Cellular receptors, differentiation and endocytosis requirements are key factors for type I IFN response by human epithelial, conventional and plasmacytoid dendritic infected cells by measles virus

التفاصيل البيبلوغرافية
العنوان: Cellular receptors, differentiation and endocytosis requirements are key factors for type I IFN response by human epithelial, conventional and plasmacytoid dendritic infected cells by measles virus
المؤلفون: T. Fabian Wild, Hélène Valentin, Johan Druelle, Chantal Rabourdin-Combe, Florence Herschke, Denis Gerlier, Stéphane Schicklin, Olga Azocar, Sébastien Plumet, Chistine Delprat, Thomas Duhen
المصدر: Virus Research. 152:115-125
بيانات النشر: Elsevier BV, 2010.
سنة النشر: 2010
مصطلحات موضوعية: Cancer Research, Cell type, Receptors, Cell Surface, Membrane Cofactor Protein, Measles virus, Signaling Lymphocytic Activation Molecule Family Member 1, Antigens, CD, Interferon, Virology, medicine, Humans, Receptor, Cells, Cultured, Tropism, biology, RIG-I, Wild type, Cell Differentiation, Epithelial Cells, Dendritic Cells, TLR7, biology.organism_classification, Endocytosis, Viral Tropism, Infectious Diseases, Interferon Type I, Immunology, Receptors, Virus, Measles, medicine.drug
الوصف: While the antiviral response during measles virus (MeV) infection is documented, the contribution of the hosting cell type to the type I interferon (IFN-alpha/beta) response is still not clearly established. Here, we report that a signature heterogeneity of the IFN-alpha/beta response according to the cell type. The MeV tropism dictated by the expression of appropriate cellular receptor appeared to be crucial for epithelial cells. For conventional DCs (cDCs), the maturation state played a prominent role. In response to both wild type MeV isolates and laboratory/vaccine strains, immature cDCs produced higher levels of IFN-alpha than mature cDCs, despite the reduced expression levels of both CD46 and CD150 receptors by the former ones. While in epithelial cells and cDCs the MeV transcription was required to activate the IFN-alpha/beta response, plasmacytoid DCs (pDCs) rapidly produced large amounts of IFN-alpha mostly independently of the viral infection cycle. This argues for a significant contribution of pDCs in response to MeV infection and/or vaccination.
تدمد: 0168-1702
DOI: 10.1016/j.virusres.2010.06.013
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee1e2a1a9c1f7efa4d35824afa33fa1b
https://doi.org/10.1016/j.virusres.2010.06.013
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....ee1e2a1a9c1f7efa4d35824afa33fa1b
قاعدة البيانات: OpenAIRE
الوصف
تدمد:01681702
DOI:10.1016/j.virusres.2010.06.013