Pregled bibliografske jedinice broj: 310309
Decidual CD1a+ cells are able to shape the percentage and functions of CD56+bright and CD3+ cells at the maternal-fetal interface
Decidual CD1a+ cells are able to shape the percentage and functions of CD56+bright and CD3+ cells at the maternal-fetal interface // American Journal of Reproductive Immunology / Beaman, Kenneth (ur.).
Oxford: Wiley-Blackwell, 2007. str. 234-235 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 310309 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Decidual CD1a+ cells are able to shape the percentage and functions of CD56+bright and CD3+ cells at the maternal-fetal interface
Autori
Laškarin, Gordana ; Redžović, Arnela ; Rubeša, Željka ; Veljković, Danijela ; Vlastelić, Ivan ; Allavena, Paola ; Mantovani, Alberto ; Rukavina, Daniel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
American Journal of Reproductive Immunology
/ Beaman, Kenneth - Oxford : Wiley-Blackwell, 2007, 234-235
Skup
5th European Congress of Reproductive Immunology
Mjesto i datum
Berlin, Njemačka, 30.08.2007. - 02.09.2007
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
decidual mononuclear cells; decidua; pregnancy
Sažetak
Problem: Characteristics of decidual CD1a+ cells and their functional interactions with decidual lymphocyte subpopulations were investigated. Material and methods: The first trimester normal human pregnancy decidua was used for immunohistochemistry and the isolation of decidual mononuclear cells (DMC) by enzimatic digestion and gradient density centrifugation. Surface markers, intracellular cytokine and cytolytic mediators' expression in CD1a+ cells were analysed by multicolour flow cytometry. Decidual CD1a+ cells were isolated from the adherent, whereas CD56+ and CD3+ cells from the non-adherent DMC fraction by magnetic separation. They were co-cultured at different CD1a/NKcell and CD1a/T cell ratios, respectively. The proliferation, cytokines', cytolityc mediators' and NK cell receptors' expression were analyzed in CD56+ bright, as well as cytokine production in decidual T cells after the stimulation with CD1a+ cells. The cytotoxicity of CD1a+ cells against decidual T cells was tested using PKH-26 (red) cytotoxicity assay. Results: Decidua is abundant with CD1a+ cells that are mostly of myeloid origin with relatively low CD83, CD80, CD86 and CD56+ expression, but high HLA class I, HLA-DR and CD14 molecule expression. CD1a+ cells from freshly isolated suspensions express cytoloytic mediators and IL-15, IL-18, IFN- + and TNF- cytokines in the cytoplasm. CD1a+ cells enhance short and long term cytolytic mediators expression (18 hrs) and proliferation rate of NK cells (48 hrs), but decrease their pro-inflammatory (IL-15, IFN- TNF-α ) cytokines production and NKp46 receptor expression (18 hrs). Decidual CD1a+ cells by themselves neither affect IL- 4, nor IFN-g production in decidual T cells at DC/T cell ratio 1:5 after 3 days co-culture in vitro and kill CD3+ cells on a dose dependent manner. Conclusion: It seems that CD1a+ cells are able to shape the percentage and functions of CD56+bright and CD3+ cells 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 Grants No. 0620402-0376 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)
Daniel Rukavina
(autor)
Arnela Redžović
(autor)
Danijela Veljković Vujaklija
(autor)
Gordana Laškarin
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE