A population of Nestin-expressing progenitors in the cerebellum exhibits increased tumorigenicity

被引:92
作者
Li, Peng [1 ,2 ]
Du, Fang [1 ]
Yuelling, Larra W. [1 ]
Lin, Tiffany [3 ]
Muradimova, Renata E. [1 ]
Tricarico, Rossella [1 ]
Wang, Jun [4 ]
Enikolopov, Grigori [5 ]
Bellacosa, Alfonso [1 ]
Wechsler-Reya, Robert J. [3 ,4 ]
Yang, Zeng-jie [1 ]
机构
[1] Temple Univ Hlth Syst, Fox Chase Canc Ctr, Canc Biol Program, Philadelphia, PA USA
[2] Third Mil Med Univ, Dept Clin Biochem, Southwest Hosp, Chongqing, Peoples R China
[3] Duke Univ, Dept Pharmacol & Canc Biol, Med Ctr, Durham, NC 27710 USA
[4] Sanford Burnham Med Res Inst, Natl Canc Inst Designated Canc Ctr, Tumor Initiat & Maintenance Program, La Jolla, CA USA
[5] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
基金
美国国家卫生研究院;
关键词
NEURAL STEM-CELLS; SONIC HEDGEHOG; MEDULLOBLASTOMA FORMATION; PRECURSOR PROLIFERATION; NEURONAL PROGENITORS; GENOME INSTABILITY; NERVOUS-SYSTEM; RHOMBIC-LIP; MOUSE; NEUROGENESIS;
D O I
10.1038/nn.3553
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
It is generally believed that cerebellar granule neurons originate exclusively from granule neuron precursors (GNPs) in the external germinal layer (EGL). Here we identified a rare population of neuronal progenitors in mouse developing cerebellum that expresses Nestin. Although Nestin is widely considered a marker for multipotent stem cells, these Nestin-expressing progenitors (NEPs) are committed to the granule neuron lineage. Unlike conventional GNPs, which reside in the outer EGL and proliferate extensively, NEPs reside in the deep part of the EGL and are quiescent. Expression profiling revealed that NEPs are distinct from GNPs and, in particular, express markedly reduced levels of genes associated with DNA repair. Consistent with this, upon aberrant activation of Sonic hedgehog (Shh) signaling, NEPs exhibited more severe genomic instability and gave rise to tumors more efficiently than GNPs. These studies revealed a previously unidentified progenitor for cerebellar granule neurons and a cell of origin for medulloblastoma.
引用
收藏
页码:1737 / 1744
页数:8
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