Pregled bibliografske jedinice broj: 167229
NK cell activation through the NKG2D ligand mult-1 is selectively prevented by the glycoprotein encoded by mouse cytomegalovirus gene M145
NK cell activation through the NKG2D ligand mult-1 is selectively prevented by the glycoprotein encoded by mouse cytomegalovirus gene M145 // Knjiga sažetaka: Annual Meeting of the Croatian Immunological Society 2004. / Jonjić, Stipan ; Gagro, Alenka ; Polić, Bojan (ur.).
Rijeka, 2004. (poster, nije recenziran, sažetak, stručni)
CROSBI ID: 167229 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
NK cell activation through the NKG2D ligand mult-1 is selectively prevented by the glycoprotein encoded by mouse cytomegalovirus gene M145
Autori
Krmpotić, Astrid ; Hasan, Milena ; Loewendorf, Amdrea ; Saulig, Tanja ; Halenius, Anne ; Lenac, Tihana ; Polić, Bojan ; Bubić, Ivan ; Kriegeskorte, Anja ; Pernjak-Pugel, Ester ; Messerle, Martin ; Hengel, Hartmut ; Busch, Dirk H. ; Koszinowski, Urlich H. ; Jonjić, Stipan
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Knjiga sažetaka: Annual Meeting of the Croatian Immunological Society 2004.
/ Jonjić, Stipan ; Gagro, Alenka ; Polić, Bojan - Rijeka, 2004
Skup
Annual Meeting of the Croatian Immunological Society 2004.
Mjesto i datum
Opatija, Hrvatska, 08.10.2004. - 10.10.2004
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
NK Cell
Sažetak
Mouse 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 and found 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 glycoprotein encoded by m145 gene 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.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Astrid Krmpotić
(autor)
Ester Pernjak-Pugel
(autor)
Tanja Saulig
(autor)
Bojan Polić
(autor)
Milena Hasan
(autor)
Stipan Jonjić
(autor)
Ivan Bubić
(autor)
Tihana Lenac Roviš
(autor)