Neural stem/progenitor cell (NSPC) multipotency is highly regulated so that specific neural networks form during development. NSPCs cannot respond to gliogenic signals without acquiring gliogenic competence and decreasing their neurogenic competence as development proceeds. Coup-tfI and Coup-tfII are triggers of these temporal NSPC competence changes. However, the downstream effectors of Coup-tfs that mediate the neurogenic-to-gliogenic competence transition remain unknown. Here, we identified the microRNA-17/106 (miR-17/106)-p38 axis as a critical regulator of this transition. Overexpression of miR-17 inhibited the acquisition of gliogenic competence and forced stage-progressed NSPCs to regain neurogenic competence without altering the methylation status of a glial gene promoter. We also identified Mapk14 (also known as p38) as a target of miR-17/106 and found that Mapk14 inhibition restored neurogenic competence after the neurogenic phase. These results demonstrate that the miR-17/106-p38 axis is a key regulator of the neurogenic-to-gliogenic NSPC competence transition and that manipulation of this axis permits bidirectional control of NSPC multipotency.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3910627PMC
http://dx.doi.org/10.1073/pnas.1315567111DOI Listing

Publication Analysis

Top Keywords

mir-17/106-p38 axis
12
neurogenic competence
12
axis key
8
key regulator
8
regulator neurogenic-to-gliogenic
8
neural stem/progenitor
8
nspc multipotency
8
competence
8
gliogenic competence
8
nspc competence
8

Similar Publications

The miR-17/106-p38 axis is a key regulator of the neurogenic-to-gliogenic transition in developing neural stem/progenitor cells.

Proc Natl Acad Sci U S A

January 2014

Laboratory for Stem Cell Competency, Research Center for Allergy and Immunology (RCAI), RIKEN Center for Integrative Medical Sciences (IMS-RCAI), Suehirocho, Tsurumi-ku, Yokohama 230-0045, Japan.

Neural stem/progenitor cell (NSPC) multipotency is highly regulated so that specific neural networks form during development. NSPCs cannot respond to gliogenic signals without acquiring gliogenic competence and decreasing their neurogenic competence as development proceeds. Coup-tfI and Coup-tfII are triggers of these temporal NSPC competence changes.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!