Neuron-glia interaction through Serotonin-BDNF-NGFR axis enables regenerative neurogenesis in Alzheimer’s model of adult zebrafish brain

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Prabesh Bhattarai - , Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) (Autor:in)
  • Mehmet Ilyas Cosacak - , Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) (Autor:in)
  • Violeta Mashkaryan - , Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) (Autor:in)
  • Sevgican Demir - , Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) (Autor:in)
  • Stanislava Dimitrova Popova - , Center for Regenerative Therapies Dresden (CRTD), Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) (Autor:in)
  • Nambirajan Govindarajan - , Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) (Autor:in)
  • Kerstin Brandt - , Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) (Autor:in)
  • Yixin Zhang - , Professur für Biomolekulare Interaktionen (Autor:in)
  • Weipang Chang - , Karolinska Institutet (Autor:in)
  • Konstantinos Ampatzis - , Karolinska Institutet (Autor:in)
  • Caghan Kizil - , Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) (Autor:in)

Abstract

It was recently suggested that supplying the brain with new neurons could counteract Alzheimer’s disease (AD). This provocative idea requires further testing in experimental models in which the molecular basis of disease-induced neuronal regeneration could be investigated. We previously found that zebrafish stimulates neural stem cell (NSC) plasticity and neurogenesis in AD and could help to understand the mechanisms to be harnessed for developing new neurons in diseased mammalian brains. Here, by performing single-cell transcriptomics, we found that amyloid toxicity-induced interleukin-4 (IL4) promotes NSC proliferation and neurogenesis by suppressing the tryptophan metabolism and reducing the production of serotonin. NSC proliferation was suppressed by serotonin via down-regulation of brain-derived neurotrophic factor (BDNF)-expression in serotonin-responsive periventricular neurons. BDNF enhances NSC plasticity and neurogenesis via nerve growth factor receptor A (NGFRA)/ nuclear factor’kappa-light-chain-enhancer’ of activated B-cells (NFkB) signaling in zebrafish but not in rodents. Collectively, our results suggest a complex neuron-glia interaction that regulates regenerative neurogenesis after AD conditions in zebrafish.

Details

OriginalspracheEnglisch
Aufsatznummere3000585
FachzeitschriftPLoS biology
Jahrgang18
Ausgabenummer1
PublikationsstatusVeröffentlicht - 6 Jan. 2020
Peer-Review-StatusJa

Externe IDs

Scopus 85078512643
PubMed 31905199