DOCK8 is expressed in microglia, and it regulates microglial activity during neurodegeneration in murine disease

Kazuhiko Namekata1, Xiaoli Guo1, Atsuko Kimura1

  • 1Visual Research Project, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan.

Insights

Dedicator of cytokinesis 8 (DOCK8) regulates microglial activity in the central nervous system. DOCK8 deficiency reduces neuroinflammation and cell death in models of multiple sclerosis and glaucoma.

Area of Science:

  • Neuroimmunology
  • Cell Biology

Background:

  • Dedicator of cytokinesis 8 (DOCK8) is crucial for immune function but its role in the central nervous system (CNS) is unknown.
  • Microglia, the resident immune cells of the CNS, are implicated in neurodegenerative diseases like multiple sclerosis (MS) and glaucoma.

Purpose of the Study:

  • To investigate the role of DOCK8 in microglial function within the CNS.
  • To determine DOCK8's involvement in neuroinflammation and neurodegenerative disease models.

Main Methods:

  • Expression analysis of DOCK8 in CNS cells.
  • Utilizing DOCK8-deficient mice in experimental autoimmune encephalomyelitis (EAE) and glaucoma models.
  • Assessing microglial migration, neuroinflammation severity, visual function, and retinal ganglion cell (RGC) survival.

Main Results:

  • DOCK8 is expressed in microglia and upregulated during neuroinflammation.
  • DOCK8-deficient mice showed reduced microglial migration in optic neuritis models.
  • DOCK8 deficiency decreased neuroinflammation severity, improved visual function, and reduced RGC death in MS/optic neuritis models.
  • Impaired microglial phagocytosis of RGCs was observed in DOCK8-deficient mice during glaucoma modeling.

Conclusions:

  • DOCK8 is a key regulator of microglial activity in the CNS during disease states.
  • DOCK8 plays a significant role in microglial migration and phagocytosis.
  • Targeting DOCK8 may offer therapeutic potential for neuroinflammatory and neurodegenerative diseases like MS and glaucoma.

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