In Vivo Clonal Analysis Reveals Self-Renewing and Multipotent Adult Neural Stem Cell Characteristics

被引:684
作者
Bonaguidi, Michael A. [1 ,2 ]
Wheeler, Michael A. [1 ]
Shapiro, Jason S. [1 ]
Stadel, Ryan P. [1 ,3 ]
Sun, Gerald J. [1 ,4 ]
Ming, Guo-li [1 ,2 ,4 ]
Song, Hongjun [1 ,2 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Human Genet Predoctoral Training Program, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA
关键词
RADIAL GLIAL-CELLS; HIPPOCAMPAL NEUROGENESIS; SUBVENTRICULAR ZONE; NEURONS; ASTROCYTES; LINEAGE; PTEN; QUIESCENT; DIFFERENTIATION; PROGENITOR;
D O I
10.1016/j.cell.2011.05.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1142 / 1155
页数:14
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