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Transforming growth factor α protects against Fas-mediated liver apoptosis in mice
被引:13
|作者:
Kanda, D
[1
]
Takagi, H
[1
]
Toyoda, M
[1
]
Horiguchi, N
[1
]
Nakajima, H
[1
]
Otsuka, T
[1
]
Mori, M
[1
]
机构:
[1] Gunma Univ, Sch Med, Dept Internal Med 1, Maebashi, Gumma 3718511, Japan
关键词:
Fas/APO-1/CD95;
apoptosis;
transforming growth factor alpha;
Bcl-xL;
D O I:
10.1016/S0014-5793(02)02677-7
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The Fas/Fas ligand interaction plays a crucial role in various liver diseases, and administration of agonistic anti-Fas antibody to mice causes massive hepatic apoptosis and fulminant hepatic failure. Several growth factors have recently been found to function in preventing apoptosis. In this study, we demonstrated that overexpression of transforming growth factor alpha (TGFalpha) has a dramatic protective effect on Fas-mediated hepatic apoptosis at the biochemical and histological levels. Moreover, 85.7% (six out of seven) of TGFalpha transgenic mice survived the lethal liver damage, whereas all wild-type mice died. Expression of Bel-xL, an anti-apoptotic protein, was greatly increased in the transgenic mice. Taken together, our findings suggest that TGFalpha protects against Fas-mediated liver apoptosis in vivo and up-regulation of Bel-xL may participate in protective effect of TGFalpha. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
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页码:11 / 15
页数:5
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