Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Cell. 2011 Jun 24;145(7):1142-55. doi: 10.1016/j.cell.2011.05.024. Epub 2011 Jun 16.
Neurogenesis and gliogenesis continue in discrete regions of the adult mammalian brain. A fundamental question remains whether cell genesis occurs from distinct lineage-restricted progenitors or from self-renewing and multipotent neural stem cells in the adult brain. Here, we developed a genetic marking strategy for lineage tracing of individual, quiescent, and nestin-expressing radial glia-like (RGL) precursors in the adult mouse dentate gyrus. Clonal analysis identified multiple modes of RGL activation, including asymmetric and symmetric self-renewal. Long-term lineage tracing in vivo revealed a significant percentage of clones that contained RGL(s), neurons, and astrocytes, indicating capacity of individual RGLs for both self-renewal and multilineage differentiation. Furthermore, conditional Pten deletion in RGLs initially promotes their activation and symmetric self-renewal but ultimately leads to terminal astrocytic differentiation and RGL depletion in the adult hippocampus. Our study identifies RGLs as self-renewing and multipotent neural stem cells and provides novel insights into in vivo properties of adult neural stem cells.
神经发生和神经胶质发生在成年哺乳动物大脑的特定区域继续进行。一个基本问题仍然是细胞发生是来自特定谱系限制的祖细胞还是来自成年大脑中的自我更新和多能神经干细胞。在这里,我们开发了一种遗传标记策略,用于追踪成年小鼠齿状回中单个、静止和巢蛋白表达的放射状胶质样(RGL)前体细胞的谱系。克隆分析确定了多种 RGL 激活模式,包括不对称和对称自我更新。体内长期谱系追踪显示,有相当比例的克隆包含 RGL(s)、神经元和星形胶质细胞,表明单个 RGL 具有自我更新和多谱系分化的能力。此外,RGL 中的条件性 Pten 缺失最初促进其激活和对称自我更新,但最终导致成年海马体中终末星形胶质细胞分化和 RGL 耗竭。我们的研究将 RGL 鉴定为自我更新和多能神经干细胞,并为成年神经干细胞的体内特性提供了新的见解。