Activation of a neural stem cell transcriptional program in parenchymal astrocytes

  1. Jens P Magnusson
  2. Margherita Zamboni
  3. Giuseppe Santopolo
  4. Jeff E Mold
  5. Mauricio Barrientos-Somarribas
  6. Carlos Talavera-Lopez
  7. Björn Andersson
  8. Jonas Frisén  Is a corresponding author
  1. Stanford University, United States
  2. Karolinska Institutet, Sweden
  3. Francis Crick Institute, United Kingdom
  4. Karolinska Institute, Sweden

Abstract

Adult neural stem cells, located in discrete brain regions, generate new neurons throughout life. These stem cells are specialized astrocytes, but astrocytes in other brain regions do not generate neurons under physiological conditions. After stroke, however, striatal astrocytes undergo neurogenesis in mice, triggered by decreased Notch signaling. We used single-cell RNA sequencing to characterize neurogenesis by Notch-depleted striatal astrocytes in vivo. Striatal astrocytes were located upstream of neural stem cells in the neuronal lineage. As astrocytes initiated neurogenesis, they became transcriptionally very similar to subventricular zone stem cells, progressing through a near-identical neurogenic program. Surprisingly, in the non-neurogenic cortex, Notch-depleted astrocytes also initiated neurogenesis. Yet, these cortical astrocytes, and many striatal ones, stalled before entering transit-amplifying divisions. Infusion of epidermal growth factor enabled stalled striatal astrocytes to resume neurogenesis. We conclude that parenchymal astrocytes are latent neural stem cells and that targeted interventions can guide them through their neuronal differentiation.

Data availability

The Cx30-CreER dataset (fastq files and processed expression matrix) has been deposited in ArrayExpress (accession E-MTAB-9268). The AAV-Cre dataset has been deposited in the Gene Expression Omnibus (GEO; accession GSE153916).SmartSeq2 dataset (ArrayExpress)http://www.ebi.ac.uk/arrayexpress/help/how_to_search_private_data.htmlUsername: Reviewer_E-MTAB-9268Password: hqhgiiqx10X dataset (GEO)To review GEO accession GSE153916:Go to https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE153916Enter token mzoxeoigpranfub into the box

The following data sets were generated
The following previously published data sets were used

Article and author information

Author details

  1. Jens P Magnusson

    Bioengineering Department, Stanford University, Stanford, United States
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-3928-8959
  2. Margherita Zamboni

    Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden
    Competing interests
    The authors declare that no competing interests exist.
  3. Giuseppe Santopolo

    Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden
    Competing interests
    The authors declare that no competing interests exist.
  4. Jeff E Mold

    Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden
    Competing interests
    The authors declare that no competing interests exist.
  5. Mauricio Barrientos-Somarribas

    Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden
    Competing interests
    The authors declare that no competing interests exist.
  6. Carlos Talavera-Lopez

    Francis Crick Institute, Francis Crick Institute, London, United Kingdom
    Competing interests
    The authors declare that no competing interests exist.
  7. Björn Andersson

    Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden
    Competing interests
    The authors declare that no competing interests exist.
  8. Jonas Frisén

    Cell and Molecular Biology, Karolinska Institute, Stockholm, Sweden
    For correspondence
    jonas.frisen@ki.se
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-5819-458X

Funding

Svenska Forskningsrådet Formas

  • Jonas Frisén

Cancerfonden

  • Jonas Frisén

Stiftelsen för Strategisk Forskning

  • Jonas Frisén

H2020 European Research Council

  • Jonas Frisén

Knut och Alice Wallenbergs Stiftelse

  • Jonas Frisén

Torsten Söderbergs Stiftelse

  • Jonas Frisén

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Ethics

Animal experimentation: All animal experimental procedures were approved by the Stockholms Norra Djurförsöksetiska Nämnd (Permit reference numbers N571-11 and N155-16)

Copyright

© 2020, Magnusson et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 7,556
    views
  • 866
    downloads
  • 64
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Jens P Magnusson
  2. Margherita Zamboni
  3. Giuseppe Santopolo
  4. Jeff E Mold
  5. Mauricio Barrientos-Somarribas
  6. Carlos Talavera-Lopez
  7. Björn Andersson
  8. Jonas Frisén
(2020)
Activation of a neural stem cell transcriptional program in parenchymal astrocytes
eLife 9:e59733.
https://doi.org/10.7554/eLife.59733

Share this article

https://doi.org/10.7554/eLife.59733

Further reading

    1. Neuroscience
    Jacob A Miller
    Insight

    When navigating environments with changing rules, human brain circuits flexibly adapt how and where we retain information to help us achieve our immediate goals.

    1. Neuroscience
    Franziska Auer, Katherine Nardone ... David Schoppik
    Research Article

    Cerebellar dysfunction leads to postural instability. Recent work in freely moving rodents has transformed investigations of cerebellar contributions to posture. However, the combined complexity of terrestrial locomotion and the rodent cerebellum motivate new approaches to perturb cerebellar function in simpler vertebrates. Here, we adapted a validated chemogenetic tool (TRPV1/capsaicin) to describe the role of Purkinje cells — the output neurons of the cerebellar cortex — as larval zebrafish swam freely in depth. We achieved both bidirectional control (activation and ablation) of Purkinje cells while performing quantitative high-throughput assessment of posture and locomotion. Activation modified postural control in the pitch (nose-up/nose-down) axis. Similarly, ablations disrupted pitch-axis posture and fin-body coordination responsible for climbs. Postural disruption was more widespread in older larvae, offering a window into emergent roles for the developing cerebellum in the control of posture. Finally, we found that activity in Purkinje cells could individually and collectively encode tilt direction, a key feature of postural control neurons. Our findings delineate an expected role for the cerebellum in postural control and vestibular sensation in larval zebrafish, establishing the validity of TRPV1/capsaicin-mediated perturbations in a simple, genetically tractable vertebrate. Moreover, by comparing the contributions of Purkinje cell ablations to posture in time, we uncover signatures of emerging cerebellar control of posture across early development. This work takes a major step towards understanding an ancestral role of the cerebellum in regulating postural maturation.