The in vivo positional identity gene expression code is not preserved in neural stem cells grown in culture

被引:47
作者
Santa-Olalla, J [1 ]
Baizabal, JM [1 ]
Fregoso, M [1 ]
Cárdenas, MD [1 ]
Covarrubias, L [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Inst Biotechnol, Dept Dev Genet & Mol Physiol, Cuernavaca 62250, Morelos, Mexico
关键词
growth factors; mouse; neurospheres; regional specification;
D O I
10.1046/j.1460-9568.2003.02824.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neural stem cell specification depends on antero-posterior (AP) and dorso-ventral (DV) information provided during development. In the present study we identified similar neural stem cell (NSC) populations along the AP axis of the mouse central nervous system: the 'early' NSCs responsive to fibroblast growth factor-2 and the 'late' NSCs responsive to epidermal growth factor (EGF). Gene expression analysis shows that AP and DV transcription factor code is not preserved in NSCs in culture. Neurospheres generated with EGF from different regions showed Emx2, En2 and Krox20 expression beyond their corresponding AP restricted areas (telencephalon, mesencephalon and rhomboencephalon, respectively). Hox genes were rarely expressed. DV markers such as Pax7 and Dbx1 were not expressed in neurosphere cells, whereas Pax6 and Nkx2.1 were highly expressed independently of the NSC source region. In general, this pattern was found under different culture conditions. We propose that signals surrounding NSCs determine their positional identity gene expression code, which may be relevant to establish their definitive fate.
引用
收藏
页码:1073 / 1084
页数:12
相关论文
共 72 条
[61]   INDEPENDENT ASSIGNMENT OF ANTERO-POSTERIOR AND DORSOVENTRAL POSITIONAL VALUES IN THE DEVELOPING CHICK HINDBRAIN [J].
SIMON, H ;
HORNBRUCH, A ;
LUMSDEN, A .
CURRENT BIOLOGY, 1995, 5 (02) :205-214
[62]  
SVENDSEN CN, 1995, EXP BRAIN RES, V102, P407
[63]   Direct neural fate specification from embryonic stem cells: A primitive mammalian neural stem cell stage acquired through a default mechanism [J].
Tropepe, V ;
Hitoshi, S ;
Sirard, C ;
Mak, TW ;
Rossant, J ;
van der Kooy, D .
NEURON, 2001, 30 (01) :65-78
[64]   Distinct neural stem cells proliferate in response to EGF and FGF in the developing mouse telencephalon [J].
Tropepe, V ;
Sibilia, M ;
Ciruna, BG ;
Rossant, T ;
Wagner, EF ;
van der Kooy, D .
DEVELOPMENTAL BIOLOGY, 1999, 208 (01) :166-188
[65]  
WALTHER C, 1991, DEVELOPMENT, V113, P1435
[66]  
Wassef M, 1997, PERSPECT DEV NEUROBI, V5, P3
[67]  
Weiss S, 1998, J NEUROBIOL, V36, P307, DOI 10.1002/(SICI)1097-4695(199808)36:2<307::AID-NEU14>3.0.CO
[68]  
2-A
[69]  
WURST W, 1994, DEVELOPMENT, V120, P2065
[70]   WINGED HELIX TRANSCRIPTION FACTOR BF-1 IS ESSENTIAL FOR THE DEVELOPMENT OF THE CEREBRAL HEMISPHERES [J].
XUAN, SH ;
BAPTISTA, CA ;
BALAS, G ;
TAO, WF ;
SOARES, VC ;
LAI, E .
NEURON, 1995, 14 (06) :1141-1152