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.
Abstract:
Dedicator of cytokinesis 8 (DOCK8) is a guanine nucleotide exchange factor whose loss of function results in immunodeficiency, but its role in the central nervous system (CNS) has been unclear. Microglia are the resident immune cells of the CNS and are implicated in the pathogenesis of various neurodegenerative diseases, including multiple sclerosis (MS) and glaucoma, which affects the visual system. However, the exact roles of microglia in these diseases remain unknown. Herein, we report that DOCK8 is expressed in microglia but not in neurons or astrocytes and that its expression is increased during neuroinflammation. To define the role of DOCK8 in microglial activity, we focused on the retina, a tissue devoid of infiltrating T cells. The retina is divided into distinct layers, and in a disease model of MS/optic neuritis, DOCK8-deficient mice exhibited a clear reduction in microglial migration through these layers. Moreover, neuroinflammation severity, indicated by clinical scores, visual function, and retinal ganglion cell (RGC) death, was reduced in the DOCK8-deficient mice. Furthermore, using a glaucoma disease model, we observed impaired microglial phagocytosis of RGCs in DOCK8-deficient mice. Our data demonstrate that DOCK8 is expressed in microglia and regulates microglial activity in disease states. These findings contribute to a better understanding of the molecular pathways involved in microglial activation and implicate a role of DOCK8 in several neurological diseases.
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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