Expression of VE-cadherin in zebrafish embryos:: A new tool to evaluate vascular development

被引:87
作者
Larson, JD
Wadman, SA
Chen, E
Kerley, L
Clark, KJ
Eide, M
Lippert, S
Nasevicius, A
Ekker, SC
Hackett, PB
Essner, JJ
机构
[1] Discovery Genom Inc, Minneapolis, MN USA
[2] Univ Minnesota, Arnold & Mabel Beckman Ctr Transposon Res, Dept Genet Cell Biol & Dev, Minneapolis, MN USA
[3] Univ Minnesota, Mol Cellular Dev Biol & Genet Grad Program, Minneapolis, MN USA
关键词
VE-cadherin; zebrafish; vasculature; vascular endothelial cell; endocardium; vertebrate; angiogenesis;
D O I
10.1002/dvdy.20102
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
We have identified the zebrafish homologue of VE-cadherin and documented its expression in the developing vascular system. The zebrafish VE-cadherin gene is specifically expressed in the vascular endothelial cell lineage beginning with the differentiation and migration of angioblasts and persists throughout vasculogenesis, angiogenesis, and endocardium development. Staining zebrafish embryos by whole-mount in situ hybridization with the VE-cadherin probe provides a method to screen embryos for vascular defects. To illustrate this utility, we used VE-cadherin expression to demonstrate a conservation of vascular endothelial growth factor-A (VEGF-A) function. The morpholino antisense oligonucleotide knockdown of VEGF-A function in zebrafish embryos results in a loss of angiogenic blood vessels, as indicated by the lack of VE-cadherin expression in the intersegmental vasculature. This loss can be restored in embryos supplemented with either zebrafish or human VEGF-A, the latter indicating that genes crucial to angiogenesis have highly conserved functional activities in vertebrates. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:204 / 213
页数:10
相关论文
共 32 条
[11]   Molecular and biological properties of vascular endothelial growth factor [J].
Ferrara, N .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1999, 77 (07) :527-543
[12]   Blood vessel formation: What is its molecular basis? [J].
Folkman, J ;
DAmore, PA .
CELL, 1996, 87 (07) :1153-1155
[13]   Vessel patterning in the embryo of the zebrafish: Guidance by notochord [J].
Fouquet, B ;
Weinstein, BM ;
Serluca, FC ;
Fishman, MC .
DEVELOPMENTAL BIOLOGY, 1997, 183 (01) :37-48
[14]  
Gibbs PDL, 2000, MAR BIOTECHNOL, V2, P107
[15]   Analysis of a zebrafish VEGF receptor mutant reveals specific disruption of angiogenesis [J].
Habeck, H ;
Odenthal, J ;
Walderich, B ;
Maischien, HM ;
Schulte-Merker, S .
CURRENT BIOLOGY, 2002, 12 (16) :1405-1412
[16]   IDENTIFICATION OF A CA-2+-DEPENDENT CELL CELL-ADHESION MOLECULE IN ENDOTHELIAL-CELLS [J].
HEIMARK, RL ;
DEGNER, M ;
SCHWARTZ, SM .
JOURNAL OF CELL BIOLOGY, 1990, 110 (05) :1745-1756
[17]   Angiogenic network formation in the developing vertebrate trunk [J].
Isogai, S ;
Lawson, ND ;
Torrealday, S ;
Horiguchi, M ;
Weinstein, BM .
DEVELOPMENT, 2003, 130 (21) :5281-5290
[18]   The vascular anatomy of the developing zebrafish: An atlas of embryonic and early larval development [J].
Isogai, S ;
Horiguchi, M ;
Weinstein, BM .
DEVELOPMENTAL BIOLOGY, 2001, 230 (02) :278-301
[19]   A NOVEL ENDOTHELIAL-SPECIFIC MEMBRANE-PROTEIN IS A MARKER OF CELL CELL CONTACTS [J].
LAMPUGNANI, MG ;
RESNATI, M ;
RAITERI, M ;
PIGOTT, R ;
PISACANE, A ;
HOUEN, G ;
RUCO, LP ;
DEJANA, E .
JOURNAL OF CELL BIOLOGY, 1992, 118 (06) :1511-1522
[20]   In vivo imaging of embryonic vascular development using transgenic zebrafish [J].
Lawson, ND ;
Weinstein, BM .
DEVELOPMENTAL BIOLOGY, 2002, 248 (02) :307-318