Faculty, Staff and Student Publications
Publication Date
4-23-2024
Journal
Cell Reports
Abstract
Border-associated macrophages (BAMs) are tissue-resident macrophages that reside at the border of the central nervous system (CNS). Since BAMs originate from yolk sac progenitors that do not persist after birth, the means by which this population of cells is maintained is not well understood. Using two-photon microscopy and multiple lineage-tracing strategies, we determine that CCR2+ monocytes are significant contributors to BAM populations following disruptions of CNS homeostasis in adult mice. After BAM depletion, while the residual BAMs possess partial self-repopulation capability, the CCR2+ monocytes are a critical source of the repopulated BAMs. In addition, we demonstrate the existence of CCR2+ monocyte-derived long-lived BAMs in a brain compression model and in a sepsis model after the initial disruption of homeostasis. Our study reveals that the short-lived CCR2+ monocytes transform into long-lived BAM-like cells at the CNS border and subsequently contribute to BAM populations.
Keywords
Animals, Receptors, CCR2, Monocytes, Macrophages, Mice, Brain, Mice, Inbred C57BL, Homeostasis
DOI
10.1016/j.celrep.2024.114120
PMID
38625796
PMCID
PMC11105166
PubMedCentral® Posted Date
5-20-2024
PubMedCentral® Full Text Version
Author MSS
Published Open-Access
yes