rax, hes1, and notch1 promote the formation of Muller glia by postnatal retinal progenitor cells

被引:408
作者
Furukawa, T
Mukherjee, S
Bao, ZZ
Morrow, EM
Cepko, CL [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[3] Univ Texas, SW Med Ctr, Ctr Dev Biol, Dallas, TX 75390 USA
关键词
D O I
10.1016/S0896-6273(00)81171-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We are interested in the mechanisms of glial cell development in the vertebrate central nervous system. We have identified genes that can direct the formation of glia in the retina, rax, a homeobox gene, Hes1, a basic helix-loop-helix gene, and notch1, a transmembrane receptor gene, are expressed in retinal progenitor cells, downregulated in differentiated neurons, and expressed in Muller glia. Retroviral transduction of any of these genes resulted in expression of glial markers. In contrast, misexpression of a dominant-negative Hes1 gene reduced the number of glia. Cotransfection of rax with reporter constructs containing the Hes1 or notch1 regulatory regions led to the upregulation of reporter transcription. These data suggest a regulatory heirarchy that controls the formation of glia at the expense of neurons.
引用
收藏
页码:383 / 394
页数:12
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