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      Neuron-Glia Signaling in Synapse Elimination

      1 , 1 , 1 , 2 , 3
      Annual Review of Neuroscience
      Annual Reviews

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          Abstract

          Maturation of neuronal circuits requires selective elimination of synaptic connections. Although neuron-intrinsic mechanisms are important in this process, it is increasingly recognized that glial cells also play a critical role. Without proper functioning of these cells, the number, morphology, and function of synaptic contacts are profoundly altered, resulting in abnormal connectivity and behavioral abnormalities. In addition to their role in synaptic refinement, glial cells have also been implicated in pathological synapse loss and dysfunction following injury or nervous system degeneration in adults. Although mechanisms regulating glia-mediated synaptic elimination are still being uncovered, it is clear this complex process involves many cues that promote and inhibit the removal of specific synaptic connections. Gaining a greater understanding of these signals and the contribution of different cell types will not only provide insight into this critical biological event but also be instrumental in advancing knowledge of brain development and neural disease.

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          Author and article information

          Journal
          Annual Review of Neuroscience
          Annu. Rev. Neurosci.
          Annual Reviews
          0147-006X
          1545-4126
          July 08 2019
          July 08 2019
          : 42
          : 1
          : 107-127
          Affiliations
          [1 ]Department of Neurology and F.M. Kirby Neurobiology Center, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA;
          [2 ]Stanley Center, Broad Institute, Cambridge, Massachusetts 02142, USA
          [3 ]Howard Hughes Medical Institute, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA
          Article
          10.1146/annurev-neuro-070918-050306
          31283900
          3887b625-9cdc-49bf-9a0f-b4c1130cc943
          © 2019
          History

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