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Local Cues Establish and Maintain Region-Specific Phenotypes of Basal Ganglia Microglia.
De Biase, Lindsay M; Schuebel, Kornel E; Fusfeld, Zachary H; Jair, Kamwing; Hawes, Isobel A; Cimbro, Raffaello; Zhang, Hai-Ying; Liu, Qing-Rong; Shen, Hui; Xi, Zheng-Xiong; Goldman, David; Bonci, Antonello.
Affiliation
  • De Biase LM; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA. Electronic address: lindsay.debiase@nih.gov.
  • Schuebel KE; Intramural Research Program, Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, MD 20852, USA.
  • Fusfeld ZH; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
  • Jair K; Intramural Research Program, Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, MD 20852, USA.
  • Hawes IA; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
  • Cimbro R; Division of Rheumatology, Bayview Flow Cytometry Core, Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA.
  • Zhang HY; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
  • Liu QR; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
  • Shen H; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
  • Xi ZX; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA.
  • Goldman D; Intramural Research Program, Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, MD 20852, USA.
  • Bonci A; Intramural Research Program, National Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, USA; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins
Neuron ; 95(2): 341-356.e6, 2017 Jul 19.
Article de En | MEDLINE | ID: mdl-28689984
ABSTRACT
Microglia play critical roles in tissue homeostasis and can also modulate neuronal function and synaptic connectivity. In contrast to astrocytes and oligodendrocytes, which arise from multiple progenitor pools, microglia arise from yolk sac progenitors and are widely considered to be equivalent throughout the CNS. However, little is known about basic properties of deep brain microglia, such as those within the basal ganglia (BG). Here, we show that microglial anatomical features, lysosome content, membrane properties, and transcriptomes differ significantly across BG nuclei. Region-specific phenotypes of BG microglia emerged during the second postnatal week and were re-established following genetic or pharmacological microglial ablation and repopulation in the adult, indicating that local cues play an ongoing role in shaping microglial diversity. These findings demonstrate that microglia in the healthy brain exhibit a spectrum of distinct functional states and provide a critical foundation for defining microglial contributions to BG circuit function.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Noyaux gris centraux / Microglie Limites: Animals Langue: En Journal: Neuron Sujet du journal: NEUROLOGIA Année: 2017 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Noyaux gris centraux / Microglie Limites: Animals Langue: En Journal: Neuron Sujet du journal: NEUROLOGIA Année: 2017 Type de document: Article
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