Retinal ganglion cell-derived sonic hedgehog signaling is required for optic disc and stalk neuroepithelial cell development

被引:111
作者
Dakubo, GD
Wang, YP
Mazerolle, C
Campsall, K
McMahon, AP
Wallace, VA
机构
[1] Ottawa Hlth Res Inst, Program Mol Med, Ottawa, ON K1H 8L6, Canada
[2] Harvard Univ, Biolabs, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[3] Univ Ottawa, Inst Eye, Ctr Neuromuscular Dis, Ottawa, ON K1H 8M5, Canada
[4] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON K1H 8M5, Canada
来源
DEVELOPMENT | 2003年 / 130卷 / 13期
关键词
retinal ganglion cells; Shh; Ihh; Pax2; optic disc/stalk; neuroepithelial cells; astrocyte precursor cells; development; mouse;
D O I
10.1242/dev.00515
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The development of optic stalk neuroepithelial cells depends on Hedgehog (Hh) signaling, yet the source(s) of Hh protein in the optic stalk is unknown. We provide genetic evidence that sonic hedgehog (Shh) from retinal ganglion cells (RGCs) promotes the development of optic disc and stalk neuroepithelial cells. We demonstrate that RGCs express Shh soon after differentiation, and cells at the optic disc in close proximity to the Shh-expressing RGCs upregulate Hh target genes, which suggests they are responding to RGC-derived Shh signaling. Conditional ablation of Shh in RGCs caused a complete loss of optic disc astrocyte precursor cells, resulting in defective axon guidance in the retina, as well as conversion of the neuroepithelial cells in the optic stalk to pigmented cells. We further show that Shh signaling modulates the size of the Pax2(+) astrocyte precursor cell population at the optic disc in vitro. Together, these data provide a novel insight into the source of Hh that promotes neuroepithelial cell development in the mammalian optic disc and stalk.
引用
收藏
页码:2967 / 2980
页数:14
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