Defective vascular morphogenesis and mid-gestation in mice lacking RA-GEF-1

被引:22
作者
Wei, Ping
Satoh, Takaya
Edamatsu, Hironori
Aiba, Atsu
Setsu, Tomiyoshi
Terashima, Toshio
Kitazawa, Sohei
Nakao, Kazuki
Yoshikawa, Yoko
Tamada, Masako
Kataoka, Tohru
机构
[1] Kobe Univ, Grad Sch Med, Dept Biochem & Mol Biol, Div Mol Biol,Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Kobe Univ, Grad Sch Med, Dept Physiol & Cell Biol, Div Mol Genet,Chuo Ku, Kobe, Hyogo 6500017, Japan
[3] Kobe Univ, Grad Sch Med, Dept Physiol & Cell Biol, Div Dev Neurobiol,Chuo Ku, Kobe, Hyogo 6500017, Japan
[4] Kobe Univ, Grad Sch Med, Dept Pathol & Microbiol, Div Mol Pathol,Chuo Ku, Kobe, Hyogo 6500017, Japan
[5] Riken Ctr Dev Biol, Lab Anim Resources & Genet Engn, Kobe, Hyogo 6500047, Japan
关键词
angiogenesis; embryonic lethality; knockout mouse; RA-GEF-1; Rap1; vasculogenesis;
D O I
10.1016/j.bbrc.2007.08.149
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
A multitude of guanine nucleotide exchange factors (GEFs) regulate Rap1 small GTPases, however, their individual functions remain obscure. Here, we investigate the in vivo function of the Rap1 GEF RA-GEF-1. The expression of RA-GEF-1 in wild-type mice starts at embryonic day (E) 8.5, and continues thereafter. RA-GEF-1(-/-) mice appear normal until E7.5, but become grossly abnormal and dead by E9.5. This mid-gestation death appears to be closely associated with severe defects in yolk sac blood vessel formation. RA-GEF-1(-/-) yolk sacs form apparently normal blood islands by E8.5, but the blood islands fail to coalesce into a primary vascular plexus, indicating that vasculogenesis is impaired. Furthermore, RA-GEF-1(-/-) embryos proper show severe defects in the formation of major blood vessels. These results suggest that deficient Rap1 signaling may lead to defective vascular morphogenesis in the yolk sac and embryos proper. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:106 / 112
页数:7
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