Microglia and Central Nervous System–Associated Macrophages—From Origin to Disease Modulation

Author:

Prinz Marco123,Masuda Takahiro4,Wheeler Michael A.56,Quintana Francisco J.56

Affiliation:

1. Institute of Neuropathology, Faculty of Medicine, University of Freiburg, D-79106 Freiburg, Germany;

2. Center for Basics in NeuroModulation (NeuroModulBasics), Faculty of Medicine, University of Freiburg, D-79106 Freiburg, Germany

3. BIOSS Centre for Biological Signalling Studies and Centre for Integrative Biological Signalling Studies (CIBSS), University of Freiburg, D-79104 Freiburg, Germany

4. Department of Molecular and System Pharmacology, Graduate School of Pharmaceutical Sciences, Kyushu University, 812-8582 Fukuoka, Japan;

5. Ann Romney Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA;,

6. Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA

Abstract

The immune system of the central nervous system (CNS) consists primarily of innate immune cells. These are highly specialized macrophages found either in the parenchyma, called microglia, or at the CNS interfaces, such as leptomeningeal, perivascular, and choroid plexus macrophages. While they were primarily thought of as phagocytes, their function extends well beyond simple removal of cell debris during development and diseases. Brain-resident innate immune cells were found to be plastic, long-lived, and host to an outstanding number of risk genes for multiple pathologies. As a result, they are now considered the most suitable targets for modulating CNS diseases. Additionally, recent single-cell technologies enhanced our molecular understanding of their origins, fates, interactomes, and functional cell statesduring health and perturbation. Here, we review the current state of our understanding and challenges of the myeloid cell biology in the CNS and treatment options for related diseases.

Publisher

Annual Reviews

Subject

Immunology,Immunology and Allergy

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