학술논문

The P522R protective variant of PLCG2 promotes the expression of antigen presentation genes by human microglia in an Alzheimer's disease mouse model
Document Type
article
Source
Alzheimer's & Dementia. 18(10)
Subject
Biomedical and Clinical Sciences
Immunology
Prevention
Stem Cell Research - Induced Pluripotent Stem Cell - Human
Aging
Genetics
Acquired Cognitive Impairment
Dementia
Neurodegenerative
Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD)
Stem Cell Research
Stem Cell Research - Induced Pluripotent Stem Cell
Neurosciences
Alzheimer's Disease
Brain Disorders
2.1 Biological and endogenous factors
Aetiology
Neurological
Animals
Humans
Mice
Alzheimer Disease
Amyloid beta-Peptides
Antigen Presentation
CD8-Positive T-Lymphocytes
Chemokines
Disease Models
Animal
Induced Pluripotent Stem Cells
Mice
Transgenic
Microglia
CCL8
chimeric Alzheimer's mouse model
human leukocyte antigen
human stem cell-derived microglia
MHCII
PLCG2
T cells
Clinical Sciences
Geriatrics
Clinical sciences
Biological psychology
Language
Abstract
The P522R variant of PLCG2, expressed by microglia, is associated with reduced risk of Alzheimer's disease (AD). Yet, the impact of this protective mutation on microglial responses to AD pathology remains unknown. Chimeric AD and wild-type mice were generated by transplanting PLCG2-P522R or isogenic wild-type human induced pluripotent stem cell microglia. At 7 months of age, single-cell and bulk RNA sequencing, and histological analyses were performed. The PLCG2-P522R variant induced a significant increase in microglial human leukocyte antigen (HLA) expression and the induction of antigen presentation, chemokine signaling, and T cell proliferation pathways. Examination of immune-intact AD mice further demonstrated that the PLCG2-P522R variant promotes the recruitment of CD8+ T cells to the brain. These data provide the first evidence that the PLCG2-P522R variant increases the capacity of microglia to recruit T cells and present antigens, promoting a microglial transcriptional state that has recently been shown to be reduced in AD patient brains.