Pregled bibliografske jedinice broj: 310196
Regulation of granulysin protein expression in decidual NK cells by Th1 cytokines and antigen presenting cells
Regulation of granulysin protein expression in decidual NK cells by Th1 cytokines and antigen presenting cells // American Journal of Reproductive Immunology / Beaman, Kenneth ; Rukavina, Daniel (ur.).
Oxford: Wiley-Blackwell, 2007. str. 449-450 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 310196 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Regulation of granulysin protein expression in decidual NK cells by Th1 cytokines and antigen presenting cells
Autori
Veljkovic, Danijela ; Laskarin, Gordana ; Haller, Herman ; Saito, Sigeru ; Le Bouteiller, Philippe ; Rukavina, Daniel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
American Journal of Reproductive Immunology
/ Beaman, Kenneth ; Rukavina, Daniel - Oxford : Wiley-Blackwell, 2007, 449-450
Skup
X International Congress of Reproductive Immunology
Mjesto i datum
Opatija, Hrvatska, 10.06.2007. - 14.06.2007
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
pregnancy; granulysin; decidual NK cells; Th1 cytokines
Sažetak
Problem: The aim of our study was to analyze the expression of a cytolytic protein granulysin in decidual CD56 positive cells after the stimulation with Th1 cytokines and decidual antigen presenting cells. Methods of study: Decidual mononuclear cells (DMC) were obtained by enzymatic digestion of decidual tissue and density gradient centrifugation. CD56+ cells and subsequently CD83+ cells were purified from the suspension of a non-adherent DMC fraction using positive magnetic separation after 18-hour culture at 37°C. The immature CD1a+ and subsequently CD14+ cells were isolated from the adherent DMC fraction. Granulysin expression was analyzed using cell permeabilisation method, flow cytometry, immunohistochemistry and confocal microscopy. Results: Approximately 90% of decidual CD56+CD3- NK cells express granulysin in their cytoplasmatic granules near the cell membrane. This percentage did not significantly change after 18-hour culture of NK cells in DMC suspension, nor after CD56 positive magnetic separation. The addition of anti-PIBF monoclonal antibody in the suspension of freshly isolated DMC decreased the percentage of granulysin expressing CD56+CD3- cells after 18-hour culture. The culture of purified CD56+ cells in the medium only for 18 hours, decreased the percentage of granulysin in their cytoplasm. This decrease is prevented by stimulation with IL-15, IL-2, and IL-18 in a dose-dependent manner. The co-culture of purified CD56+ cells with immature CD1a+ dendritic cells or CD14+ macrophages also upregulated the percentage of granulysin expressing NK cells, whereas CD83+ cells had no effect. Conclusion: Decidual tissue specific environment, comprising PIBF, cytokines and antigen presenting cells, favorizes granulysin expression in CD56+ NK cells. The experiments are partially financed by Croatian Ministry of Science (Grants No. 0620402-0376 and 0379) and EMBIC project, European FP6, NoE, LSHM-CT-2004-512040.
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)
062-0620402-0379 - Imunološki mehanizmi u žena s patološkim trudnoćama (Haller, Herman, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Herman Haller
(autor)
Daniel Rukavina
(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