Pregled bibliografske jedinice broj: 395760
Differential susceptibility of RAE-1 isoforms to murine cytomegalovirus
Differential susceptibility of RAE-1 isoforms to murine cytomegalovirus // NK2008 11th Meeting of the Society for Natural Immunity, Fremantle, Western Australia, 26th - 30th October 2008 / Adoniou C. , Coudert (ur.).
Fremantle, 2008. str. 40-40 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 395760 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Differential susceptibility of RAE-1 isoforms to murine cytomegalovirus
Autori
Arapović, Jurica ; Lenac, Tihana ; Antulov, Ronald ; Polić, Bojan ; Carayannopoulos, L.N. ; Krmpotić, Astrid ; Jonjić, Stipan
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
NK2008 11th Meeting of the Society for Natural Immunity, Fremantle, Western Australia, 26th - 30th October 2008
/ Adoniou C. , Coudert - Fremantle, 2008, 40-40
Skup
NK2008 11th Meeting of the Society for Natural Immunity, Fremantle, Western Australia, 26th - 30th October 2008
Mjesto i datum
Fremantle, Australija, 26.10.2008. - 30.10.2008
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
MCMV; NKG2D; RAE-1; immunoevasion
Sažetak
NKG2D receptor is one of the most potent activating NK cell receptors involved in antiviral responses. NKG2D ligands in mouse are MULT-1, H60 and RAE-1 family of proteins. We and others have characterized several murine cytomegalovirus (MCMV) proteins involved in the down-modulation of NKG2D ligands. Among these, the gp40 encoded by m152 gene, originally described for its ability to block the maturation of MHC I molecules was also involved in down-modulation of RAE-1 proteins. Based on our initial observations suggesting that in some mouse strains the NKG2D-dependent control is preserved even in response to wild type MCMV, we postulated that there must be NKG2D ligands that resist the virus mediated down-modulation. Here we show that the RAE-1 proteins differ in their susceptibility to the down-regulation by MCMV due to intrinsic differences in stability of the mature surface-expressed protein. In contrast to RAE-1gamma, representing the sensitive isoform, RAE-1delta remains present on the surface of MCMV-infected cells. However, although unable to affect the mature RAE-1delta form, m152 retains the newly synthesized RAE-1delta as well as RAE-1gamma in the endoplasmic reticulum. The different stabilities of RAE-1 isoforms during MCMV infection can be attributed to the absence of the PLWY motif from RAE-1delta.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
062-0621261-1263 - Molekularni mehanizmi citomegalovirusnog izmicanja imunološkom nadzoru (Jonjić, Stipan, MZOS ) ( CroRIS)
062-0621261-1268 - Uloga imunosubverzivnih citomegalovirusnih gena u latenciji (Krmpotić, Astrid, MZOS ) ( CroRIS)
062-0621261-1271 - Uloga NKG2D u razvoju, homeostazi i efektorskim funkcijama imunološkog sustava (Polić, Bojan, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Jurica Arapović
(autor)
Astrid Krmpotić
(autor)
Stipan Jonjić
(autor)
Bojan Polić
(autor)
Tihana Lenac Roviš
(autor)
Ronald Antulov
(autor)