Pregled bibliografske jedinice broj: 168136
FasL molecule is up-regulated in the epidermis of psoriatic lesion
FasL molecule is up-regulated in the epidermis of psoriatic lesion // 6th Alpe Adria Symposium on Psoriasis / Trevisan, Guido (ur.).
Trst: University of Trieste, 2003. str. 5-5 (predavanje, međunarodna recenzija, sažetak, znanstveni)
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Naslov
FasL molecule is up-regulated in the epidermis of psoriatic lesion
Autori
Kaštelan, Marija ; Prpić Massari, Larisa ; Zamolo, Gordana ; Zauhar, G ; Gruber, Franjo ; Rukavina, Danijel
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
6th Alpe Adria Symposium on Psoriasis
/ Trevisan, Guido - Trst : University of Trieste, 2003, 5-5
Skup
6th Alpe Adria Symposium on Psoriasis
Mjesto i datum
Venecija, Italija; Bibione, Italija, 07.11.2003. - 08.11.2003
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
FasL; psoriasis
Sažetak
The role of cell-mediated cytotoxicity in psoriasis is not yet understood. Cytotoxic CD8+ T cells mediate cytotoxic reactions mainly by two different pathways, perforin/granzyme and Fas/FasL pathway while CD4+ T cells preferientialy use Fas/FasL system. In the present study we analyzed asL expression in both, epidermis and dermis, of lesional psoriatic skin (n=9), non-lesional psoriatic skin (n=9) and healthy constrol (n=8) by immunohistochemistry using biotin-streptavidin-peroxidase method. In epidermis, we found a significant increase in CD4+ and CD8+ T cells in lesions compared with non-lesional and helathy epidermis. The expression of FasL was also significantly higher in the lesional compared with non-lesional espidermis. In addtion, FasL expression was almost two times higher in epidermis than in dermis of psoriatic lesions. In conclusion, our results clearly point out the potential role of FasL cytolytic pathway in the development of psoriatic plaque.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti