A Dlx2-and Pax6-dependent transcriptional code for periglomerular neuron specification in the adult olfactory bulb

被引:162
作者
Brill, Monika S. [1 ,2 ,3 ]
Snapyan, Marina [4 ]
Wohlfrom, Hilde [1 ,2 ,3 ]
Ninkovic, Jovica [2 ,3 ]
Jawerka, Melanie [1 ,2 ,3 ]
Mastick, Grant S. [5 ]
Ashery-Padan, Ruth [6 ]
Saghatelyan, Armen [4 ]
Berninger, Benedikt [1 ,2 ,3 ]
Goetz, Magdalena [1 ,2 ,3 ]
机构
[1] Univ Munich, Inst Physiol, Dept Physiol Gen, D-80336 Munich, Germany
[2] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Inst Stem Cell Res, D-85764 Neuherberg, Germany
[3] Munich Ctr Integrated Prot Sci, D-81377 Munich, Germany
[4] Univ Laval Robert Giffard, Ctr Rech, Unite Neurobiol Cellulaire, Quebec City, PQ G1J 2G3, Canada
[5] Univ Nevada, Dept Biol, Reno, NV 89557 USA
[6] Tel Aviv Univ, Sackler Fac Med, Dept Human Mol Genet & Biochem, IL-69978 Tel Aviv, Israel
关键词
neurogenesis; subependymal zone; olfactory bulb; transcription factor; tyrosine hydroxylase; stem cell;
D O I
10.1523/JNEUROSCI.0700-08.2008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Distinct olfactory bulb (OB) interneurons are thought to become specified depending on from which of the different subregions lining the lateral ventricle wall they originate, but the role of region-specific transcription factors (TFs) in the generation of OB interneurons diversity is still poorly understood. Despite the crucial roles of the Dlx family of TFs for patterning and neurogenesis in the ventral telencephalon during embryonic development, their role in adult neurogenesis has not yet been addressed. Here we show that in the adult brain, Dlx 1 and Dlx2 are expressed in progenitors of the lateral but not the dorsal subependymal zone (SEZ), thus exhibiting a striking regional specificity. Using retroviral vectors to examine the function of Dlx2 in a cell-autonomous manner, we demonstrate that this TF is necessary for neurogenesis of virtually all OB interneurons arising from the lateral SEZ. Beyond its function in generic neurogenesis, Dlx2 also plays a crucial role in neuronal subtype specification in the OB, promoting specification of adult-born periglomerular neurons (PGNs) toward a dopaminergic fate. Strikingly, Dlx2 requires interaction with Pax6, because Pax6 deletion blocks Dlx2-mediated PGN specification. Thus, Dlx2 wields a dual function by first instructing generic neurogenesis from adult precursors and subsequently specifying PGN subtypes in conjunction with Pax6.
引用
收藏
页码:6439 / 6452
页数:14
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