Generation of Multiple Classes of V0 Neurons in Zebrafish Spinal Cord: Progenitor Heterogeneity and Temporal Control of Neuronal Diversity

被引:109
作者
Satou, Chie [1 ,2 ]
Kimura, Yukiko [1 ]
Higashijima, Shin-ichi [1 ,2 ]
机构
[1] Natl Inst Physiol Sci, Natl Inst Nat Sci, Okazaki Inst Integrat Biosci, Okazaki, Aichi 4448787, Japan
[2] Grad Univ Adv Studies, Okazaki, Aichi 4448787, Japan
关键词
TOL2 TRANSPOSABLE ELEMENT; FUNCTIONAL GROUND PLAN; CENTRAL-NERVOUS-SYSTEM; LARVAL ZEBRAFISH; TRANSGENIC ZEBRAFISH; LOCOMOTOR-ACTIVITY; VERTEBRATE RETINA; CEREBRAL-CORTEX; CELL FATES; INTERNEURONS;
D O I
10.1523/JNEUROSCI.5500-11.2012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The developing spinal cord is subdivided into distinct progenitor domains, each of which gives rise to different types of neurons. However, the developmental mechanisms responsible for generating neuronal diversity within a domain are not well understood. Here, we have studied zebrafish V0 neurons, those that derive from the p0 progenitor domain, to address this question. We find that all V0 neurons have commissural axons, but they can be divided into excitatory and inhibitory classes. V0 excitatory neurons (V0-e) can be further categorized into three groups based on their axonal trajectories; V0-eA (ascending), V0-eB (bifurcating), and V0-eD (descending) neurons. By using time-lapse imaging of p0 progenitors and their progeny, we show that inhibitory and excitatory neurons are produced from different progenitors. We also demonstrate that V0-eA neurons are produced from distinct progenitors, while V0-eB and V0-eD neurons are produced from common progenitors. We then use birth-date analysis to reveal that V0-eA, V0-eB, and V0-eD neurons arise in this order. By perturbing Notch signaling and accelerating neuronal differentiation, we predictably alter the generation of early born V0-e neurons at the expense of later born ones. These results suggest that multiple types of V0 neurons are produced by two distinct mechanisms; from heterogeneous p0 progenitors and from the same p0 progenitor, but in a time-dependent manner.
引用
收藏
页码:1771 / 1783
页数:13
相关论文
共 46 条
[1]   Temporally regulated asymmetric neurogenesis causes left-right difference in the zebrafish habenular structures [J].
Aizawa, Hidenori ;
Goto, Midori ;
Sato, Tomomi ;
Okamoto, Hitoshi .
DEVELOPMENTAL CELL, 2007, 12 (01) :87-98
[2]   Postnatal phenotype and localization of spinal cord V1 derived interneurons [J].
Alvarez, FJ ;
Jonas, PC ;
Sapir, T ;
Hartley, R ;
Berrocal, MC ;
Geiman, EJ ;
Todd, AJ ;
Goulding, M .
JOURNAL OF COMPARATIVE NEUROLOGY, 2005, 493 (02) :177-192
[3]   GFAP transgenic zebrafish [J].
Bernardos, Rebecca L. ;
Raymond, Pamela A. .
GENE EXPRESSION PATTERNS, 2006, 6 (08) :1007-1013
[4]   The embryonic central nervous system lineages of Drosophila melanogaster .1. Neuroblast lineages derived from the ventral half of the neuroectoderm [J].
Bossing, T ;
Udolph, G ;
Doe, CQ ;
Technau, GM .
DEVELOPMENTAL BIOLOGY, 1996, 179 (01) :41-64
[5]   Hindbrain interneurons and axon guidance signaling critical for breathing [J].
Bouvier, Julien ;
Thoby-Brisson, Muriel ;
Renier, Nicolas ;
Dubreuil, Veronique ;
Ericson, Johan ;
Champagnat, Jean ;
Pierani, Alessandra ;
Chedotal, Alain ;
Fortin, Gilles .
NATURE NEUROSCIENCE, 2010, 13 (09) :1066-U55
[6]   Ascl1 expression defines a subpopulation of lineage-restricted progenitors in the mammalian retina [J].
Brzezinski, Joseph A. ;
Kim, Euiseok J. ;
Johnson, Jane E. ;
Reh, Thomas A. .
DEVELOPMENT, 2011, 138 (16) :3519-3531
[7]   Lineage in the vertebrate retina [J].
Cayouette, Michel ;
Poggi, Lucia ;
Harris, William A. .
TRENDS IN NEUROSCIENCES, 2006, 29 (10) :563-570
[8]   Cell fate determination in the vertebrate retina [J].
Cepko, CL ;
Austin, CP ;
Yang, XJ ;
Alexiades, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) :589-595
[9]   The roles of intrinsic and extrinsic cues and bHLH genes in the determination of retinal cell fates [J].
Cepko, CL .
CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (01) :37-46
[10]   Tlx3 and Tlx1 are post-mitotic selector genes determining glutamatergic over GABAergic cell fates [J].
Cheng, LP ;
Arata, A ;
Mizuguchi, R ;
Qian, Y ;
Karunaratne, A ;
Gray, PA ;
Arata, S ;
Shirasawa, S ;
Bouchard, M ;
Luo, P ;
Chen, CL ;
Busslinger, M ;
Goulding, M ;
Onimaru, H ;
Ma, QF .
NATURE NEUROSCIENCE, 2004, 7 (05) :510-517