CSF1R inhibitor PLX3397 depletes microglia in Mongolian gerbil Meriones unguiculatus, but not in syrian hamster Mesocricetus auratus

J Pharmacol Sci. 2024 Jun;155(2):29-34. doi: 10.1016/j.jphs.2024.03.003. Epub 2024 Mar 23.

Abstract

Microglia are the residential immune cells in the central nervous system. Their roles as innate immune cells and regulators of synaptic remodeling are critical to the development and the maintenance of the brain. Numerous studies have depleted microglia to elucidate their involvement in healthy and pathological conditions. PLX3397, a blocker of colony stimulating factor 1 receptor (CSF1R), is widely used to deplete mouse microglia due to its non-invasiveness and convenience. Recently, other small rodents, including Syrian hamsters (Mesocricetus auratus) and Mongolian gerbils (Meriones unguiculatus), have been recognized as valuable animal models for studying brain functions and diseases. However, whether microglia depletion via PLX3397 is feasible in these species remains unclear. Here, we administered PLX3397 orally via food pellets to hamsters and gerbils. PLX3397 successfully depleted gerbil microglia but had no effect on microglial density in hamsters. Comparative analysis of the CSF1R amino acid sequence in different species hints that amino acid substitutions in the juxtamembrane domain may potentially contribute to the inefficacy of PLX3397 in hamsters.

Keywords: Colony stimulating factor 1 receptor; Microglia; Mongolian gerbil; PLX3397; Syrian hamster.

MeSH terms

  • Administration, Oral
  • Aminopyridines*
  • Animals
  • Brain / cytology
  • Brain / drug effects
  • Brain / metabolism
  • Cricetinae
  • Gerbillinae*
  • Male
  • Mesocricetus*
  • Microglia* / drug effects
  • Microglia* / metabolism
  • Models, Animal
  • Pyrroles* / pharmacology
  • Pyrrolidines / pharmacology
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor* / antagonists & inhibitors
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor* / genetics
  • Species Specificity

Substances

  • pexidartinib
  • Receptors, Granulocyte-Macrophage Colony-Stimulating Factor
  • Pyrroles
  • Pyrrolidines
  • Aminopyridines