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A set of vocabulary-style flashcards covering key microglia concepts from the lecture notes.
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Microglia
Brain-resident immune cells that monitor the CNS environment; originate from yolk sac progenitors and self-renew in the brain.
Surveillant microglia
Resting, ramified microglia that continuously patrol the brain parenchyma for signs of trouble.
Synaptic pruning
Microglia-mediated removal of excess or weak synapses during development, often involving complement signaling.
Phagocytosis
Engulfment and digestion of dead cells, debris, or synaptic material by microglia.
Apoptotic cell clearance
Microglia remove dying cells during development and in the adult brain through phagocytosis.
Dendritic cell (brain)
Antigen-presenting cell listed among brain macrophage subpopulations.
Meningeal macrophage
Macrophage population located in the meninges surrounding the CNS.
Perivascular macrophage
Macrophages in the perivascular space around brain blood vessels.
Choroid plexus macrophage
Macrophages in the choroid plexus involved in CSF surveillance.
Monocyte-derived macrophage
Macrophages that originate from circulating monocytes and can infiltrate the CNS during inflammation.
Yolk sac hematopoiesis
Embryonic source of microglial precursors in the yolk sac before CNS colonization.
Fetal liver monocytes
Hematopoietic source contributing to monocyte/macrophage lineage during development.
Self-renewal
Microglia maintain their population in the brain by dividing themselves, with limited input from bone marrow.
Steady-state brain
Normal, non-diseased brain with microglia in a surveillant, homeostatic state.
Inflamed brain
Brain in which microglia adopt activated transcriptional programs and inflammatory functions.
Core transcriptional module
Conserved set of microglial genes defining baseline identity across species.
Environment-dependent transcriptional module
Microglial gene programs that vary with brain environment and include GWAS hits for AD/PD/MS.
DAM (Disease-Associated Microglia)
Microglial transcriptional state enriched in neurodegenerative disease, often TREM2-dependent.
MGnD
Microglia phenotype linked to neurodegeneration; related to DAM in several studies.
TREM2
Microglial receptor promoting transition toward disease-associated/microglial activation states.
P2ry12
Purine receptor marking homeostatic microglia; often downregulated in disease-associated states.
MerTK
Receptor tyrosine kinase important for phagocytosis, including apoptotic cell clearance by microglia.
APOE
Apolipoprotein E; genetic risk factor for Alzheimer's disease; expressed by microglia in disease states.
Spp1 (osteopontin)
Gene upregulated in certain activated microglial states; involved in inflammatory responses.
Lgals3 (galectin-3)
Glycoprotein involved in microglial activation and phagocytosis.
Gpnmb
Gene expressed in microglial activation states, part of the MGnD signature.
Pu.1 (Spi1)
Transcription factor essential for myeloid/microglial lineage commitment.
SALL1
Transcription factor marking homeostatic microglia.
Tmem119
Microglia-specific surface marker used to identify microglia in studies.
CX3CR1
Fractalkine receptor on microglia; mediates neuron-microglia communication and surveillance.
CX3CL1
Fractalkine; neuronal ligand for CX3CR1.
CD200/CD200R
Signaling axis that maintains microglial quiescence and limits activation.
SIRPα/CD47
“Don’t eat me” signals that restrain microglial phagocytosis.
PAMPs
Pathogen-associated molecular patterns that activate microglia via innate receptors.
DAMPs
Damage-associated molecular patterns released by stressed/dying cells to activate microglia.
LPS
Bacterial endotoxin used experimentally to trigger microglial inflammatory responses.
Pro-inflammatory cytokines
Cytokines such as IL-1β, IL-6, and TNF-α produced by activated microglia.
Anti-inflammatory mediators
Cytokines like IL-10 that promote anti-inflammatory responses and tissue protection.
Resting microglia
Microglia in a surveillant, homeostatic state with ramified morphology.
Activated microglia
Microglia that shift to pro- or anti-inflammatory states in response to challenges.
Chronic neurodegenerative diseases
Long-term brain diseases (e.g., Alzheimer’s, Parkinson’s) in which microglia contribute to pathology.
Complement pathway in pruning
System that tags synapses for removal by microglia via receptors like CR3.
CR3
Complement receptor 3 on microglia involved in synaptic pruning; KO reduces engulfment.