Pregled bibliografske jedinice broj: 952963
Human adenovirus type 26 uses αv integrin for infection of human epithelial cells
Human adenovirus type 26 uses αv integrin for infection of human epithelial cells // 43rd FEBS Congress, Biochemistry Forever, in FEBS Open Bio, Volume 8, Issue S1
Prag, Češka Republika, 2018. str. 201-201 doi:10.1002/2211-5463.12453 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 952963 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Human adenovirus type 26 uses αv integrin for infection of human epithelial cells
Autori
Nestić, Davor ; Uil, Taco ; Ma, Jiangtao ; Soumitra, Roy ; Velinga, Jort ; Baker, Andrew ; Custer, Jerome ; Majhen, Dragomira
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
43rd FEBS Congress, Biochemistry Forever, in FEBS Open Bio, Volume 8, Issue S1
/ - , 2018, 201-201
Skup
43rd FEBS Congress ''Biochemistry Forever''
Mjesto i datum
Prag, Češka Republika, 07.07.2018. - 12.07.2018
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
adenovirus ; receptor ; endocitoza ; integrin
Sažetak
Human adenovirus vectors based on type 5 (HAdV5) are the most commonly investigated adenoviral vectors for gene therapy and vaccination. Due to activation of the host innate immune responses as well as preexisting immunity to AdV5 wild type development of new strategies to evade undesired anti vector host immune responses is needed. One approach is the search for other types of adenoviruses that occur at low prevalence in human populations, such as human adenovirus type 26 (HAdV26). HAdV26 belongs to subgroup D and its natural tropism is still unknown. While HAdV26 immunogenicity in vivo is rather well described, basic biology of this virus, like receptor usage, is less well studied and defined. Hence, the main objective of this study was to investigate transduction efficacy and cell entry of HAdV26 in epithelial cells. As a cell model we used A549 and SK-OV-3 cells which have different expression of known adenovirus receptors: CAR, CD46 and αv integrin. We showed that HAdV26 transduces SK- OV-3 cells 4 times better than A549 indicating that SK-OV-3 cells might express molecule/s that HAdV26 uses as a receptor. Thus, we downregulated CAR, CD46 and αv integrin in A549 and SK-OV-3 cells and subsequently measured transduction efficacy and binding of HAdV26. Downregulation of αv integrin significantly decreased transduction efficacy and binding of HAdV26 in both A549 and SK-OV-3 cells. We obtained the same effect by measuring transduction efficacy of HAdV26 after antibody- mediated blocking of αv integrin Namely, blocking αv integrin in A549 cells efficiently decreased transduction efficacy of HAdV26. These results were further confirmed in A549 cells with increased expression of αv integrin. We stably transfected A549 cells with αv integrin expression plasmid and showed that overexpression of αv integrin increases binding and transduction efficacy of HAdV26 in A549 cells. Based on our results we conclude that HAdV26 uses αv integrin for infection of epithelial cells.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA
Projekti:
UIP-2014-09-3912 - Razumijevanje puta ulaska Adenovirusa tipa 26 u stanicu: način poboljšanja vektora za vakcinaciju (AdVEntPathVac) (Majhen, Dragomira, HRZZ - 2014-09) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Conference Proceedings Citation Index - Science (CPCI-S)
- Scopus