Pregled bibliografske jedinice broj: 310269
Mutual dendritic cell/NK interaction leads to their well balanced co-existence at the maternal-fetal interface
Mutual dendritic cell/NK interaction leads to their well balanced co-existence at the maternal-fetal interface // Book of Abstracts / Rabatić, Sabina (ur.).
Zagreb: Hrvatsko imunološko društvo, 2007. str. 12-12 (predavanje, domaća recenzija, sažetak, znanstveni)
CROSBI ID: 310269 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Mutual dendritic cell/NK interaction leads to their well balanced co-existence at the maternal-fetal interface
Autori
Laškarin, Gordana ; Redžović, Arnela ; Rubeša, Željka ; Vlastelić, Ivan ; Allavena, Paola ; Mantovani, Alberto ; Rukavina, Daniel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstracts
/ Rabatić, Sabina - Zagreb : Hrvatsko imunološko društvo, 2007, 12-12
Skup
2007 Annual Meeting of the Croatian Immunological Society
Mjesto i datum
Rovinj, Hrvatska, 19.10.2007. - 21.10.2007
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Domaća recenzija
Ključne riječi
dendritic cells; human pregnancy; decidua
Sažetak
Dendritic cell/NK (DC/NK) inter-reactions of the early human pregnancy deciduas were analyzed in vitro. The characterization of CD1a+ and CD83+ cells was performed in the suspension of freshly isolated decidual mononuclear cells (DMC) in terms of phenotype and intracellular cytokine detection. Intermediate HLA-DR expression, low co-stimulatory (CD80, CD86) and significant endocytic molecule expression with the presence of CCR5 chemokine receptor, CD14 and CD56 indicated immature phenotype of CD1a+ cells. CD83+ subpopulation showed more mature phenotype and lower percentage of IL-15 and IFN-gamma producing cells then CD1a+ cells. The magnetic separation of CD56+ and CD83+ cells from the non-adherent and CD1a+ from the adherent DMC fraction was established. Purified CD56+ cells were cultured in the medium only or co-cultured with enriched CD1a+ or CD83+ cells. The proliferation, NK cell receptors, intracellular cytokines and cytolytic mediators expression in CD56+ bright cells have been analyzed. Immature CD1a+ cells increased perforin, FasL and TRAIL expression in NK cells, but decreased NKp46 receptor expression and pro-inflammatory cytokine production (18 hours). CD83+ cells did not show such effects. CD1a+ cells caused higher proliferation rate of decidual CD56+ bright cells, then CD83+ cells. Both dendritic subpopulations can be killed by decidual CD56+ cells, measured by 2 hrs PKH-26 (red) cytotoxicity assay. It seems that mutual DC/NK interaction leads to their well balanced co-existence at the maternal-fetal interface. Acknowledgement: The experiments were financed by the grants of EMBIC European FP6 project No. 512040, LSHM-CT-2004-512040 and Croatian Ministry of Science, Education and Sports No. 0376 and No. 0377.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
062-0620402-0376 - Citokini i citolitički mehanizmi tijekom rane trudnoće (Rukavina, Daniel, MZOS ) ( CroRIS)
062-0620402-0377 - Imunoregulacijske funkcije antigen predočnih stanica tijekom rane trudnoće (Laškarin, Gordana, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Željka Rubeša
(autor)
Ivan Vlastelić
(autor)
Arnela Redžović
(autor)
Daniel Rukavina
(autor)
Gordana Laškarin
(autor)