Unique microglia recovery population revealed by single-cell RNAseq following neurodegeneration

Abstract Microglia are brain immune cells that constantly survey their environment to maintain homeostasis. Enhanced microglial reactivity and proliferation are typical hallmarks of neurodegenerative diseases. Whether specific disease-linked microglial subsets exist during the entire course of neuro...

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Main Authors: Tuan Leng Tay, Sagar, Jana Dautzenberg, Dominic Grün, Marco Prinz
Format: Article
Language:English
Published: BMC 2018-09-01
Series:Acta Neuropathologica Communications
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40478-018-0584-3
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spelling doaj-a44f9be75cb047d499ec955f4a9c2cc62020-11-25T02:35:11ZengBMCActa Neuropathologica Communications2051-59602018-09-016111110.1186/s40478-018-0584-3Unique microglia recovery population revealed by single-cell RNAseq following neurodegenerationTuan Leng Tay0Sagar1Jana Dautzenberg2Dominic Grün3Marco Prinz4Institute of Neuropathology, Faculty of Medicine, University of FreiburgMax-Planck-Institute of Immunobiology and EpigeneticsInstitute of Neuropathology, Faculty of Medicine, University of FreiburgMax-Planck-Institute of Immunobiology and EpigeneticsInstitute of Neuropathology, Faculty of Medicine, University of FreiburgAbstract Microglia are brain immune cells that constantly survey their environment to maintain homeostasis. Enhanced microglial reactivity and proliferation are typical hallmarks of neurodegenerative diseases. Whether specific disease-linked microglial subsets exist during the entire course of neurodegeneration, including the recovery phase, is currently unclear. Taking a single-cell RNA-sequencing approach in a susceptibility gene-free model of nerve injury, we identified a microglial subpopulation that upon acute neurodegeneration shares a conserved gene regulatory profile compared to previously reported chronic and destructive neurodegeneration transgenic mouse models. Our data also revealed rapid shifts in gene regulation that defined microglial subsets at peak and resolution of neurodegeneration. Finally, our discovery of a unique transient microglial subpopulation at the onset of recovery may provide novel targets for modulating microglia-mediated restoration of brain health.http://link.springer.com/article/10.1186/s40478-018-0584-3MicrogliaRecoveryNeurodegenerationSingle-cell RNA analysis
collection DOAJ
language English
format Article
sources DOAJ
author Tuan Leng Tay
Sagar
Jana Dautzenberg
Dominic Grün
Marco Prinz
spellingShingle Tuan Leng Tay
Sagar
Jana Dautzenberg
Dominic Grün
Marco Prinz
Unique microglia recovery population revealed by single-cell RNAseq following neurodegeneration
Acta Neuropathologica Communications
Microglia
Recovery
Neurodegeneration
Single-cell RNA analysis
author_facet Tuan Leng Tay
Sagar
Jana Dautzenberg
Dominic Grün
Marco Prinz
author_sort Tuan Leng Tay
title Unique microglia recovery population revealed by single-cell RNAseq following neurodegeneration
title_short Unique microglia recovery population revealed by single-cell RNAseq following neurodegeneration
title_full Unique microglia recovery population revealed by single-cell RNAseq following neurodegeneration
title_fullStr Unique microglia recovery population revealed by single-cell RNAseq following neurodegeneration
title_full_unstemmed Unique microglia recovery population revealed by single-cell RNAseq following neurodegeneration
title_sort unique microglia recovery population revealed by single-cell rnaseq following neurodegeneration
publisher BMC
series Acta Neuropathologica Communications
issn 2051-5960
publishDate 2018-09-01
description Abstract Microglia are brain immune cells that constantly survey their environment to maintain homeostasis. Enhanced microglial reactivity and proliferation are typical hallmarks of neurodegenerative diseases. Whether specific disease-linked microglial subsets exist during the entire course of neurodegeneration, including the recovery phase, is currently unclear. Taking a single-cell RNA-sequencing approach in a susceptibility gene-free model of nerve injury, we identified a microglial subpopulation that upon acute neurodegeneration shares a conserved gene regulatory profile compared to previously reported chronic and destructive neurodegeneration transgenic mouse models. Our data also revealed rapid shifts in gene regulation that defined microglial subsets at peak and resolution of neurodegeneration. Finally, our discovery of a unique transient microglial subpopulation at the onset of recovery may provide novel targets for modulating microglia-mediated restoration of brain health.
topic Microglia
Recovery
Neurodegeneration
Single-cell RNA analysis
url http://link.springer.com/article/10.1186/s40478-018-0584-3
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AT sagar uniquemicrogliarecoverypopulationrevealedbysinglecellrnaseqfollowingneurodegeneration
AT janadautzenberg uniquemicrogliarecoverypopulationrevealedbysinglecellrnaseqfollowingneurodegeneration
AT dominicgrun uniquemicrogliarecoverypopulationrevealedbysinglecellrnaseqfollowingneurodegeneration
AT marcoprinz uniquemicrogliarecoverypopulationrevealedbysinglecellrnaseqfollowingneurodegeneration
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