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NK Cell Activation Through the NKG2D Ligand MULT-1 is Selectively Prevented by the Glycoprotein Encoded by Mouse Cytomegalovirus Gene m145 (CROSBI ID 108878)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Krmpotić, Astrid ; Hasan, Milena ; Loewendorf, Andrea ; Saulig, Tanja ; Halenius, Anne ; Lenac, Tihana ; Polić, Bojan ; Bubić, Ivan ; Kriegeskorte, Anja ; Pernjak-Pugel, Ester et al. NK Cell Activation Through the NKG2D Ligand MULT-1 is Selectively Prevented by the Glycoprotein Encoded by Mouse Cytomegalovirus Gene m145 // The Journal of experimental medicine, 201 (2005), 2; 211-220-x

Podaci o odgovornosti

Krmpotić, Astrid ; Hasan, Milena ; Loewendorf, Andrea ; Saulig, Tanja ; Halenius, Anne ; Lenac, Tihana ; Polić, Bojan ; Bubić, Ivan ; Kriegeskorte, Anja ; Pernjak-Pugel, Ester ; Messerle, Martin ; Hengel, Hartmut ; Busch, Dirk ; Koszinowski, Ulrich ; Jonjić, Stipan

engleski

NK Cell Activation Through the NKG2D Ligand MULT-1 is Selectively Prevented by the Glycoprotein Encoded by Mouse Cytomegalovirus Gene m145

The NK cell activating receptor NKG2D interacts with three different cellular ligands, all of which are regulated by mouse cytomegalovirus (MCMV). We set out to define the viral gene product regulating MULT-1, a newly described NKG2D ligand. We show that MCMV infection strongly induces MULT-1 gene expression, but surface expression of this glycoprotein is nevertheless completely abolished by the virus. Screening a panel of MCMV deletion mutants defined the gene m145 as the viral regulator of MULT-1. The MCMV m145-encoded glycoprotein turned out to be necessary and sufficient to regulate MULT-1 by preventing plasma membrane residence of MULT-1. The importance of MULT-1 in NK cell regulation in vivo was confirmed by the attenuating effect of the m145 deletion which was lifted after NK cell depletion. Our findings underline the significance of escaping MULT-1/NKG2D signaling for viral survival and maintenance.

MCMV; m145 gene; MULT-1; NKG2D; immunoevasion

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Podaci o izdanju

201 (2)

2005.

211-220-x

objavljeno

0022-1007

Povezanost rada

Temeljne medicinske znanosti, Kliničke medicinske znanosti

Indeksiranost