In vitro and in vivo bioactivity of recombinant canine hepatocyte growth factor

被引:5
作者
Arends, Brigitte [1 ]
Spee, Bart [1 ,5 ]
Hoffmann, Gaby [1 ]
Jansen, Georgina E. G. [1 ]
Slump, Estel [1 ]
Auriemma, Edoardo [1 ]
IJzer, Jooske [2 ]
Hemrika, Wieger [3 ]
Romijn, Roland A. [3 ]
van der Heijden-Liefkens, Karin H. A. [4 ]
Sondermeijer, Paul J. A. [4 ]
van den Ingh, Ted S. G. A. M. [1 ]
Penning, Louis C. [1 ]
Rothuizen, Jan [1 ]
机构
[1] Univ Utrecht, Dept Clin Sci Compan Anim, Fac Vet Med, NL-3584 CM Utrecht, Netherlands
[2] Univ Utrecht, Fac Vet Med, Dept Pathobiol, NL-3584 CL Utrecht, Netherlands
[3] Univ Utrecht, ABC Prot Express Ctr, NL-3584 CH Utrecht, Netherlands
[4] Intervet Int, NL-5830 AA Boxmeer, Netherlands
[5] Katholieke Univ Leuven Hosp, Dept Mol Pathol, B-3000 Louvain, Belgium
关键词
HGF; c-MET; PKB; ERK1/2; PCNA; Partial hepatectomy; Liver regeneration; Dogs;
D O I
10.1016/j.tvjl.2007.11.002
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Hepatocyte growth factor (HGF) is crucial for the development and regeneration of the liver and offers a possible new therapeutic strategy for the treatment of canine liver disease. In this study, the in vitro and in vivo bioactivity of recombinant canine HGF (rcHGF) produced with a baculoviral expression system in insect cells was measured. In vitro rcHGF induced mitogenesis, motogenesis, and phosphorylated the HGF receptor c-MET and its downstream mediators PKB and ERK1/2 in two canine epithelial cell lines. After a partial hepatectomy (phx) in dogs, rcHGF increased phosphorylation of c-MET, PKB and ERK1/2. A moderate increase was seen with the cell cycle protein PCNA in rcHGF treated livers, but no HGF-induced increase in liver weight was seen 7 days after phx. Furthermore, rcHGF treated livers showed lower levels of the key mediator of apoptosis, caspase-3, at 7 days after phx. It is concluded that rcHGF is a biologically active protein in vitro and in vivo and the baculoviral expression system supplies sufficient amounts of rcHGF for future clinical studies in dogs. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:70 / 77
页数:8
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