Department of Neurobiology and Behavior, Irvine, United States; Institute for Memory Impairments and Neurological Disorders, Irvine, United States
Allison R Najafi
Department of Neurobiology and Behavior, Irvine, United States; Institute for Memory Impairments and Neurological Disorders, Irvine, United States
Yasamine Ghorbanian
Sue and Bill Gross Stem Cell Research Center, Irvine, United States; Department of Molecular Biology and Biochemistry, Irvine, United States
Neelakshi Soni
Department of Neurobiology and Behavior, Irvine, United States; Institute for Memory Impairments and Neurological Disorders, Irvine, United States
Joshua Crapser
Department of Neurobiology and Behavior, Irvine, United States; Institute for Memory Impairments and Neurological Disorders, Irvine, United States
Dario X Figueroa Velez
Department of Neurobiology and Behavior, Irvine, United States
Shan Jiang
Department of Developmental and Cell Biology, Irvine, United States
Sarah E Royer
Department of Neurobiology and Behavior, Irvine, United States; Sue and Bill Gross Stem Cell Research Center, Irvine, United States; Department of Anatomy and Neurobiology, Irvine, United States
Sung Jin Kim
Department of Neurobiology and Behavior, Irvine, United States; Institute for Memory Impairments and Neurological Disorders, Irvine, United States
Caden M Henningfield
Department of Neurobiology and Behavior, Irvine, United States; Institute for Memory Impairments and Neurological Disorders, Irvine, United States
Department of Neurobiology and Behavior, Irvine, United States; Institute for Memory Impairments and Neurological Disorders, Irvine, United States; Sue and Bill Gross Stem Cell Research Center, Irvine, United States; Department of Anatomy and Neurobiology, Irvine, United States; Department of Physical Medicine & Rehabilitation, University of California, Irvine, Irvine, United States
Sunil P Gandhi
Department of Neurobiology and Behavior, Irvine, United States
Ali Mortazavi
Department of Developmental and Cell Biology, Irvine, United States
Matthew A Inlay
Department of Neurobiology and Behavior, Irvine, United States; Sue and Bill Gross Stem Cell Research Center, Irvine, United States; Department of Molecular Biology and Biochemistry, Irvine, United States
Microglia, the brain’s resident myeloid cells, play central roles in brain defense, homeostasis, and disease. Using a prolonged colony-stimulating factor 1 receptor inhibitor (CSF1Ri) approach, we report an unprecedented level of microglial depletion and establish a model system that achieves an empty microglial niche in the adult brain. We identify a myeloid cell that migrates from the subventricular zone and associated white matter areas. Following CSF1Ri, these amoeboid cells migrate radially and tangentially in a dynamic wave filling the brain in a distinct pattern, to replace the microglial-depleted brain. These repopulating cells are enriched in disease-associated microglia genes and exhibit similar phenotypic and transcriptional profiles to white-matter-associated microglia. Our findings shed light on the overlapping and distinct functional complexity and diversity of myeloid cells of the CNS and provide new insight into repopulating microglia function and dynamics in the mouse brain.