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Maturation of the microglial population varies across mesolimbic nuclei.
Hope, Keenan T; Hawes, Isobel A; Moca, Eric N; Bonci, Antonello; De Biase, Lindsay M.
Affiliation
  • Hope KT; Department of Physiology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Hawes IA; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD, USA.
  • Moca EN; Department of Physiology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • De Biase LM; Department of Physiology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
Eur J Neurosci ; 52(7): 3689-3709, 2020 10.
Article de En | MEDLINE | ID: mdl-32281691
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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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Aire tegmentale ventrale / Microglie Limites: Animals Langue: En Journal: Eur J Neurosci Sujet du journal: NEUROLOGIA Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Aire tegmentale ventrale / Microglie Limites: Animals Langue: En Journal: Eur J Neurosci Sujet du journal: NEUROLOGIA Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique