Puverel Sandrine, Nakatani Hiroko, Parras Carlos, Soussi-Yanicostas Nadia
Institut National de la Santé et de la Recherche Médicale Equipe Avenir, Zebrafish Neurogenesis, IFR70, Hôpital de la Pitié-Salpêtrière, 75651 Paris, France.
J Comp Neurol. 2009 Jan 10;512(2):232-42. doi: 10.1002/cne.21888.
The adult subventricular zone (SVZ) contains progenitors cells, which continually give rise to new neurons that migrate along the rostral migratory stream (RMS) to the olfactory bulbs (OB). Prokineticin receptor 2 (ProKR2) is a G-protein-coupled receptor that plays an essential role in this migration process. However, the identity of the prokr2-expressing cells has not yet been clearly established. Here, we have characterized in detail the identity of the prokr2-expressing cells in the SVZ/RMS/OB pathway in adult mice. In the SVZ, accumulation of prokr2 transcripts was detected in almost all migrating neuroblasts or type A cells as well as in a large population of their precursors, the rapidly dividing type C cells. Moreover, we observed that, in dissociated SVZ cells from Mash1::GFP postnatal mice, ProKR2 protein is also present in type C and type A cells. We found that, along the RMS and in the OB, prokr2 expression was restricted to migrating type A cells and was absent in astrocytes. Finally, we observed a highly marked decrease of prokr2 expression in Mash1-/- mutant mice, suggesting that this transcription factor directly or indirectly regulates prokr2 expression. Although the expression of ProKR2 in migrating type A cells is in good agreement with the essential role played by this receptor during this migration process, its expression in a large population of their progenitors suggests an additional function for ProKR2, providing novel insights into the role of ProKR2/ProK2 signalling in adult neurogenesis.
成体脑室下区(SVZ)含有祖细胞,这些祖细胞持续产生新的神经元,这些神经元沿着吻侧迁移流(RMS)迁移至嗅球(OB)。促动力蛋白受体2(ProKR2)是一种G蛋白偶联受体,在这一迁移过程中发挥着重要作用。然而,表达prokr2的细胞的身份尚未明确确定。在这里,我们详细鉴定了成年小鼠SVZ/RMS/OB通路中表达prokr2的细胞的身份。在SVZ中,在几乎所有迁移的神经母细胞或A型细胞以及大量其前体——快速分裂的C型细胞中都检测到了prokr2转录本的积累。此外,我们观察到,在来自出生后Mash1::GFP小鼠的解离的SVZ细胞中,ProKR2蛋白也存在于C型和A型细胞中。我们发现,沿着RMS以及在OB中,prokr2的表达仅限于迁移的A型细胞,星形胶质细胞中不存在。最后,我们观察到Mash1-/-突变小鼠中prokr2表达显著降低,这表明该转录因子直接或间接调节prokr2的表达。尽管ProKR2在迁移的A型细胞中的表达与该受体在这一迁移过程中所起的重要作用一致,但其在大量其祖细胞中的表达表明ProKR2具有额外的功能,为ProKR2/ProK2信号在成体神经发生中的作用提供了新的见解。