Distinct neural stem cells proliferate in response to EGF and FGF in the developing mouse telencephalon

被引:678
作者
Tropepe, V
Sibilia, M
Ciruna, BG
Rossant, T
Wagner, EF
van der Kooy, D
机构
[1] Univ Toronto, Dept Anat & Cell Biol, Neurobiol Res Grp, Toronto, ON M5S 1A8, Canada
[2] Res Inst Mol Pathol, A-1030 Vienna, Austria
[3] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[4] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5S 1A8, Canada
[5] Univ Toronto, Dept Obstet & Gynecol, Toronto, ON M5S 1A8, Canada
基金
英国医学研究理事会;
关键词
EGF; FGF2; mouse; neural development; neural stem cells; proliferation; telencephalon;
D O I
10.1006/dbio.1998.9192
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multipotent, self-renewing neural stem cells reside in the embryonic mouse telencephalic germinal zone. Using an in vitro neurosphere assay for neural stem cell proliferation, we demonstrate that FGF-responsive neural stem cells are present as early as E8.5 in the anterior neural plate, but EGF-responsive neural stem cells emerge later in development in a temporally and spatially specific manner. By separately blocking EGF and FGF2 signaling, we also show that EGF alone and FGF2 alone can independently elicit neural stem cell proliferation and at relatively high cell densities separate cell nonautonomous effects can substantially enhance the mitogen-induced proliferation. At lower cell densities, neural stem cell proliferation is additive in the presence of EGF and FGF2 combined, revealing two different stem cell populations. However both FGF-responsive and EGF-responsive neural stem cells retain their self-renewal and multilineage potential, regardless of growth factor conditions. These results support a model in which separate, lineage-related EGF- and FGF-responsive neural stem cells are present in the embryonic telencephalic germinal zone, (C) 1999 Academic Press.
引用
收藏
页码:166 / 188
页数:23
相关论文
共 79 条
[1]  
AHMED S, 1995, J NEUROSCI, V15, P5765
[2]   EGF AND TGF-ALPHA STIMULATE RETINAL NEUROEPITHELIAL CELL-PROLIFERATION INVITRO [J].
ANCHAN, RM ;
REH, TA ;
ANGELLO, J ;
BALLIET, A ;
WALKER, M .
NEURON, 1991, 6 (06) :923-936
[3]  
Arsenijevic Y, 1998, J NEUROSCI, V18, P2118
[4]   Dorsal and ventral cell types can arise from common neural tube progenitors [J].
Artinger, KB ;
Fraser, S ;
BronnerFraser, M .
DEVELOPMENTAL BIOLOGY, 1995, 172 (02) :591-601
[5]   CELL-DEATH IN THE OLIGODENDROCYTE LINEAGE [J].
BARRES, BA ;
HART, IK ;
COLES, HSR ;
BURNE, JF ;
VOYVODIC, JT ;
RICHARDSON, WD ;
RAFF, MC .
JOURNAL OF NEUROBIOLOGY, 1992, 23 (09) :1221-1230
[6]   DETERMINATION OF NUMBERS OF OSTEOPROGENITORS PRESENT IN ISOLATED FETAL-RAT CALVARIA CELLS-INVITRO [J].
BELLOWS, CG ;
AUBIN, JE .
DEVELOPMENTAL BIOLOGY, 1989, 133 (01) :8-13
[7]   HEPARAN SULFATES MEDIATE THE BINDING OF BASIC FIBROBLAST GROWTH-FACTOR TO A SPECIFIC RECEPTOR ON NEURAL PRECURSOR CELLS [J].
BRICKMAN, YG ;
FORD, MD ;
SMALL, DH ;
BARTLETT, PF ;
NURCOMBE, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :24941-24948
[8]   Response diversity and the timing of progenitor cell maturation are regulated by developmental changes in EGFR expression in the cortex [J].
Burrows, RC ;
Wancio, D ;
Levitt, P ;
Lillien, L .
NEURON, 1997, 19 (02) :251-267
[9]  
Ciruna BG, 1997, DEVELOPMENT, V124, P2829
[10]  
Craig CG, 1996, J NEUROSCI, V16, P2649