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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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 |
work_keys_str_mv |
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