CSF-1 controls cerebellar microglia and is required for motor function and social interaction

Author:

Kana Veronika123,Desland Fiona A.123,Casanova-Acebes Maria123ORCID,Ayata Pinar45ORCID,Badimon Ana45ORCID,Nabel Elisa4678,Yamamuro Kazuhiko4678,Sneeboer Marjolein910,Tan I-Li11,Flanigan Meghan E.4,Rose Samuel A.12,Chang Christie123,Leader Andrew123ORCID,Le Bourhis Hortense123,Sweet Eric S.4ORCID,Tung Navpreet123,Wroblewska Aleksandra12ORCID,Lavin Yonit123,See Peter13ORCID,Baccarini Alessia12,Ginhoux Florent13,Chitu Violeta14ORCID,Stanley E. Richard14ORCID,Russo Scott J.4,Yue Zhenyu4,Brown Brian D.12,Joyner Alexandra L.11,De Witte Lotje D.6910,Morishita Hirofumi4678,Schaefer Anne45,Merad Miriam123ORCID

Affiliation:

1. Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY

2. Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY

3. Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY

4. Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY

5. Ronald M. Loeb Center for Alzheimer’s Disease, Icahn School of Medicine at Mount Sinai, New York, NY

6. Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY

7. Department of Ophthalmology, Icahn School of Medicine at Mount Sinai, New York, NY

8. Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY

9. Department of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands

10. Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands

11. Developmental Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY

12. Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY

13. Singapore Immunology Network, Agency for Science, Technology, and Research, Singapore

14. Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY

Abstract

Microglia, the brain resident macrophages, critically shape forebrain neuronal circuits. However, their precise function in the cerebellum is unknown. Here we show that human and mouse cerebellar microglia express a unique molecular program distinct from forebrain microglia. Cerebellar microglial identity was driven by the CSF-1R ligand CSF-1, independently of the alternate CSF-1R ligand, IL-34. Accordingly, CSF-1 depletion from Nestin+ cells led to severe depletion and transcriptional alterations of cerebellar microglia, while microglia in the forebrain remained intact. Strikingly, CSF-1 deficiency and alteration of cerebellar microglia were associated with reduced Purkinje cells, altered neuronal function, and defects in motor learning and social novelty interactions. These findings reveal a novel CSF-1–CSF-1R signaling-mediated mechanism that contributes to motor function and social behavior.

Funder

National Institutes of Health

Swiss National Foundation

Human Frontier Science Program Organization

National Institute of Mental Health

National Eye Institute

National Institute of Neurological Disorders and Stroke

Naito Foundation

Uehara Memorial Foundation

Seaver Foundation

National Research Foundation Senior Investigatorship

Singapore Immunology Network Core Funding

EMBO

Brain and Behavior Research Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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