| Literature DB >> 28689984 |
Lindsay M De Biase1, Kornel E Schuebel2, Zachary H Fusfeld3, Kamwing Jair2, Isobel A Hawes3, Raffaello Cimbro4, Hai-Ying Zhang3, Qing-Rong Liu3, Hui Shen3, Zheng-Xiong Xi3, David Goldman2, Antonello Bonci5.
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. Published by Elsevier Inc.Entities:
Keywords: RNA sequencing; density; development; electrophysiology; heterogeneity; microglia; morphology; nucleus accumbens; substantia nigra; ventral tegmental area
Mesh:
Year: 2017 PMID: 28689984 PMCID: PMC5754189 DOI: 10.1016/j.neuron.2017.06.020
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173