| Literature DB >> 30566853 |
Rossella Di Giaimo1, Tamara Durovic2, Pablo Barquin3, Anita Kociaj2, Tjasa Lepko2, Sven Aschenbroich2, Christopher T Breunig4, Martin Irmler5, Filippo M Cernilogar6, Gunnar Schotta7, Joana S Barbosa8, Dietrich Trümbach9, Emily Violette Baumgart8, Andrea M Neuner4, Johannes Beckers10, Wolfgang Wurst11, Stefan H Stricker4, Jovica Ninkovic12.
Abstract
Zebrafish have a high capacity to replace lost neurons after brain injury. New neurons involved in repair are generated by a specific set of glial cells, known as ependymoglial cells. We analyze changes in the transcriptome of ependymoglial cells and their progeny after injury to infer the molecular pathways governing restorative neurogenesis. We identify the aryl hydrocarbon receptor (AhR) as a regulator of ependymoglia differentiation toward post-mitotic neurons. In vivo imaging shows that high AhR signaling promotes the direct conversion of a specific subset of ependymoglia into post-mitotic neurons, while low AhR signaling promotes ependymoglial proliferation. Interestingly, we observe the inactivation of AhR signaling shortly after injury followed by a return to the basal levels 7 days post injury. Interference with timely AhR regulation after injury leads to aberrant restorative neurogenesis. Taken together, we identify AhR signaling as a crucial regulator of restorative neurogenesis timing in the zebrafish brain.Entities:
Keywords: aryl hydrocarbon receptor; direct conversion; live imaging; neurogenesis; regeneration; zebrafish
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Year: 2018 PMID: 30566853 DOI: 10.1016/j.celrep.2018.11.055
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423