Author/Authors :
Hu، نويسنده , , Yi-Yang and Fu، نويسنده , , Luo-An and Li، نويسنده , , San-Zhong and Chen، نويسنده , , Yan and Li، نويسنده , , Jun-Chang and Han، نويسنده , , Jun and Liang، نويسنده , , Liang and Li، نويسنده , , Liang and Ji، نويسنده , , Chen-Chen and Zheng، نويسنده , , Min-Hua and Han، نويسنده , , Hua، نويسنده ,
Abstract :
Hypoxia contributes to GSC expansion principally through Hif-1α and Hif-2α, but how these two factors work together has not been completely understood. We show that hypoxia promoted proliferation, self-renewal and inhibited the conversion of GSCs into INP-like cells through activating Notch signaling. Further data suggested that Hif-2α interacted with NICD and repressed the activity of Notch signaling, in contrast to the role of Hif-1α in Notch signaling. Together, our findings suggest that Hif-1α and Hif-2α competitively bind to NICD and dynamically regulate the activation of Notch signaling in GSCs likely depending on different oxygen tensions, providing improved therapeutic opportunities for malignant gliomas.
Keywords :
Glioma stem cells , Hypoxia , HIF-2? , HIF-1? , Notch