Ascl1 defines sequentially generated lineage-restricted neuronal and oligodendrocyte precursor cells in the spinal cord

被引:131
作者
Battiste, James
Helms, Amy W.
Kim, Euiseok J.
Savage, Trisha K.
Lagace, Diane C.
Mandyam, Chitra D.
Eisch, Amelia J.
Miyoshi, Goichi
Johnson, Jane E. [1 ]
机构
[1] UT SW Med Ctr, Ctr Basic Neurosci, Dallas, TX 75390 USA
[2] UT SW Med Ctr, Dept Psychiat, Dallas, TX 75390 USA
[3] NYU, Sch Med, Smilow Neurosci Program, New York, NY 10016 USA
[4] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
来源
DEVELOPMENT | 2007年 / 134卷 / 02期
关键词
Mash1 (Ascl1); bHLH transcription factor; spinal cord development; in vivo genetic fate mapping; mouse;
D O I
10.1242/dev.02727
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The neural basic helix-loop-helix transcription factor Ascl1 ( previously Mash1) is present in ventricular zone cells in restricted domains throughout the developing nervous system. This study uses genetic fate mapping to define the stage and neural lineages in the developing spinal cord that are derived from Ascl1-expressing cells. We find that Ascl1 is present in progenitors to both neurons and oligodendrocytes, but not astrocytes. Temporal control of the fate-mapping paradigm reveals rapid cell-cycle exit and differentiation of Ascl1-expressing cells. At embryonic day 11, Ascl1 identifies neuronal-restricted precursor cells that become dorsal horn neurons in the superficial laminae. By contrast, at embryonic day 16, Ascl1 identifies oligodendrocyte-restricted precursor cells that distribute throughout the spinal cord. These data demonstrate that sequentially generated Ascl1-expressing progenitors give rise first to dorsal horn interneurons and subsequently to late-born oligodendrocytes. Furthermore, Ascl1-null cells in the spinal cord have a diminished capacity to undergo neuronal differentiation, with a subset of these cells retaining characteristics of immature glial cells.
引用
收藏
页码:285 / 293
页数:9
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