Sonic hedgehog controls stem cell behavior in the postnatal and adult brain

被引:472
作者
Palma, V
Lim, DA
Dahmane, N
Sánchez, P
Brlonne, TC
Herzberg, CD
Gitton, Y
Carleton, A
Alvarez-Buylla, A
Altaba, ARI
机构
[1] NYU, Sch Med, Skirball Inst, New York, NY 10016 USA
[2] Univ Calif San Francisco, San Francisco, CA 94143 USA
[3] Univ Geneva, Sch Med, CH-1211 Geneva 4, Switzerland
[4] Ecole Polytech Fed Lausanne, Brain & Mind Inst, CH-1015 Lausanne, Switzerland
来源
DEVELOPMENT | 2005年 / 132卷 / 02期
关键词
mouse; stem cell; brain; hedgehog; Gli; subventricular zone;
D O I
10.1242/dev.01567
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sonic hedgehog (Shh) signaling controls many; aspects of ontogeny, orchestrating congruent growth and patterning. During brain development, Shh regulates early ventral patterning while later on it is critical for the regulation of precursor proliferation in the dorsal brain, namely in the neocortex, tectum and cerebellum. We have recently shown that Shh also controls the behavior of cells with stem cell properties in the mouse embryonic neocortex, and additional studies have implicated it in the control of cell proliferation in the adult ventral forebrain and in the hippocampus. However, it remains unclear whether it regulates adult stem cell lineages in an equivalent manner. Similarly, it is not known which cells respond to Shh signaling in stem cell niches. Here we demonstrate that Shh is required for cell proliferation in the mouse forebrain's subventricular zone (SVZ) stem cell niche and for the production of new olfactory interneurons in vivo. We identify two populations of Gli1(+) Shh signaling responding cells: GFAP(+) SVZ stem cells and GFAP(-) precursors. Consistently, We show that Shh regulates the self-renewal of neurosphere-forming stem cells and that it modulates proliferation of SVZ lineages by acting as a mitogen in cooperation with epidermal growth factor (EGF). Together, our data demonstrate a critical and conserved role of Shh signaling in the regulation of stem cell lineages in the adult mammalian brain, highlight the subventricular stem cell astrocytes and their more abundant derived precursors as in vivo targets of Shh signaling, and demonstrate the requirement for Shh signaling in postnatal and adult neurogenesis.
引用
收藏
页码:335 / 344
页数:10
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