CNS macrophages differentially rely on an intronic Csf1r enhancer for their development

Development. 2020 Dec 15;147(23):dev194449. doi: 10.1242/dev.194449.

Abstract

The central nervous system hosts parenchymal macrophages, known as microglia, and non-parenchymal macrophages, collectively termed border-associated macrophages (BAMs). Microglia, but not BAMs, were reported to be absent in mice lacking a conserved Csf1r enhancer: the fms-intronic regulatory element (FIRE). However, it is unknown whether FIRE deficiency also impacts BAM arrival and/or maintenance. Here, we show that macrophages in the ventricular system of the brain, including Kolmer's epiplexus macrophages, are absent in Csf1rΔFIRE/ΔFIRE mice. Stromal choroid plexus BAMs are also considerably reduced. During normal development, we demonstrate that intracerebroventricular macrophages arrive from embryonic day 10.5, and can traverse ventricular walls in embryonic slice cultures. In Csf1rΔFIRE/ΔFIRE embryos, the arrival of both primitive microglia and intracerebroventricular macrophages was eliminated, whereas the arrival of cephalic mesenchyme and stromal choroid plexus BAMs was only partially restricted. Our results provide new insights into the development and regulation of different CNS macrophage populations.

Keywords: CNS-associated macrophages; Cerebral ventricles; Cerebrospinal fluid; Kolmer cells; Myeloid cells; Phagocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain / growth & development
  • Brain / metabolism
  • Central Nervous System / growth & development
  • Embryo, Mammalian
  • Embryonic Development / genetics*
  • Enhancer Elements, Genetic / genetics*
  • Introns / genetics
  • Macrophages / metabolism*
  • Mice
  • Microglia / metabolism
  • Parenchymal Tissue / growth & development
  • Parenchymal Tissue / metabolism
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor / genetics*
  • Regulatory Sequences, Nucleic Acid

Substances

  • Csf1r protein, mouse
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor