EXPRESSION; PATHOGENESIS; HEXON; CELLS; MODEL; CROSS; ENTRY;
D O I
10.1016/j.chom.2009.05.018
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In cultured cells, infection by group B coxsackievirus (CVB) is mediated by the coxsackievirus and adenovirus receptor (CAR), but the importance of this molecule in CVB-induced disease has not been determined. We generated mice with tissue-specific ablation of CAR within each of two major CVB target organs, the pancreas and heart. In the pancreas, deletion of CAR resulted in a significant reduction in both virus titers and virus-induced tissue damage. Similarly, cardiomyocyte-specific CAR deletion resulted in a marked reduction in virus titer, infection-associated cytokine production, and histopathology within the heart. Consistent with the in vivo phenotype, CAR-deficient cardiomyocytes resisted infection in vitro. These results demonstrate a critical function for CAR in the pathogenesis of CVB infection in vivo and in virus tropism for the heart and pancreas.
引用
收藏
页码:91 / 98
页数:8
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