Crucial role of the small GTPase ARF6 in hepatic cord formation during liver development

被引:62
作者
Suzuki, Teruhiko
Kanai, Yoshiakira
Hara, Takahiko
Sasaki, Junko
Sasaki, Takehiko
Kohara, Michinori
Maehama, Tomohiko
Taya, Choji
Shitara, Hiroshi
Yonekawa, Hiromichi
Frohman, Michael A.
Yokozeki, Takeaki
Kanaho, Yasunori
机构
[1] Univ Tsukuba, Grad Sch Comprehens Human Sci, Dept Physiol Chem, Tsukuba, Ibaraki 3058575, Japan
[2] Univ Tsukuba, Inst Basic Med Sci, Tsukuba, Ibaraki 3058575, Japan
[3] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Physiol Chem, Bunkyo Ku, Tokyo 1130033, Japan
[4] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Vet Anat, Bunkyo Ku, Tokyo 1138657, Japan
[5] Tokyo Metropolitan Inst Med Sci, Lab Mouse Model Human Heritable Dis, Infect Dis Project, Bunkyo Ku, Tokyo 1138613, Japan
[6] Tokyo Metropolitan Inst Med Sci, Lab Mouse Model Human Heritable Dis, Biomembrane Signalling Project, Bunkyo Ku, Tokyo 1138613, Japan
[7] Tokyo Metropolitan Inst Med Sci, Lab Mouse Model Human Heritable Dis, Core Technol & Res Ctr, Bunkyo Ku, Tokyo 1138613, Japan
[8] Tokyo Metropolitan Inst Med Sci, Lab Mouse Model Human Heritable Dis, Stem Cell Project, Bunkyo Ku, Tokyo 1138613, Japan
[9] Akita Univ, Sch Med, Dept Pathol & Immunol, Akita 0108543, Japan
[10] SUNY Stony Brook, Ctr Dev Genet, Stony Brook, NY 11794 USA
[11] SUNY Stony Brook, Dept Pharmacol, Stony Brook, NY 11794 USA
关键词
D O I
10.1128/MCB.00298-06
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 mammalian small GTPase ADP-ribosylation factor 6 (ARF6) plays important roles in a wide variety of cellular events, including endocytosis, actin cytoskeletal reorganization, and phosphoinositide metabolism. However, physiological functions for ARF6 have not previously been examined. Here, we described the consequence of ARF6 ablation in mice, which manifests most obviously in the context of liver development. Livers from ARF6(-/-) embryos are smaller and exhibit hypocellularity, due to the onset of midgestational liver cell apoptosis. Preceding the apoptosis, however, defective hepatic cord formation is observed; the liver cells migrate abnormally upon exiting the primordial hepatic epithelial sheet and clump rather than becoming dispersed. Consistent with this observation, the ability of hepatocyte growth factor/scatter factor (HGF) to induce hepatic cord-like structures from ARF6(-/-) fetal hepatocytes cultured in vitro in collagen gel matrix is impaired. Finally, we show that endogenous ARF6 in wild-type fetal hepatocytes is activated in response to HGF stimulation. These results provide evidence that ARF6 is an essential component in the signaling pathway coupling HGF signaling to hepatic cord formation.
引用
收藏
页码:6149 / 6156
页数:8
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