Single-cell profiling identifies myeloid cell subsets with distinct fates during neuroinflammation

Author:

Jordão Marta Joana Costa12ORCID,Sankowski Roman13ORCID,Brendecke Stefanie M.1ORCID,Sagar 4,Locatelli Giuseppe56,Tai Yi-Heng56,Tay Tuan Leng127ORCID,Schramm Eva1,Armbruster Stephan1,Hagemeyer Nora1,Groß Olaf18910,Mai Dominic1112,Çiçek Özgün11,Falk Thorsten811ORCID,Kerschensteiner Martin5613ORCID,Grün Dominic4,Prinz Marco181014

Affiliation:

1. Institute of Neuropathology, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

2. Faculty of Biology, University of Freiburg, Freiburg, Germany.

3. Berta-Ottenstein-Programme, Faculty of Medicine, University of Freiburg, Germany.

4. Max-Planck-Institute of Immunobiology and Epigenetics, Freiburg, Germany.

5. Institute of Clinical Neuroimmunology, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany.

6. Biomedical Center (BMC), Faculty of Medicine, Ludwig-Maximilians University Munich, Munich, Germany.

7. Cluster of Excellence BrainLinks-BrainTools, University of Freiburg, Freiburg, Germany.

8. BIOSS Centre for Biological Signalling Studies, University of Freiburg, Germany.

9. Institute of Clinical Chemistry and Pathobiochemistry, University Hospital Rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.

10. CIBSS Centre for Integrative Biological Signalling Studies, University of Freiburg, Germany.

11. Institute of Computer Science, University of Freiburg, Freiburg, Germany.

12. Life Imaging Center, Center for Biological Systems Analysis, Albert-Ludwigs University, Freiburg, Germany.

13. Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.

14. Centre for NeuroModulation, University of Freiburg, Germany.

Abstract

A myeloid cell atlas of neuroinflammation Myeloid cells, such as dendritic cells and macrophages, in the central nervous system (CNS) play critical roles in the initiation and exacerbation of multiple sclerosis (MS). Jordão et al. combined high-throughput single-cell RNA sequencing and intravital microscopy to compile a transcriptional atlas of myeloid subsets in experimental autoimmune encephalomyelitis (EAE), a mouse model of MS. Microglia and other CNS-associated macrophages expanded and transformed into various context-dependent subtypes during EAE. Furthermore, dendritic cells and monocyte-derived cells, but not resident macrophages, played a critical role by presenting antigen to pathogenic T cells. This exhaustive characterization may inform future therapeutic targeting strategies in MS. Science , this issue p. eaat7554

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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