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Vitenshtein, A.* ; Weisblum, Y.* ; Hauka, S.* ; Halenius, A.* ; Oiknine-Djian, E.* ; Tsukerman, P.* ; Bauman, Y.* ; Bar-On, Y.* ; Stern-Ginossar, N.* ; Enk, J.* ; Ortenberg, R.* ; Tai, J.* ; Markel, G.* ; Blumberg, R.S.* ; Hengel, H.* ; Jonjic, S.* ; Wolf, D.G.* ; Adler, H. ; Kammerer, R.* ; Mandelboim, O.*

CEACAM1-mediated inhibition of virus production.

Cell Rep. 15, 2331-2339 (2016)
Verlagsversion DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
Cells in our body can induce hundreds of antiviral genes following virus sensing, many of which remain largely uncharacterized. CEACAM1 has been previously shown to be induced by various innate systems; however, the reason for such tight integration to innate sensing systems was not apparent. Here, we show that CEACAM1 is induced following detection of HCMV and influenza viruses by their respective DNA and RNA innate sensors, IFI16 and RIG-I. This induction is mediated by IRF3, which bound to an ISRE element present in the human, but not mouse, CEACAM1 promoter. Furthermore, we demonstrate that, upon induction, CEACAM1 suppresses both HCMV and influenza viruses in an SHP2-dependent process and achieves this broad antiviral efficacy by suppressing mTOR-mediated protein biosynthesis. Finally, we show that CEACAM1 also inhibits viral spread in ex vivo human decidua organ culture.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Transcription Factor; Protein; Interferon; Ceacam1; Induction; Adhesion; Innate; Shp-2; Immunity; Antigen
Sprache englisch
Veröffentlichungsjahr 2016
HGF-Berichtsjahr 2016
ISSN (print) / ISBN 2211-1247
e-ISSN 2211-1247
Zeitschrift Cell Reports
Quellenangaben Band: 15, Heft: 11, Seiten: 2331-2339 Artikelnummer: , Supplement: ,
Verlag Cell Press
Verlagsort Cambridge
Begutachtungsstatus Peer reviewed
Institut(e) Research Unit Gene Vector (AGV)
POF Topic(s) 30203 - Molecular Targets and Therapies
Forschungsfeld(er) Immune Response and Infection
PSP-Element(e) G-501500-006
PubMed ID 27264178
DOI 10.1016/j.celrep.2016.05.036
WOS ID WOS:000377776400003
Scopus ID 84974698225
Erfassungsdatum 2016-06-08
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