Pregled bibliografske jedinice broj: 542438
Expression and regulation of CD91 at the maternal fetal interface
Expression and regulation of CD91 at the maternal fetal interface // Book of abstracts / Rudolf Valenta (ur.).
Beč: Austrian Society for allergology and Immunology, 2010. str. 41-41 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 542438 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Expression and regulation of CD91 at the maternal fetal interface
(Expression and regulation of CD91 at the maternal fetal interface.)
Autori
Laškarin, Gordana ; Redžović, Arnela ; Vlastelić, Ivan ; Haller, Herman ; Rukavina, Daniel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of abstracts
/ Rudolf Valenta - Beč : Austrian Society for allergology and Immunology, 2010, 41-41
Skup
Annual Meeting of the Austrian Society for Allergology and Immunology in co-operation with the national Societies of Croatia, Czech Republic, Hngary, Slovakia and Slovennia
Mjesto i datum
Beč, Austrija, 03.12.2010. - 05.12.2010
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
antigen presenting cells; CD91; dendritic cells; heat shock protein 70; NK cells; T cells; pregnancy; progesterone induced blocking factor
Sažetak
Heat shock protein 70 (HSP 70) is present in glandular epithelial cells and could be released during tissue remodeling at the maternal fetal-fetal interface of the first trimester normal pregnancy. It becomes forceful immunogen in the extracellular space and might compromise pregnancy. The aim of this study was to investigate the presence, distribution and regulation of CD91 receptor for HSP70 with specific progesterone mediator Progesterone Induced Blocking Factor (PIBF) in early pregnancy decidua. CD91+ cells with long extensions were found by immunohistology in the decidual stroma around the glands. Flow cytometry revealed the distribution of CD91 on NK cells and antigen presenting CD14+ macrophages, CD1a+ immature and CD83+ mature dendritic cells. T cells and NKT cells were CD91 negative. PIBF on a dose dependent manner decreased CD91 expression on mature CD83+ cells and cytotoxic CD56 dim+ NK subset, whereas it could not affect the expression of CD91 on immature CD1a+ cells and regulatory CD56 bright+ NK subset. Further, HSP 70 bound on CD91 on CD1a+ cells on a dose dependent manner, but it did not affect significantly their phenotype (CD80, CD86, CD83 and HLA-DR expression). Down-regulation of CD91 expression on activated decidual innate immune cells with PIBF contributes to the initiation of the immune response in normal early pregnancy decidua.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke 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,
Klinički bolnički centar Rijeka
Profili:
Herman Haller
(autor)
Ivan Vlastelić
(autor)
Daniel Rukavina
(autor)
Arnela Redžović
(autor)
Gordana Laškarin
(autor)