Author:
Caldwell Megan,Ayo-Jibunoh Vanessa,Mendoza Josue Criollo,Brimblecombe Katherine R.,Reynolds Lauren M.,Zhu Jiang Xin Yan,Alarcon Colin,Fiore Elizabeth,N. Tomaio Jacquelyn,Phillips Greg R.,Mingote Susana,Flores Cecilia,Casaccia Patrizia,Liu Jia,Cragg Stephanie J.,McCloskey Dan P.,Yetnikoff Leora
Abstract
AbstractOligodendrocyte progenitor cells (OPCs) receive synaptic innervation from glutamatergic and GABAergic axons and can be dynamically regulated by neural activity, resulting in activity-dependent changes in patterns of axon myelination. However, it remains unclear to what extent other types of neurons may innervate OPCs. Here, we provide evidence implicating midbrain dopamine neurons in the innervation of oligodendrocyte lineage cells in the anterior corpus callosum and nearby white matter tracts of male and female adult mice. Dopaminergic axon terminals were identified in the corpus callosum of DAT-Cre mice after injection of an eYFP reporter virus into the midbrain. Furthermore, fast-scan cyclic voltammetry revealed monoaminergic transients in the anterior corpus callosum, consistent with the anatomical findings. Using RNAscope, we further demonstrate that ~ 40% of Olig2 + /Pdfgra + cells and ~ 20% of Olig2 + /Pdgfra- cells in the anterior corpus callosum express Drd1 and Drd2 transcripts. These results suggest that oligodendrocyte lineage cells may respond to dopamine released from midbrain dopamine axons, which could affect myelination. Together, this work broadens our understanding of neuron-glia interactions with important implications for myelin plasticity by identifying midbrain dopamine axons as a potential regulator of corpus callosal oligodendrocyte lineage cells.
Funder
Parkinson’s UK
National Institute on Drug Abuse at the National Institute of Health
Wellcome Trust
Aligning Science Across Parkinson’s
Medical Research Council
National Institute of Neurological Disorders and Stroke at the National Institute of Health
Publisher
Springer Science and Business Media LLC
Subject
Histology,General Neuroscience,Anatomy
Cited by
5 articles.
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