髓母细胞瘤
小脑
生物
音猬因子
干细胞
人口
颗粒细胞
神经科学
祖细胞
内斯汀
病理
神经干细胞
细胞生物学
癌症研究
中枢神经系统
医学
齿状回
环境卫生
信号转导
作者
Maria C. Vladoiu,Ibrahim El-Hamamy,Laura Donovan,Hamza Farooq,Borja Holgado,Vijay Ramaswamy,Stephen C. Mack,John JY Lee,Sachin Kumar,David Przelicki,Antony Michealraj,Kyle Juraschka,Patryk Skowron,Betty Luu,Hiromichi Suzuki,A. Sorana Morrissy,Florence M.G. Cavalli,Livia Garzia,Craig Daniels,Xiaochong Wu
摘要
Summary The study of the origin and development of cerebellar tumours has been hampered by the complexity and heterogeneity of cerebellar cells that change over the course of development. We used single-cell transcriptomics to study >60,000 cells from the developing murine cerebellum, and show that different molecular subgroups of childhood cerebellar tumors mirror the transcription of cells from distinct, temporally restricted cerebellar lineages. Sonic Hedgehog medulloblastoma transcriptionally mirrors the granule cell hierarchy as expected, whereas Group 3 medulloblastoma resemble Nestin +ve stem cells, Group 4 medulloblastomas resemble unipolar brush cells, and PFA/PFB ependymoma and cerebellar pilocytic astrocytoma resemble the prenatal gliogenic progenitor cells. Furthermore, single-cell transcriptomics of human childhood cerebellar tumors demonstrates that many bulk tumors contain a mixed population of cells with divergent differentiation. Our data highlight cerebellar tumors as a disorder of early brain development, and provide a proximate explanation for the peak incidence of cerebellar tumors in early childhood.
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