The laminar position, morphology, and gene expression profiles of cortical astrocytes are influenced by time of birth from ventricular/subventricular progenitors

Author:

Lozano Casasbuenas Daniela12ORCID,Kortebi Ines13,Gora Charles4,Scott Erica Y.156,Gomes Celeste1,Oliveira Markley Silva7,Sharma Tanvi1,Daniele Emerson13,Olfat Arman1,Gibbs Rachel13,Yuzwa Scott A.2,Gilbert Emily A.1,Küry Patrick78ORCID,Wheeler Aaron R.569ORCID,Lévesque Martin4ORCID,Faiz Maryam123ORCID

Affiliation:

1. Division of Anatomy, Department of Surgery University of Toronto Toronto Ontario Canada

2. Department of Laboratory Medicine and Pathobiology University of Toronto Toronto Ontario Canada

3. Institute of Medical Science University of Toronto Toronto Ontario Canada

4. Department of Psychiatry and Neurosciences Université Laval, Québec, Canada; CERVO Brain Research Center Québec Canada

5. Department of Chemistry University of Toronto Toronto Ontario Canada

6. Donnelly Centre for Cellular and Biomolecular Research University of Toronto Toronto Ontario Canada

7. Neuroregeneration Laboratory, Department of Neurology, Medical Faculty Heinrich‐Heine University Düsseldorf Germany

8. Department of Neurology, Inselspital Bern University Hospital and University of Bern Bern Switzerland

9. Institute of Biomedical Engineering University of Toronto Toronto Ontario Canada

Abstract

AbstractAstrocytes that reside in superficial (SL) and deep cortical layers have distinct molecular profiles and morphologies, which may underlie specific functions. Here, we demonstrate that the production of SL and deep layer (DL) astrocyte populations from neural progenitor cells in the mouse is temporally regulated. Lineage tracking following in utero and postnatal electroporation with PiggyBac (PB) EGFP and birth dating with EdU and FlashTag, showed that apical progenitors produce astrocytes during late embryogenesis (E16.5) that are biased to the SL, while postnatally labeled (P0) astrocytes are biased to the DL. In contrast, astrocytes born during the predominantly neurogenic window (E14.5) showed a random distribution in the SL and DL. Of interest, E13.5 astrocytes birth dated at E13.5 with EdU showed a lower layer bias, while FT labeling of apical progenitors showed no bias. Finally, examination of the morphologies of “biased” E16.5‐ and P0‐labeled astrocytes demonstrated that E16.5‐labeled astrocytes exhibit different morphologies in different layers, while P0‐labeled astrocytes do not. Differences based on time of birth are also observed in the molecular profiles of E16.5 versus P0‐labeled astrocytes. Altogether, these results suggest that the morphological, molecular, and positional diversity of cortical astrocytes is related to their time of birth from ventricular/subventricular zone progenitors.

Funder

Natural Sciences and Engineering Research Council of Canada

Jürgen Manchot Stiftung

Canadian Institutes of Health Research

Fonds de recherche du Québec

Genome Canada

Publisher

Wiley

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