Maturation of the microglial population varies across mesolimbic nuclei.

Eur J Neurosci

Department of Physiology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.

Published: October 2020

AI Article Synopsis

  • Microglia undergo significant changes in their characteristics as they develop from embryos to adults, particularly in how they distribute in brain regions and their activation states.
  • A study explored the maturation of microglia in specific areas of the basal ganglia in mice, revealing that microglial density peaks during the third week after birth due to rapid cell growth.
  • In the nucleus accumbens (NAc), this increase is more pronounced than in the ventral tegmental area (VTA) and is linked to a higher number of lysosomes, highlighting a crucial period for microglial development that may influence brain circuitry and vulnerability to inflammation.

Article Abstract

Microglia play critical roles during CNS development and undergo dramatic changes in tissue distribution, morphology, and gene expression as they transition from embryonic to neonatal to adult microglial phenotypes. Despite the magnitude of these phenotypic shifts, little is known about the time course and dynamics of these transitions and whether they vary across brain regions. Here, we define the time course of microglial maturation in key regions of the basal ganglia in mice, where significant regional differences in microglial phenotype are present in adults. We found that microglial density peaks in the ventral tegmental area (VTA) and nucleus accumbens (NAc) during the third postnatal week, driven by a burst of microglial proliferation. Microglial abundance is then refined to adult levels through a combination of tissue expansion and microglial programmed cell death. This overproduction and refinement of microglia was significantly more pronounced in the NAc than in the VTA and was accompanied by a sharp peak in NAc microglial lysosome abundance in the third postnatal week. Collectively, these data identify a key developmental window when elevated microglial density in discrete basal ganglia nuclei may support circuit refinement and could increase susceptibility to inflammatory insults.

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http://dx.doi.org/10.1111/ejn.14740DOI Listing

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