Anti-VEGFR-2 scFvs for cell isolation.: Single-chain antibodies recognizing the human vascular endothelial growth factor receptor-2 (VEGFR-2/flk-1) on the surface of primary endothelial cells and preselected.: CD34+ cells from cord blood

被引:34
作者
Böldicke, T
Tesar, M
Griesel, C
Rohde, M
Gröne, HJ
Waltenberger, J
Kollet, G
Lapidot, T
Yayon, A
Weich, H
机构
[1] German Res Ctr Biotechnol, Dept Appl Genet, D-38124 Braunschweig, Germany
[2] German Res Ctr Biotechnol, Div Microbiol, Braunschweig, Germany
[3] German Res Ctr Biotechnol, Dept Biochem Engn, Braunschweig, Germany
[4] German Res Ctr Biotechnol, Dept Gene Regulat & Differentiat, Braunschweig, Germany
[5] DKFZ, Inst Cellular & Mol Pathol, Heidelberg, Germany
[6] Univ Ulm, Med Ctr, Dept Internal Med 2, Ulm, Germany
[7] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[8] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
关键词
immune V-gene phage display library; single-chain antibody; human VEGF receptor 2; FACS analysis; hematopoitic stem cell;
D O I
10.1634/stemcells.19-1-24
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Five specific single-chain antibodies recognizing the human vascular endothelial growth factor receptor-2 (VEGFR-2/KDR) were selected from a V-gene phage display library constructed from mice immunized with the extracellular domain of VEGFR-2 (Tg-like domain 1-7), hll five scFv antibodies (A3, A7, B11, G3, and H1) bound to the purified native antigen in enzyme-linked immunosorbent assay and Dot Blot, and showed no crossreactivity to the human VEGF-receptor 1 (VEGFR-1). The selected antibodies recognize a conformation-dependent epitope of the native receptor and do not recognize denatured antigen in Western blots, as well as linear overlapping peptides comprising the sequence of the human VEGFR-2. The five scFv antibodies bind to the surface of endothelial cells overexpressing human VEGFR-2 c-DNA (PAE/VEGFR-2 cells) as detected by surface immunofluorescence using confocal microscopy. In addition scFv A7 specifically detected VEGFR-2 expresring endothelial cells in the glomerulus of frozen human kidney tissue sections. Therefore, A7 has potential clinical application as a marker for angiogenesis in cryosections of different human tissues. Additionally, two recombinant scFvs (A2 and A7) very efficiently recognize VEGFR-2 on PAE/VEGFR-2 cells and freshly prepared human umbilical vein endothelial cells by fluorescence-activated cell sorter (FACS) analysis. The scFv fragment A7, which was the most sensitive antibody in FAGS analysis, recognizes human CD34*VEGFR-2* hematopoietic immature cells within the population of enriched CD34(+) cells isolated from human cord blood. The dissociation constant of A7 mas determined to be K-d = 3.8 x 10(-9) M by BIAcore analysis, In conclusion, scFv fragment A7 scents to be an important tool for FAGS analysis and cell sorting of vascular endothelial cells, progenitor cells and hematopoitic stem cells, which are positive for VEGFR-2 gene expression.
引用
收藏
页码:24 / 36
页数:13
相关论文
共 37 条
[1]   The angiogenesis induced by HIV-1 Tat protein is mediated by the Flk-1/KDR receptor on vascular endothelial cells [J].
Albini, A ;
Soldi, R ;
Giunciuglio, D ;
Giraudo, E ;
Benelli, R ;
Primo, L ;
Noonan, D ;
Salio, M ;
Camussi, G ;
Rockl, W ;
Bussolino, F .
NATURE MEDICINE, 1996, 2 (12) :1371-1375
[2]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[3]   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
[4]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[5]   MAKING ANTIBODY FRAGMENTS USING PHAGE DISPLAY LIBRARIES [J].
CLACKSON, T ;
HOOGENBOOM, HR ;
GRIFFITHS, AD ;
WINTER, G .
NATURE, 1991, 352 (6336) :624-628
[6]  
DELIA D, 1993, BLOOD, V81, P1001
[7]   Ligand-dependent development of the endothelial and hemopoietic lineages from embryonic mesodermal cells expressing vascular endothelial growth factor receptor 2 [J].
Eichmann, A ;
Corbel, C ;
Nataf, V ;
Vaigot, P ;
Breant, C ;
LeDouarin, NM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5141-5146
[8]   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
[9]   The biology of vascular endothelial growth factor [J].
Ferrara, N ;
DavisSmyth, T .
ENDOCRINE REVIEWS, 1997, 18 (01) :4-25
[10]   Antibody phage display technology and its applications [J].
Hoogenboom, HR ;
de Bruine, AP ;
Hufton, SE ;
Hoet, RM ;
Arends, JW ;
Roovers, RC .
IMMUNOTECHNOLOGY, 1998, 4 (01) :1-20