Biozentrum, University of Basel, Basel, Switzerland.
Department of Neurology, Columbia University, New York, NY, USA.
Science. 2021 Jun 11;372(6547):1205-1209. doi: 10.1126/science.abg8467.
Quiescent neural stem cells (NSCs) in the adult mouse ventricular-subventricular zone (V-SVZ) undergo activation to generate neurons and some glia. Here we show that platelet-derived growth factor receptor beta (PDGFRβ) is expressed by adult V-SVZ NSCs that generate olfactory bulb interneurons and glia. Selective deletion of PDGFRβ in adult V-SVZ NSCs leads to their release from quiescence, uncovering gliogenic domains for different glial cell types. These domains are also recruited upon injury. We identify an intraventricular oligodendrocyte progenitor derived from NSCs inside the brain ventricles that contacts supraependymal axons. Together, our findings reveal that the adult V-SVZ contains spatial domains for gliogenesis, in addition to those for neurogenesis. These gliogenic NSC domains tend to be quiescent under homeostasis and may contribute to brain plasticity.
静息性神经干细胞(NSC)在成年小鼠脑室下区(V-SVZ)中被激活,生成神经元和一些胶质细胞。本文中,我们发现血小板衍生生长因子受体β(PDGFRβ)在成年 V-SVZ NSC 中表达,这些细胞生成嗅球中间神经元和胶质细胞。选择性敲除成年 V-SVZ NSC 中的 PDGFRβ 会导致其从静息中释放出来,揭示了不同胶质细胞类型的神经发生领域。这些区域也在损伤时被招募。我们鉴定出一种脑室间少突胶质前体细胞,它起源于脑室内的 NSC,可以接触到室管膜上的轴突。总之,我们的发现表明,成年 V-SVZ 除了具有神经发生区域外,还包含胶质发生区域。这些胶质发生的 NSC 区域在稳态下往往处于静息状态,可能有助于大脑的可塑性。