Pregled bibliografske jedinice broj: 83172
4-hydroxynonenal and splenic cells modify in vitro growth of rat hepatocytes
4-hydroxynonenal and splenic cells modify in vitro growth of rat hepatocytes // First International Meeting of the HNE-Club: 4-hydroxynonenal and other lipid peroxidation products : Book of abstracts
Salzburg, 2002. str. 51-51 (poster, međunarodna recenzija, sažetak, znanstveni)
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Naslov
4-hydroxynonenal and splenic cells modify in vitro growth of rat hepatocytes
Autori
Čipak, Ana ; Brasgen, Nikolaus ; Šćukanec, Mira ; Kirac, Iva ; Eckl, Peter ; Žarković, Neven
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
First International Meeting of the HNE-Club: 4-hydroxynonenal and other lipid peroxidation products : Book of abstracts
/ - Salzburg, 2002, 51-51
Skup
International Meeting of the HNE-Club: 4-hydroxynonenal and other lipid peroxidation products (1 ; 2002)
Mjesto i datum
Salzburg, Austrija, 13.07.2002. - 15.07.2002
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
4-hydroxynonenal; hepatocytes; splenic cells
Sažetak
Although 4-hydroxynonenal (HNE) was first identified as highly cytotoxic product of lipid peroxidation, now it is believed that HNE is also cell growth modifier that plays role in signaling. Our previous results showed that spontaneously immortalized murine liver cells pretreated in vitro with cytotoxic concentration of HNE recover only if they are cultivated with spleen cells. One the other hand, oxidative stress was shown to play regulatory role during liver regeneration, while splenic cells infiltrate regenerating liver cells also having certain, not yet explained role in regulation of the liver regeneration. Hence, we wanted to see if this phenomenon would be repeated with cultured hepatocytes. For this purpose we have isolated hepatocytes from adult Fisher rat by the in situ two-step collagenase perfusion technique. Hepatocytes were treated with 1 µ ; M and 10 µ ; M HNE and were cultivated either with or without spleen cells. Cells were stained with DAPI, and then analyzed for micronuclei, mitotic index, apoptosis and necrosis. There were no differences if hepatocytes were treated with 1 µ ; M HNE, nor if they were cultivated alone or with spleen cells. However, if hepatocytes treated with 10 µ ; M HNE were co-cultivated with splenic cells, they showed significantly less apoptosis and necrosis then hepatocytes treated with 10 M only. These findings indicate possible novel regulatory mechanism of liver regeneration.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Javno zdravstvo i zdravstvena zaštita
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb