Apical size and deltaA expression predict adult neural stem cell decisions along lineage progression

Author:

Mancini Laure12ORCID,Guirao Boris3ORCID,Ortica Sara1ORCID,Labusch Miriam12ORCID,Cheysson Felix4ORCID,Bonnet Valentin56ORCID,Phan Minh Son7ORCID,Herbert Sébastien7ORCID,Mahou Pierre8ORCID,Menant Emilie8ORCID,Bedu Sébastien1ORCID,Tinevez Jean-Yves7ORCID,Baroud Charles56ORCID,Beaurepaire Emmanuel8ORCID,Bellaiche Yohanns3ORCID,Bally-Cuif Laure1ORCID,Dray Nicolas1ORCID

Affiliation:

1. Institut Pasteur, Université Paris Cité, CNRS UMR3738, Zebrafish Neurogenetics Unit, Team supported by the Ligue Nationale Contre le Cancer, Paris 75015, France.

2. Sorbonne Université, Collège Doctoral, Paris F-75005, France.

3. Institut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, Paris 75005, France.

4. LPSM, Sorbonne Université, UMR CNRS 8001, Paris 75005, France.

5. Institut Pasteur, Université Paris Cité, Physical Microfluidics and Bioengineering, Paris F-75015, France.

6. LadHyX, CNRS, Ecole Polytechnique, IP Paris, Palaiseau 91120, France.

7. Institut Pasteur, Université Paris Cité, Image Analysis Hub, Paris, France.

8. Laboratory for Optics and Biosciences, CNRS, INSERM, Ecole Polytechnique, IP Paris, Palaiseau, France.

Abstract

The maintenance of neural stem cells (NSCs) in the adult brain depends on their activation frequency and division mode. Using long-term intravital imaging of NSCs in the zebrafish adult telencephalon, we reveal that apical surface area and expression of the Notch ligand DeltaA predict these NSC decisions. deltaA -negative NSCs constitute a bona fide self-renewing NSC pool and systematically engage in asymmetric divisions generating a self-renewing deltaA neg daughter, which regains the size and behavior of its mother, and a neurogenic deltaA pos daughter, eventually engaged in neuronal production following further quiescence-division phases. Pharmacological and genetic manipulations of Notch, DeltaA, and apical size further show that the prediction of activation frequency by apical size and the asymmetric divisions of deltaA neg NSCs are functionally independent of Notch. These results provide dynamic qualitative and quantitative readouts of NSC lineage progression in vivo and support a hierarchical organization of NSCs in differently fated subpopulations.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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