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Molecular architecture of the mouse nervous system

View ORCID ProfileAmit Zeisel, View ORCID ProfileHannah Hochgerner, Peter Lönnerberg, Anna Johnsson, View ORCID ProfileFatima Memic, Job van der Zwan, View ORCID ProfileMartin Häring, Emelie Braun, View ORCID ProfileLars Borm, View ORCID ProfileGioele La Manno, View ORCID ProfileSimone Codeluppi, View ORCID ProfileAlessandro Furlan, View ORCID ProfileNathan Skene, Kenneth D. Harris, View ORCID ProfileJens Hjerling Leffler, View ORCID ProfileErnest Arenas, View ORCID ProfilePatrik Ernfors, View ORCID ProfileUlrika Marklund, View ORCID ProfileSten Linnarsson
doi: https://doi.org/10.1101/294918
Amit Zeisel
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Hannah Hochgerner
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Peter Lönnerberg
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Anna Johnsson
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Fatima Memic
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Job van der Zwan
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Martin Häring
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Emelie Braun
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Lars Borm
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Gioele La Manno
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Simone Codeluppi
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Alessandro Furlan
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Nathan Skene
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Kenneth D. Harris
2Department of Neuroscience, Physiology, and Pharmacology, University College London, London WC1E 6BT, UK.
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Jens Hjerling Leffler
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Ernest Arenas
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Patrik Ernfors
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Ulrika Marklund
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Sten Linnarsson
1Division of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, S-17177 Stockholm, Sweden
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Abstract

The mammalian nervous system executes complex behaviors controlled by specialised, precisely positioned and interacting cell types. Here, we used RNA sequencing of half a million single cells to create a detailed census of cell types in the mouse nervous system. We mapped cell types spatially and derived a hierarchical, data-driven taxonomy. Neurons were the most diverse, and were grouped by developmental anatomical units, and by the expression of neurotransmitters and neuropeptides. Neuronal diversity was driven by genes encoding cell identity, synaptic connectivity, neurotransmission and membrane conductance. We discovered several distinct, regionally restricted, astrocytes types, which obeyed developmental boundaries and correlated with the spatial distribution of key glutamate and glycine neurotransmitters. In contrast, oligodendrocytes showed a loss of regional identity, followed by a secondary diversification. The resource presented here lays a solid foundation for understanding the molecular architecture of the mammalian nervous system, and enables genetic manipulation of specific cell types.

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Posted April 06, 2018.
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Molecular architecture of the mouse nervous system
Amit Zeisel, Hannah Hochgerner, Peter Lönnerberg, Anna Johnsson, Fatima Memic, Job van der Zwan, Martin Häring, Emelie Braun, Lars Borm, Gioele La Manno, Simone Codeluppi, Alessandro Furlan, Nathan Skene, Kenneth D. Harris, Jens Hjerling Leffler, Ernest Arenas, Patrik Ernfors, Ulrika Marklund, Sten Linnarsson
bioRxiv 294918; doi: https://doi.org/10.1101/294918
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Molecular architecture of the mouse nervous system
Amit Zeisel, Hannah Hochgerner, Peter Lönnerberg, Anna Johnsson, Fatima Memic, Job van der Zwan, Martin Häring, Emelie Braun, Lars Borm, Gioele La Manno, Simone Codeluppi, Alessandro Furlan, Nathan Skene, Kenneth D. Harris, Jens Hjerling Leffler, Ernest Arenas, Patrik Ernfors, Ulrika Marklund, Sten Linnarsson
bioRxiv 294918; doi: https://doi.org/10.1101/294918

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