TAL1/SCL is expressed in endothelial progenitor cells angioblasts and defines a dorsal-to-ventral gradient of vasculogenesis

被引:135
作者
Drake, CJ [1 ]
Brandt, SJ
Trusk, TC
Little, CD
机构
[1] Med Univ S Carolina, Dept Cell Biol, Charleston, SC 29425 USA
[2] Med Univ S Carolina, Cardiovasc Dev Biol Ctr, Charleston, SC 29425 USA
[3] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Med Ctr, Dept Cell Biol, Nashville, TN 37232 USA
[5] Dept Vet Affairs Med Ctr, Nashville, TN 37232 USA
关键词
TAL1/SCL; vasculogenesis; endothelial lineage; angioblasts;
D O I
10.1006/dbio.1997.8751
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this study we establish that TAL1/SCL, a member of the helix-loop-helix family of transcription factors, and an important regulator of the hematopoietic lineage in mice, is expressed in the endothelial lineage of avians. The earliest events of vascular development were examined using antibodies to TAL1/SCL, and the QH1 antibody, an established marker of quail endothelial cells. Analyses using double immunofluorescence confocal microscopy show that: (i) TAL1/SCL is expressed by both quail and chicken endothelial cells; (ii) TAL1/SCL expression precedes that of the QH1 epitope; and (iii) TAL1/SCL, but not QH1, expression defines a subpopulation of primordial cells within the splanchnic mesoderm. Collectively these data suggest that TAL1/SCL-positive/QH1-negative cells are angioblasts. Further, using TAL1/SCL expression as a marker of the endothelial lineage, we demonstrate that in addition to the previously described cranial-to-caudal gradient, there is a dorsal-to-ventral progression of vasculogenesis. (C) 1997 Academic Press.
引用
收藏
页码:17 / 30
页数:14
相关论文
共 50 条
[1]   THE SCL GENE IS FORMED FROM A TRANSCRIPTIONALLY COMPLEX LOCUS [J].
APLAN, PD ;
BEGLEY, CG ;
BERTNESS, V ;
NUSSMEIER, M ;
EZQUERRA, A ;
COLIGAN, J ;
KIRSCH, IR .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (12) :6426-6435
[2]   Molecular cloning and expression of murine vascular endothelial cadherin in early stage development of cardiovascular system [J].
Breier, G ;
Breviario, F ;
Caveda, L ;
Berthier, R ;
Schnurch, H ;
Gotsch, U ;
Vestweber, D ;
Risau, W ;
Dejana, E .
BLOOD, 1996, 87 (02) :630-641
[3]   Geometric control of cell life and death [J].
Chen, CS ;
Mrksich, M ;
Huang, S ;
Whitesides, GM ;
Ingber, DE .
SCIENCE, 1997, 276 (5317) :1425-1428
[4]   Extracellular matrix rigidity causes strengthening of integrin-cytoskeleton linkages [J].
Choquet, D ;
Felsenfeld, DP ;
Sheetz, MP .
CELL, 1997, 88 (01) :39-48
[5]  
COCKERILL GW, 1995, INT REV CYTOL, V159, P113, DOI 10.1016/S0074-7696(08)62106-3
[6]  
COFFIN JD, 1988, DEVELOPMENT, V102, P735
[7]   DIFFUSE INTRAEMBRYONIC HEMATOPOIESIS IN NORMAL AND CHIMERIC AVIAN DEVELOPMENT [J].
DIETERLENLIEVRE, F ;
MARTIN, C .
DEVELOPMENTAL BIOLOGY, 1981, 88 (01) :180-191
[8]   VECTORS THAT FACILITATE THE EXPRESSION AND PURIFICATION OF FOREIGN PEPTIDES IN ESCHERICHIA-COLI BY FUSION TO MALTOSE-BINDING PROTEIN [J].
DIGUAN, C ;
LI, P ;
RIGGS, PD ;
INOUYE, H .
GENE, 1988, 67 (01) :21-30
[9]   ANTIBODIES TO BETA-1-INTEGRINS CAUSE ALTERATIONS OF AORTIC VASCULOGENESIS, INVIVO [J].
DRAKE, CJ ;
DAVIS, LA ;
LITTLE, CD .
DEVELOPMENTAL DYNAMICS, 1992, 193 (01) :83-91
[10]   A SURVEY BY SCANNING ELECTRON-MICROSCOPY OF THE EXTRACELLULAR-MATRIX AND ENDOTHELIAL COMPONENTS OF THE PRIMORDIAL CHICK HEART [J].
DRAKE, CJ ;
JACOBSON, AG .
ANATOMICAL RECORD, 1988, 222 (04) :391-400