Invasion of white matter tracts by glioma stem cells is regulated by a NOTCH1–SOX2 positive-feedback loop

Early invasive growth along specific anatomical structures, especially the white matter tract, is regarded as one of the main causes of poor therapeutic outcome of people with gliomas. We show that some glioma stem cells (GSCs) are preferentially located along white matter tracts, which exhibit a de...

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Veröffentlicht in:Nature neuroscience 2019-01, Vol.22 (1), p.91-105
Hauptverfasser: Wang, Jun, Xu, Sen-Lin, Duan, Jiang-Jie, Yi, Liang, Guo, Yu-Feng, Shi, Yu, Li, Lin, Yang, Ze-Yu, Liao, Xue-Mei, Cai, Jiao, Zhang, Yan-Qi, Xiao, Hua-Liang, Yin, Li, Wu, Hao, Zhang, Jing-Na, Lv, Sheng-Qing, Yang, Qing-Kai, Yang, Xiao-Jun, Jiang, Tao, Zhang, Xia, Bian, Xiu-Wu, Yu, Shi-Cang
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Sprache:eng
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Zusammenfassung:Early invasive growth along specific anatomical structures, especially the white matter tract, is regarded as one of the main causes of poor therapeutic outcome of people with gliomas. We show that some glioma stem cells (GSCs) are preferentially located along white matter tracts, which exhibit a demyelinated phenotype, at the invasive frontier of glioma tissues. These GSCs are CD133 + Notch1 + , whereas the nerve fibers express the Notch ligand Jagged1. The Notch-induced transcription factor Sox9 promotes the transcription of SOX2 and the methylation level of the NOTCH1 promoter is attenuated by the upregulation of SOX2 to reinforce NOTCH1 expression in GSCs. This positive-feedback loop in a cohort of glioma subjects is correlated with a poor prognosis. Inhibition of Notch signaling attenuates the white-matter-tract tropism of GSCs. These findings provide evidence indicating that the NOTCH1 - SOX2 positive-feedback loop controls GSC invasion along white matter tracts. CD133 and Notch1 double-positive GSCs were preferentially located along Jagged1-expressing white matter tracts, which exhibited a demyelinated phenotype. The NOTCH1 – SOX9 – SOX2 positive-feedback loop controls GSC invasion along white matter tracts.
ISSN:1097-6256
1546-1726
DOI:10.1038/s41593-018-0285-z