MAZ mediates the cross-talk between CT-1 and NOTCH1 signaling during gliogenesis.
نویسندگان
چکیده
Neurons and glia cells are differentiated from neural stem/progenitor cells (NSCs/NPCs) during brain development. Concomitant activation of JAK/STAT and NOTCH1 signaling is required for gliogenesis, a process to generate glia cells to ensure proper brain functions. NOTCH1 signaling is down-regulated during neurogenesis and up-regulated during gliogenesis. However, the underlying mechanism remains elusive. We report here that cardiotrophin-1 (CT-1) activates NOTCH1 signaling through the up-regulation of ADAM10, a rate-limiting factor of NOTCH1 signaling activation. We found that a transcriptional factor, Myc-associated zinc finger protein (MAZ), plays an important role in ADAM10 transcription in response to CT-1 in NPCs. MAZ knockdown inhibits CT-1 stimulated gliogenesis and it can be rescued by over-expressing human NICD. Our results provide a link between NOTCH1 activation and neuronal secreted CT-1, suggesting that CT-1 plays an important role in ensuring the coordinated activation of NOTCH1 signaling during gliogenesis.
منابع مشابه
Corrigendum: MAZ mediates the cross-talk between CT-1 and NOTCH1 signaling during gliogenesis
In this Article, the legend of Figure 1 contains a typographical error. " Two downstream effectors of NOTCH1 pathway, Hes1 & Hes5 were examined by qRT-PCR after CT-1 stimulation for 24 hrs in NIH3T3 cells (E) or 48 hrs in NPCs (F). " should read: " Two downstream effectors of NOTCH1 pathway, Hes1 & Hes5 were examined by qRT-PCR after CT-1 stimulation for 24 hrs in NIH3T3 cells (F) or 48 hrs in ...
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عنوان ژورنال:
- Scientific reports
دوره 6 شماره
صفحات -
تاریخ انتشار 2016