Endothelial growth factor receptors in human fetal heart

被引:38
作者
Partanen, TA
Makinen, T
Arola, J
Suda, T
Weich, HA
Alitalo, K
机构
[1] Univ Helsinki, Haartman Inst, Mol Canc Biol Lab, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Haartman Inst, Dept Pathol, FIN-00014 Helsinki, Finland
[3] Kumamoto Univ, Sch Med, Dept Cell Differentiat, Kumamoto 860, Japan
[4] Natl Res Ctr Biotechnol, Dept Gene Regulat & Different, Div Mol Biotechnol, Braunschweig, Germany
关键词
angiogenesis; endothelium; endocardium; myocardium; growth substances;
D O I
10.1161/01.CIR.100.6.583
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Endothelial receptor tyrosine kinases include 3 members of the vascular endothelial growth factor receptor (VEGFR) family and 2 members of the angiopoietin receptor (Tie) family. In addition, the VEGF(165) isoform binds to neuropilin-1 (NP-1), a receptor for collapsins/semaphorins. The importance of these receptors for vasculogenesis and angiogenesis has been shown in gene-targeted mice, but so far, little is known about their exact expression patterns in the human vasculature. Methods and Results-Frozen sections of human fetal heart were stained immunohistochemically with receptor-specific monoclonal (VEGFR, Tie) or polyclonal (NP-1) antibodies. The following patterns were observed: The endocardium was positive for VEGFR-1, VEGFR-2, NP-I, Tie-1, and Tie-2 but negative for VECFR-3. The coronary vessels were positive for Tie-1, Tie-2, VEGFR-1, and NP-1 and negative for VEGFR-2 and VEGFR-3. Myocardial capillaries and epicardial blood vessels stained for VEGFR-1, VEGFR-2, NP-1, and Tie-1; myocardial capillaries and epicardial veins weakly for Tie-2; and epicardial lymphatic vessels for VEGFR-2 and VEGFR-3, weakly for Tie-1 and Tie-2, but not for VEGFR-1 or NP-1. Conclusions-The results demonstrate differential expression of the endothelial growth factor receptors in distinct types of vessels in the human heart. This information is useful for the understanding of their roles in physiological and pathological processes and for their diagnostic and therapeutic application in cardiovascular medicine.
引用
收藏
页码:583 / 586
页数:4
相关论文
共 20 条
[1]   Tie2 receptor ligands, angiopoietin-1 and angiopoietin-2, modulate VEGF-induced postnatal neovascularization [J].
Asahara, T ;
Chen, DH ;
Takahashi, T ;
Fujikawa, K ;
Kearney, M ;
Magner, M ;
Yancopoulos, GD ;
Isner, JM .
CIRCULATION RESEARCH, 1998, 83 (03) :233-240
[2]  
Baumgartner I, 1998, VASA-J VASCULAR DIS, V27, P201
[3]   VASCULARIZATION OF THE MOUSE EMBRYO - A STUDY OF FLK-1, TEK, TIE, AND VASCULAR ENDOTHELIAL GROWTH-FACTOR EXPRESSION DURING DEVELOPMENT [J].
DUMONT, DJ ;
FONG, GH ;
PURI, MC ;
GRADWOHL, G ;
ALITALO, K ;
BREITMAN, ML .
DEVELOPMENTAL DYNAMICS, 1995, 203 (01) :80-92
[4]   Cardiovascular failure in mouse embryos deficient in VEGF receptor-3 [J].
Dumont, DJ ;
Jussila, L ;
Taipale, J ;
Lymboussaki, A ;
Mustonen, T ;
Pajusola, K ;
Breitman, M ;
Alitalo, K .
SCIENCE, 1998, 282 (5390) :946-949
[5]   DOMINANT-NEGATIVE AND TARGETED NULL MUTATIONS IN THE ENDOTHELIAL RECEPTOR TYROSINE KINASE, TEK, REVEAL A CRITICAL ROLE IN VASCULOGENESIS OF THE EMBRYO [J].
DUMONT, DJ ;
GRADWOHL, G ;
FONG, GH ;
PURI, MC ;
GERTSENSTEIN, M ;
AUERBACH, A ;
BREITMAN, ML .
GENES & DEVELOPMENT, 1994, 8 (16) :1897-1909
[6]  
Ferrara N, 1999, CURR TOP MICROBIOL, V237, P1
[7]   A recombinant mutant vascular endothelial growth factor-C that has lost vascular endothelial growth factor receptor-2 binding, activation, and vascular permeability activities [J].
Joukov, V ;
Kumar, V ;
Sorsa, T ;
Arighi, E ;
Weich, H ;
Saksela, O ;
Alitalo, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (12) :6599-6602
[8]  
Jussila L, 1998, CANCER RES, V58, P1599
[9]   THE RELATED FLT4, FLT1, AND KDR RECEPTOR TYROSINE KINASES SHOW DISTINCT EXPRESSION PATTERNS IN HUMAN FETAL ENDOTHELIAL-CELLS [J].
KAIPAINEN, A ;
KORHONEN, J ;
PAJUSOLA, K ;
APRELIKOVA, O ;
PERSICO, MG ;
TERMAN, BI ;
ALITALO, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (06) :2077-2088
[10]  
Kitsukawa T, 1995, DEVELOPMENT, V121, P4309