Molecular control of cell type diversity in the developing spinal cord

被引:0
|
作者
Yamada, T [1 ]
Karunaratne, A
Hargrave, M
机构
[1] Univ Queensland, Ctr Cellular & Mol Biol, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Dept Biochem, Brisbane, Qld 4072, Australia
关键词
bone morphogenic protein; cell patterning; interneuron; LIM-homeodomain; motor neuron; Pax genes; Sonic hedgehog; spinal cord development; transcription factor; transforming growth factor-beta;
D O I
10.1046/j.1440-1681.1999.03107.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1, During embryonic development, a diverse array of neurons and glia are generated at specific positions along the dorsoventral and rostro-caudal axes of the spinal cord from a common pool of precursor cells. 2. This cell type diversity can be distinguished by the spatially and temporally coordinated expression of several transcription factors that are also linked to cell type specification at a very early stage of spinal cord development. 3, Recent studies have started to uncover that the generation of cell type diversity in the developing spinal cord. Moreover, distinct cell types in the spinal cord appear to be determined by the spatially and temporally coordinated expression of transcription factors. 4. The expression of these factors also appears to be controlled by gradients of factors expressed by ventral and dorsal midline cells, namely Sonic hedgehog and members of the transforming growth factor-beta family. 5, Changes in the competence of precursor cells and local cell interactions may also play important roles in cell type specification within the developing spinal cord.
引用
收藏
页码:741 / 745
页数:5
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