Vascular endothelial zinc finger 1 is involved in the regulation of angiogenesis: Possible contribution of stathmin/OP18 as a downstream target gene

被引:45
作者
Miyashita, H [1 ]
Kanemura, M [1 ]
Yamazaki, T [1 ]
Abe, M [1 ]
Sato, Y [1 ]
机构
[1] Tohoku Univ, Inst Dev Aging & Canc, Dept Vasc Biol, Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
Vezf1; transcription factor; endothelial cell; angiogenesis; stathmin/OP18;
D O I
10.1161/01.ATV.0000126373.52450.32
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective - Vascular endothelial zinc finger 1 (Vezf1) is a recently identified zinc finger transcription factor that is expressed in endothelial cells (ECs) during vascular development in mouse embryo. Here, we present that Vezf1 was expressed in ECs at the site of postnatal angiogenesis. We therefore examined whether Vezf1 was involved in the regulation of angiogenesis. Methods and Results - The specific downregulation of Vezf1 by antisense oligodeoxynucleotide (AS-ODN) significantly inhibited the proliferation, migration, and network formation of cultured ECs as well as angiogenesis in vivo. Vezf1 AS-ODN downregulated the expression of stathmin/oncoprotein18 (OP18), a microtubule-destabilizing protein, in ECs, whereas transient transfection of Vezf1 cDNA increased the expression of stathmin/OP18 in ECs. To explore the relationship between Vezf1 and stathmin/OP18, we specifically downregulated stathmin/OP18. We found that stathmin/OP18 AS-ODN inhibited the proliferation, migration, and network formation of ECs as Vezf1 AS-ODN did. Moreover, Vezf1 AS-ODN decreased G2/M population of ECs and increased apoptosis, which reproduced the characteristic feature of stathmin/OP18 inhibition. Conclusion - These results suggest that Vezf1 is involved in the regulation of angiogenesis, at least in part, through the expression of stathmin/OP18 in ECs.
引用
收藏
页码:878 / 884
页数:7
相关论文
共 40 条
[1]   Vezf1/DB1 is an endothelial cell-specific transcription factor that regulates expression of the endothelia-1 promoter [J].
Aitsebaomo, J ;
Kingsley-Kallesen, ML ;
Wu, YX ;
Quertermous, T ;
Patterson, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (42) :39197-39205
[2]   Mouse models in the study of the Ets family of transcription factors [J].
Bartel, FO ;
Higuchi, T ;
Spyropoulos, DD .
ONCOGENE, 2000, 19 (55) :6443-6454
[3]   Identification of a protein that interacts with tubulin dimers and increases the catastrophe rate of microtubules [J].
Belmont, LD ;
Mitchison, TJ .
CELL, 1996, 84 (04) :623-631
[4]  
Belotti D, 1996, CLIN CANCER RES, V2, P1843
[5]   Expression of stathmin and SCG10 proteins in the olfactory neurogenesis during development and after lesion in the adulthood [J].
Camoletto, P ;
Colesanti, A ;
Ozon, S ;
Sobel, A ;
Fasolo, A .
BRAIN RESEARCH BULLETIN, 2001, 54 (01) :19-28
[6]   Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele [J].
Carmeliet, P ;
Ferreira, V ;
Breier, G ;
Pollefeyt, S ;
Kieckens, L ;
Gertsenstein, M ;
Fahrig, M ;
Vandenhoeck, A ;
Harpal, K ;
Eberhardt, C ;
Declercq, C ;
Pawling, J ;
Moons, L ;
Collen, D ;
Risau, W ;
Nagy, A .
NATURE, 1996, 380 (6573) :435-439
[7]   Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene [J].
Ferrara, N ;
CarverMoore, K ;
Chen, H ;
Dowd, M ;
Lu, L ;
OShea, KS ;
PowellBraxton, L ;
Hillan, KJ ;
Moore, MW .
NATURE, 1996, 380 (6573) :439-442
[8]   ROLE OF THE FLT-1 RECEPTOR TYROSINE KINASE IN REGULATING THE ASSEMBLY OF VASCULAR ENDOTHELIUM [J].
FONG, GH ;
ROSSANT, J ;
GERTSENSTEIN, M ;
BREITMAN, ML .
NATURE, 1995, 376 (6535) :66-70
[9]   Symmetrical mutant phenotypes of the receptor EphB4 and its specific transmembrane ligand ephrin-B2 in cardiovascular development [J].
Gerety, SS ;
Wang, HU ;
Chen, ZF ;
Anderson, DJ .
MOLECULAR CELL, 1999, 4 (03) :403-414
[10]   The SCL gene specifies haemangioblast development from early mesoderm [J].
Gering, M ;
Rodaway, ARF ;
Göttgens, B ;
Patient, RK ;
Green, AR .
EMBO JOURNAL, 1998, 17 (14) :4029-4045