Peripheral nerve-derived VEGF promotes arterial differentiation via neuropilin 1-mediated positive feedback

被引:196
作者
Mukouyama, YS
Gerber, HP
Ferrara, N
Gu, CH
Anderson, DJ
机构
[1] CALTECH, Div Biol 21676, Pasadena, CA 91125 USA
[2] CALTECH, Howard Hughes Med Inst, Pasadena, CA 91125 USA
[3] Genentech Inc, Dept Mol Oncol, San Francisco, CA 94080 USA
[4] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
来源
DEVELOPMENT | 2005年 / 132卷 / 05期
关键词
VEGF; neuropilin; 1; arterial differentiation; mouse;
D O I
10.1242/dev.01675
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In developing limb skin, peripheral nerves are required for arterial differentiation, and guide the pattern of arterial branching. In vitro experiments suggest that nerve-derived VEGF may be important for arteriogenesis, but its role in vivo remains unclear. Using a series of nerve-specific Cre lines, we show that VEGF derived from sensory neurons, motoneurons and/or Schwann cells is required for arteriogenesis in vivo. Arteriogenesis also requires endothelial expression of NRP1, an artery-specific coreceptor for VEGF(164) that is itself induced by VEGF. Our results provide the first evidence that VEGF is necessary for arteriogenesis from a primitive capillary plexus in vivo, and show that in limb skin the nerve is indeed the principal source of this signal. They also suggest a model in which a 'winner-takes-all' competition for VEGF may control arterial differentiation, with the outcome biased by a VEGF(164)-NRP1 positive-feedback loop. Our results also demonstrate that nerve-vessel alignment is a necessary, but not sufficient, condition for nerve-induced arteriogenesis. Different mechanisms therefore probably underlie these endothelial patterning and differentiation processes.
引用
收藏
页码:941 / 952
页数:12
相关论文
共 38 条
[1]   Radial glia serve as neuronal progenitors in all regions of the central nervous system [J].
Anthony, TE ;
Klein, C ;
Fishell, G ;
Heintz, N .
NEURON, 2004, 41 (06) :881-890
[2]   Neurovascular congruence results from a shared patterning mechanism that utilizes Semaphorin3A and Neuropilin-1 [J].
Bates, D ;
Taylor, GI ;
Minichiello, J ;
Farlie, P ;
Cichowitz, A ;
Watson, N ;
Klagsbrun, M ;
Mamluk, R ;
Newgreen, DF .
DEVELOPMENTAL BIOLOGY, 2003, 255 (01) :77-98
[3]   Impaired myocardial angiogenesis and ischemic cardiomyopathy in mice lacking the vascular endothelial growth factor isoforms VEGF164 and VEGF188 [J].
Carmeliet, P ;
Ng, YS ;
Nuyens, D ;
Theilmeier, G ;
Brusselmans, K ;
Cornelissen, I ;
Ehler, E ;
Kakkar, VV ;
Stalmans, I ;
Mattot, V ;
Perriard, JC ;
Dewerchin, M ;
Flameng, W ;
Nagy, A ;
Lupu, F ;
Moons, L ;
Collen, D ;
D'Amore, PA ;
Shima, DT .
NATURE MEDICINE, 1999, 5 (05) :495-502
[4]   Blood vessels and nerves: Common signals, pathways and diseases [J].
Carmeliet, P .
NATURE REVIEWS GENETICS, 2003, 4 (09) :710-720
[5]   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
[6]  
CLEAVER, 1999, HEART DEV, P223
[7]   Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase [J].
Danielian, PS ;
Muccino, D ;
Rowitch, DH ;
Michael, SK ;
McMahon, AP .
CURRENT BIOLOGY, 1998, 8 (24) :1323-1326
[8]   Dosage-sensitive requirement for mouse D114 in artery development [J].
Duarte, A ;
Hirashima, M ;
Benedito, R ;
Trindade, A ;
Diniz, P ;
Bekman, E ;
Costa, L ;
Henrique, D ;
Rossant, J .
GENES & DEVELOPMENT, 2004, 18 (20) :2474-2478
[9]   P0-Cre transgenic mice for inactivation of adhesion molecules in Schwann cells [J].
Feltri, ML ;
D'Antonio, M ;
Previtali, S ;
Fasolini, M ;
Messing, A ;
Wrabetz, L .
CHARCOT-MARIE-TOOTH DISORDERS, 1999, 883 :116-123
[10]   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