Peripherally derived macrophages can engraft the brain independent of irradiation and maintain an identity distinct from microglia

Author:

Cronk James C.1234,Filiano Anthony J.12,Louveau Antoine12,Marin Ioana123,Marsh Rachel12,Ji Emily12,Goldman Dylan H.123,Smirnov Igor12ORCID,Geraci Nicholas1ORCID,Acton Scott5,Overall Christopher C.12,Kipnis Jonathan1234ORCID

Affiliation:

1. Center for Brain Immunology and Glia (BIG), University of Virginia, Charlottesville, VA

2. Department of Neuroscience, University of Virginia, Charlottesville, VA

3. Graduate Program in Neuroscience, University of Virginia, Charlottesville, VA

4. Medical Scientist Training Program, University of Virginia, Charlottesville, VA

5. Virginia Image and Video Analysis Laboratory, Department of Electrical and Computer Engineering and Department of Biomedical Engineering, University of Virginia, Charlottesville, VA

Abstract

Peripherally derived macrophages infiltrate the brain after bone marrow transplantation and during central nervous system (CNS) inflammation. It was initially suggested that these engrafting cells were newly derived microglia and that irradiation was essential for engraftment to occur. However, it remains unclear whether brain-engrafting macrophages (beMφs) acquire a unique phenotype in the brain, whether long-term engraftment may occur without irradiation, and whether brain function is affected by the engrafted cells. In this study, we demonstrate that chronic, partial microglia depletion is sufficient for beMφs to populate the niche and that the presence of beMφs does not alter behavior. Furthermore, beMφs maintain a unique functional and transcriptional identity as compared with microglia. Overall, this study establishes beMφs as a unique CNS cell type and demonstrates that therapeutic engraftment of beMφs may be possible with irradiation-free conditioning regimens.

Funder

National Institutes of Health

Hartwell Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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