Pregled bibliografske jedinice broj: 882249
Open MHC-I conformers recycle via late endosomal recycling route
Open MHC-I conformers recycle via late endosomal recycling route // 3rd Meeting of Midle-European Societies for Immunology and Allergology ; Abstract book
Budimpešta, 2016. str. 92-92 (poster, nije recenziran, sažetak, ostalo)
CROSBI ID: 882249 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Open MHC-I conformers recycle via late endosomal recycling route
Autori
Mahmutefendić, Hana ; Blagojević Zagorac, Gordana ; Grabušić, Kristina ; Karleuša, Ljerka ; Mačešić, Senka ; Momburg, Frank ; Lučin, Pero
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Izvornik
3rd Meeting of Midle-European Societies for Immunology and Allergology ; Abstract book
/ - Budimpešta, 2016, 92-92
Skup
3rd Meeting of Midle-European Societies for Immunology and Allergology
Mjesto i datum
Budimpešta, Mađarska, 01.12.2017. - 03.12.2017
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
late endosomes, MHC-I, recycling
Sažetak
With an increasing number of endosomal cargo molecules studied, it is becoming clear that endocytic routes are diverse, and the cell uses more pathways to adjust expression of cell surface proteins. Intracellular itinerary of integral membrane proteins that avoid the early endosomal recycling route is not enough studied. Therefore, we studied endocytic trafficking of empty Ld (eLd) molecules, an open form of murine MHC-I allele, in fibroblast-like cells. Pulse labeling of cell surface eLd with mAbs and internalization kinetics suggest two steps of endosomal recycling: rapid and late. The same kinetics was also observed for human open MHC-I conformers. Kinetic modeling, using in-house developed software for multicompartment analysis, colocalization studies and established protocols for enriched labeling of the late endosomal (LE) pool of eLd demonstrated that the late step of recycling occurs from an LE compartment. Although the majority of eLd distributed into pre-degradative multivesicular bodies (MVBs), these LE subsets were not a source for eLd recycling. The LE recycling of eLd did not require Rab7 membrane domains, as demonstrated by Rab7-silencing, but required vectorial LE motility, suggesting that LE recycling occurs from dynamic tubulovesicular LE domains prior segregation of eLd in MVBs. Thus, our study indicates that LE system should not be simply considered as a feeder for loading of the degradative tract of the cell but also as a feeder for loading of the plasma membrane and thereby contribute to the maintenance of homeostasis of plasma membrane proteins.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
HRZZ IP-2014-09-9564
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Gordana Blagojević Zagorac
(autor)
Hana Mahmutefendić Lučin
(autor)
Ljerka Karleuša
(autor)
Pero Lučin
(autor)
Kristina Grabušić
(autor)