Mapping and kinetics of microglia/neuron cell-to-cell contacts in the 6-OHDA murine model of Parkinson's disease

Glia. 2013 Oct;61(10):1645-58. doi: 10.1002/glia.22546. Epub 2013 Jul 25.

Abstract

As neuroinflammatory processes are involved in the pathogenesis of Parkinson's disease (PD), we provide several key data describing the time-course of microglial accumulation in relation with behavioral alterations and neurodegeneration in a murine model of PD induced by intrastriatal injection of 6-hydroxydopamine (6-OHDA). Our study argues for a major role of microglia which accumulation is somehow early and transient in spite of the neuronal loss progression. Moreover, we observed less 6-OHDA-induced neurodegeneration associated with less inflammatory reaction in DAP-12 Knock-In mice. The direct cell-to-cell contacts that may support physical interactions between microglia and altered dopaminergic neurons are ill-defined, while it is currently hypothesized that microglia support an immune-mediated amplification of neurodegeneration by establishing a molecular cross talk with neurons. Indeed, we sought to map microglia/neuron appositions in substantia nigra (SN) of 6-OHDA injected C57Bl/6 mice and CX3CR1/(GFP/+) mice. Confocal immunofluorescence analyses followed by 3D reconstitutions reveal close appositions between the soma of TH+ neurons and microglial cell bodies and ramifications. Interestingly, some microglial ramifications penetrated TH(+) somas and about 40% of GFP(+) microglial cells in the injured SN harbored TH(+) intracytoplasmic inclusions. These results suggest a direct cross talk between neurons and microglia that may exert a microphagocytic activity toward TH+ neurons. Altogether, these results obtained in a murine PD model may participate in the understanding of microglial cells' function in neurodegenerative diseases.

Keywords: dopamine; neurodegeneration; neuroinflammation; substantia nigra.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adrenergic Agents / toxicity*
  • Animals
  • Antigens, Differentiation / metabolism
  • Apomorphine
  • Cell Communication / drug effects
  • Cell Communication / genetics
  • Cell Communication / physiology*
  • Cell Count
  • Disease Models, Animal
  • Dopamine Agonists
  • Female
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Imaging, Three-Dimensional
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microglia / cytology
  • Microglia / drug effects
  • Microglia / physiology*
  • Microscopy, Confocal
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / physiology*
  • Oxidopamine / toxicity*
  • Parkinson Disease* / etiology
  • Parkinson Disease* / genetics
  • Parkinson Disease* / pathology
  • Receptors, Interleukin-8A / deficiency
  • Rotation
  • Substantia Nigra / pathology
  • Time Factors
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Adrenergic Agents
  • Antigens, Differentiation
  • Dopamine Agonists
  • Receptors, Interleukin-8A
  • Tyrobp protein, mouse
  • monocyte-macrophage differentiation antigen
  • Green Fluorescent Proteins
  • Oxidopamine
  • Tyrosine 3-Monooxygenase
  • Apomorphine