Fate mapping of neural stem cell niches reveals distinct origins of human cortical astrocytes

Author:

Allen Denise E.1234ORCID,Donohue Kevin C.25678ORCID,Cadwell Cathryn R.9ORCID,Shin David1234ORCID,Keefe Matthew G.1234ORCID,Sohal Vikaas S.278ORCID,Nowakowski Tomasz J.12347ORCID

Affiliation:

1. Department of Anatomy, University of California, San Francisco, CA, USA.

2. Department of Psychiatry and Behavioral Sciences, University of California, San Francisco, CA, USA.

3. Department of Neurological Surgery, University of California, San Francisco, CA, USA.

4. Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.

5. School of Medicine, University of California, San Francisco, CA, USA.

6. Center for Integrative Neuroscience, University of California, San Francisco, CA, USA.

7. Weill Institute for Neurosciences, University of California, San Francisco, CA, USA.

8. Kavli Institute for Fundamental Neuroscience, University of California, San Francisco, CA, USA.

9. Department of Pathology, University of California, San Francisco, CA, USA.

Abstract

Progenitors of the developing human neocortex reside in the ventricular and outer subventricular zones (VZ and OSVZ, respectively). However, whether cells derived from these niches have similar developmental fates is unknown. By performing fate mapping in primary human tissue, we demonstrate that astrocytes derived from these niches populate anatomically distinct layers. Cortical plate astrocytes emerge from VZ progenitors and proliferate locally, while putative white matter astrocytes are morphologically heterogeneous and emerge from both VZ and OSVZ progenitors. Furthermore, via single-cell sequencing of morphologically defined astrocyte subtypes using Patch-seq, we identify molecular distinctions between VZ-derived cortical plate astrocytes and OSVZ-derived white matter astrocytes that persist into adulthood. Together, our study highlights a complex role for cell lineage in the diversification of human neocortical astrocytes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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