Asunto(s)
Moléculas de Adhesión Celular/fisiología , Coronavirus Humano 229E/patogenicidad , Lectinas Tipo C/fisiología , Receptores de Superficie Celular/fisiología , Enzima Convertidora de Angiotensina 2 , Animales , Antígenos CD13/química , Células CHO , Moléculas de Adhesión Celular/química , Línea Celular , Cricetinae , Células Dendríticas/virología , Citometría de Flujo , Humanos , Lectinas Tipo C/química , Ratones , Peptidil-Dipeptidasa A/fisiología , Unión Proteica , Receptores de Superficie Celular/químicaRESUMEN
In several mammalian species, including humans, coronavirus infection can modulate the host immune response. We show a potential role of dendritic cells (DC) in murine coronavirus-induced immune modulation and pathogenesis by demonstrating that the JAW SII DC line and primary DC from BALB/c mice and p/p mice with reduced expression of the murine coronavirus receptor, murine CEACAM1a, are susceptible to murine coronavirus infection by a receptor-dependent pathway.
Asunto(s)
Células Dendríticas/virología , Glicoproteínas/fisiología , Virus de la Hepatitis Murina/patogenicidad , Receptores Virales/fisiología , Animales , Antígenos CD , Antígeno CD11c/análisis , Antígeno Carcinoembrionario , Moléculas de Adhesión Celular , Línea Celular , Células Cultivadas , Ratones , Ratones Endogámicos BALB C , Linfocitos T/inmunologíaRESUMEN
Truncated human coronavirus HCoV-229E spike glycoproteins containing amino acids 407 to 547 bound to purified, soluble virus receptor, human aminopeptidase N (hAPN). Soluble hAPN neutralized the infectivity of HCoV-229E virions at 37 degrees C, but not 4 degrees C. Binding of hAPN may therefore trigger conformational changes in the viral spike protein at 37 degrees C that facilitate virus entry.
Asunto(s)
Antígenos CD13/fisiología , Coronavirus Humano 229E/fisiología , Coronavirus Humano 229E/patogenicidad , Receptores Virales/fisiología , Secuencia de Aminoácidos , Animales , Sitios de Unión , Antígenos CD13/química , Antígenos CD13/genética , Línea Celular , Coronavirus Humano 229E/genética , Humanos , Glicoproteínas de Membrana/química , Glicoproteínas de Membrana/genética , Glicoproteínas de Membrana/fisiología , Unión Proteica , Conformación Proteica , Estructura Terciaria de Proteína , Receptores de Coronavirus , Receptores Virales/química , Receptores Virales/genética , Eliminación de Secuencia , Solubilidad , Glicoproteína de la Espiga del Coronavirus , Proteínas del Envoltorio Viral/química , Proteínas del Envoltorio Viral/genética , Proteínas del Envoltorio Viral/fisiologíaRESUMEN
Angiotensin-converting enzyme 2 (ACE2) is a receptor for SARS-CoV, the novel coronavirus that causes severe acute respiratory syndrome [Li, W. Moore, M. J., Vasilieva, N., Sui, J., Wong, S. K., Berne, M. A., Somasundaran, M., Sullivan, J. L., Luzuriaga, K., Greenough, T. C., et al. (2003) Nature 426, 450-454]. We have identified a different human cellular glycoprotein that can serve as an alternative receptor for SARS-CoV. A human lung cDNA library in vesicular stomatitis virus G pseudotyped retrovirus was transduced into Chinese hamster ovary cells, and the cells were sorted for binding of soluble SARS-CoV spike (S) glycoproteins, S(590) and S(1180). Clones of transduced cells that bound SARS-CoV S glycoprotein were inoculated with SARS-CoV, and increases in subgenomic viral RNA from 1-16 h or more were detected by multiplex RT-PCR in four cloned cell lines. Sequencing of the human lung cDNA inserts showed that each of the cloned cell lines contained cDNA that encoded human CD209L, a C-type lectin (also called L-SIGN). When the cDNA encoding CD209L from clone 2.27 was cloned and transfected into Chinese hamster ovary cells, the cells expressed human CD209L glycoprotein and became susceptible to infection with SARS-CoV. Immunohistochemistry showed that CD209L is expressed in human lung in type II alveolar cells and endothelial cells, both potential targets for SARS-CoV. Several other enveloped viruses including Ebola and Sindbis also use CD209L as a portal of entry, and HIV and hepatitis C virus can bind to CD209L on cell membranes but do not use it to mediate virus entry. Our data suggest that the large S glycoprotein of SARS-CoV may use both ACE2 and CD209L in virus infection and pathogenesis.