About this item:

111 Views | 82 Downloads

Author Notes:

Correspondence: Francisco J. Alvarez, francisco.j.alvarez@emory.edu

Author contributions: Study Design: T.M.R. and F.J.A., Histology, imaging and analyses: T.M.R. and F.J.A. Manuscript writing: F.J.A. and T.M.R. Figure design and production: T.M.R. and F.J.A.

We thank Ms. Alicia Lane for editing this manuscript and also for contributing some of the sections with immunolabeled synaptic markers for analyses included in Figure 7.

Disclosures: The authors declare no competing interests.

Subjects:

Research Funding:

This work was supported by NIH-NINDS R56NS099092 grant (FJA) and Ruth L. Kirschstein NRSA F31NS095528 & F32NS112556 fellowships (TMR).

Two-photon microscope and analysis packages used in this study were made available by the Integrated Cellular Imaging Microscopy Core at Emory University.

This core is in part supported by NINDS Core facilities grant P30NS055077.

Keywords:

  • Science & Technology
  • Multidisciplinary Sciences
  • Science & Technology - Other Topics
  • Facial motor nucleus
  • Spinal cord injury
  • Synaptic plasticity
  • Cell death
  • Activated microglia
  • Axonal dieback
  • Neuron death
  • In-situ
  • Brain
  • Phagocytosis

Microglia Dynamics and Interactions with Motoneurons Axotomized After Nerve Injuries Revealed By Two-Photon Imaging

Tools:

Journal Title:

Scientific Reports

Volume:

Volume 10, Number 1

Publisher:

, Pages 8648-8648

Type of Work:

Article | Final Publisher PDF

Abstract:

The significance of activated microglia around motoneurons axotomized after nerve injuries has been intensely debated. In particular, whether microglia become phagocytic is controversial. To resolve these issues we directly observed microglia behaviors with two-photon microscopy in ex vivo spinal cord slices from CX3CR1-GFP mice complemented with confocal analyses of CD68 protein. Axotomized motoneurons were retrogradely-labeled from muscle before nerve injuries. Microglia behaviors close to axotomized motoneurons greatly differ from those within uninjured motor pools. They develop a phagocytic phenotype as early as 3 days after injury, characterized by frequent phagocytic cups, high phagosome content and CD68 upregulation. Interactions between microglia and motoneurons changed with time after axotomy. Microglia first extend processes that end in phagocytic cups at the motoneuron surface, then they closely attach to the motoneuron while extending filopodia over the cell body. Confocal 3D analyses revealed increased microglia coverage of the motoneuron cell body surface with time after injury and the presence of CD68 granules in microglia surfaces opposed to motoneurons. Some microglia formed macroclusters associated with dying motoneurons. Microglia in these clusters display the highest CD68 expression and associate with cytotoxic T-cells. These observations are discussed in relation to current theories on microglia function around axotomized motoneurons.

Copyright information:

© The Author(s) 2020.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
Export to EndNote