Telencephalic progenitors maintain anteroposterior identities cell autonomously

被引:35
作者
Na, E
McCarthy, M
Neyt, C
Lai, E
Fishell, G
机构
[1] NYU, Med Ctr, Dev Genet Program, New York, NY 10016 USA
[2] NYU, Med Ctr, Dept Cell Biol, Skirball Inst Biomol Med, New York, NY 10016 USA
[3] Mem Sloan Kettering Canc Ctr, Cell Biol Program, New York, NY 10021 USA
关键词
D O I
10.1016/S0960-9822(98)70403-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Grafting experiments have demonstrated that determination of anteroposterior (AP) identity is an early step in neural patterning that precedes dorsoventral (DV) specification [1,2]. These studies used pieces of tissue, however, rather than individual cells to address this question. It thus remains unclear whether the maintenance of AP identity is a cell-autonomous property or a result of signaling between cells within the grafted tissue. Previously, we and others [3-5] have used transplants of dissociated brain cells to show that individual telencephalic precursor cells can adopt host-specific DV identities when they integrate within novel regions of the telencephalon. We have now undertaken a set of transplantations during the same mid-neurogenic period used in the previous studies to assess the ability of telencephalic progenitors to integrate and differentiate into more posterior regions of the neuraxis, We observed that telencephalic progenitors were capable of integrating and migrating within different AP levels of the central nervous system (CNS). Despite this, we found that telencephalic progenitors that integrated within the diencephalon and the mesencephalon continued to express a telencephalic marker until adulthood. We speculate that during neurogenesis individual progenitors are determined in terms of their AP but not their DV identity, Hence, AP identity is maintained cell autonomously within individual progenitors.
引用
收藏
页码:987 / 990
页数:4
相关论文
共 23 条
[1]  
BAYER SA, 1989, NEUROTOXICOLOGY, V10, P307
[2]   Host-guided migration allows targeted introduction of neurons into the embryonic brain [J].
Brustle, O ;
Maskos, U ;
McKay, RDG .
NEURON, 1995, 15 (06) :1275-1285
[3]   Regional incorporation and site-specific differentiation of striatal precursors transplanted to the embryonic forebrain ventricle [J].
Campbell, K ;
Olsson, M ;
Bjorklund, A .
NEURON, 1995, 15 (06) :1259-1273
[4]   A SHORT-TERM ANALYSIS OF THE BEHAVIOR OF CONDITIONALLY IMMORTALIZED NEURONAL PROGENITORS AND PRIMARY NEUROEPITHELIAL CELLS IMPLANTED INTO THE FETAL-RAT BRAIN [J].
CATTANEO, E ;
MAGRASSI, L ;
BUTTI, G ;
SANTI, L ;
GIAVAZZI, A ;
PEZZOTTA, S .
DEVELOPMENTAL BRAIN RESEARCH, 1994, 83 (02) :197-208
[5]  
FISHELL G, 1995, DEVELOPMENT, V121, P803
[6]  
FOSTER GA, 1987, J NEUROSCI, V7, P1994
[7]  
GRAYBIEL AM, 1989, J NEUROSCI, V9, P3250
[8]   A COMMUNITY EFFECT IN ANIMAL DEVELOPMENT [J].
GURDON, JB .
NATURE, 1988, 336 (6201) :772-774
[9]   COMMUNITY EFFECTS AND RELATED PHENOMENA IN DEVELOPMENT [J].
GURDON, JB ;
LEMAIRE, P ;
KATO, K .
CELL, 1993, 75 (05) :831-834
[10]   MONOCLONAL M6 ANTIBODY INTERFERES WITH NEURITE EXTENSION OF CULTURED NEURONS [J].
LAGENAUR, C ;
KUNEMUND, V ;
FISCHER, G ;
FUSHIKI, S ;
SCHACHNER, M .
JOURNAL OF NEUROBIOLOGY, 1992, 23 (01) :71-88