Proliferative cell types in embryonic lineages of the central complex of the grasshopper Schistocerca gregaria

被引:21
作者
Boyan, George [1 ]
Williams, Leslie [1 ]
Legl, Andrea [1 ]
Herbert, Zsofia [1 ]
机构
[1] Univ Munich, Biozentrum, Dev Neurobiol Grp, D-82152 Planegg Martinsried, Germany
关键词
Development; Brain; Lineages; Mitosis; Insect; Schistocerca gregaria (Insecta); CENTRAL-NERVOUS-SYSTEM; AMPLIFYING NEUROBLAST LINEAGES; NEURONAL PRECURSOR CELLS; MUSHROOM BODIES; DROSOPHILA-MELANOGASTER; INSECT BRAIN; IDENTIFIED NEURONS; TEMPORAL PATTERNS; UNEQUAL DIVISION; EARLY EVENTS;
D O I
10.1007/s00441-010-0992-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The central complex of the grasshopper Schistocerca gregaria develops to completion during embryogenesis. A major cellular contribution to the central complex is from the w, x, y, z lineages of the pars intercerebralis, each of which comprises over 100 cells, making them by far the largest in the embryonic protocerebrum. Our focus has been to find a cellular mechanism that allows such a large number of cell progeny to be generated within a restricted period of time. Immunohistochemical visualization of the chromosomes of mitotically active cells has revealed an almost identical linear array of proliferative cells present simultaneously in each w, x, y, z lineage at 50% of embryogenesis. This array is maintained relatively unchanged until almost 70% of embryogenesis, after which mitotic activity declines and then ceases. The array is absent from smaller lineages of the protocerebrum not associated with the central complex. The proliferative cells are located apically to the zone of ganglion mother cells and amongst the progeny of the neuroblast. Comparisons of cell morphology, immunoreactivity (horseradish peroxidase, repo, Prospero), location in lineages and spindle orientation have allowed us to distinguish the proliferative cells in an array from neuroblasts, ganglion mother cells, neuronal progeny and glia. Our data are consistent with the proliferative cells being secondary (amplifying) progenitors and originating from a specific subtype of ganglion mother cell. We propose a model of the way that neuroblasts, ganglion mother cells and secondary progenitors together produce the large cell numbers found in central complex lineages.
引用
收藏
页码:259 / 277
页数:19
相关论文
共 76 条
[1]   Essential roles of Drosophila inner centromere protein (INCENP) and aurora B in histone H3 phosphorylation, metaphase chromosome alignment, kinetochore disjunction, and chromosome segregation [J].
Adams, RR ;
Maiato, H ;
Earnshaw, WC ;
Carmena, M .
JOURNAL OF CELL BIOLOGY, 2001, 153 (04) :865-879
[2]  
[Anonymous], 1965, STRUCTURE FUNCTION N
[3]  
[Anonymous], 1976, ATLAS INSECT BRAIN, DOI DOI 10.1007/978-3-642-66179-2
[4]  
BATE CM, 1976, J EMBRYOL EXP MORPH, V35, P107
[5]   A pulse of the Drosophila Hox protein abdominal-A schedules the end of neural proliferation via neuroblast apoptosis [J].
Bello, BC ;
Hirth, F ;
Gould, AP .
NEURON, 2003, 37 (02) :209-219
[6]   Amplification of neural stem cell proliferation by intermediate progenitor cells in Drosophila brain development [J].
Bello, Bruno C. ;
Izergina, Natalya ;
Caussinus, Emmanuel ;
Reichert, Heinrich .
NEURAL DEVELOPMENT, 2008, 3 (1)
[7]  
BENTLEY D, 1979, J EMBRYOL EXP MORPH, V54, P47
[8]   POSTEMBRYONIC NEUROGENESIS IN THE CNS OF THE TOBACCO HORNWORM, MANDUCA-SEXTA .1. NEUROBLAST ARRAYS AND THE FATE OF THEIR PROGENY DURING METAMORPHOSIS [J].
BOOKER, R ;
TRUMAN, JW .
JOURNAL OF COMPARATIVE NEUROLOGY, 1987, 255 (04) :548-559
[9]   Identification of Drosophila type II neuroblast lineages containing transit amplifying ganglion mother cells [J].
Boone, Jason Q. ;
Doe, Chris Q. .
DEVELOPMENTAL NEUROBIOLOGY, 2008, 68 (09) :1185-1195
[10]   The tumor suppressors brat and numb regulate transit-amplifying neuroblast lineages in Drosophila [J].
Bowman, Sarah K. ;
Rolland, Vivien ;
Betschinger, Joerg ;
Kinsey, Kaolin A. ;
Emery, Gregory ;
Knoblich, Juergen A. .
DEVELOPMENTAL CELL, 2008, 14 (04) :535-546