Pregled bibliografske jedinice broj: 255587
Peptidoglycan monomer as a modulator of gp96 expression during liver regeneration in mice
Peptidoglycan monomer as a modulator of gp96 expression during liver regeneration in mice // Poster abstracts 2006 NIAID Research Conference / National Institutes of Health (ur.).
Bethesda (MD): US Department of Health and Human Services, 2006. str. 45-45. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 255587 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Peptidoglycan monomer as a modulator of gp96 expression during liver regeneration in mice
Autori
Radošević-Stašić, Biserka ; Mrakovčić-Šutić, Ines ; Jakovac, Hrvoje, Grebić, Damir ; Tomac, Jelena ; Rukavina, Daniel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Poster abstracts 2006 NIAID Research Conference
/ National Institutes of Health - Bethesda (MD) : US Department of Health and Human Services, 2006, 45-45.
Skup
2006 NIAID Research Conference
Mjesto i datum
Opatija, Hrvatska, 24.06.2006. - 30.06.2006
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
peptidoglycan monomer -Zn; partial hepatectomy; liver; thymus; spleen
Sažetak
In an attempt to analyze the possibility that damage-associated and pathogen-associated signals change the tissue expression of heat shock protein-gp96, which as molecular chaperone participates in correction of unfolded or misfolded proteins and acts as a natural adjuvant for chaperoning antigenic self peptides into the immune surveillance pathways, in this study, we analyzed its expression in: 1) partially hepatectomized mice (pHx), 2) in mice treated in vivo with peptidoglycan-monomer linked with zinc (PGM-Zn), and 3) in pHx mice treated with PGM-Zn. Gp96 proteins were determined by immunohistochemistry and the data were correlated with phenotype and cytotoxicity of hepatic and splenic mononuclear lymphatic cells (MNLC) against the NK sensitive (YAC-1) and NKT sensitive (syngeneic thymocytes) targets. It was found that each procedure markedly upregulated the gp96 expression in the liver and in the spleen, and that treatment of pHx mice with PGM-Zn additionally enhanced this expression. The later procedure increased also the proportion of NKT cells in the liver and the cytotoxicity of hepatic MNLC against YAC. In the spleen, however, PGM-Zn in combination with pHx increased only the early cytotoxicity against syngeneic thymocytes (24h after pHx), and decreased the cytotoxicity against YAC-target (24h and 48h after pHx). The data point to morphogenetic functions of gp96 during liver regeneration and suggest that PGM-Zn through Toll-like receptors or by Zn++ might affect the chaperone-mediated signaling.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
0062018
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Hrvoje Jakovac
(autor)
Damir Grebić
(autor)
Ines Mrakovčić-Šutić
(autor)
Biserka Radošević-Stašić
(autor)
Jelena Tomac
(autor)
Daniel Rukavina
(autor)