TREM2→Microglial Dysfunction→Alzheimer's Disease Causal Chain

Migration, Crosslink

📖

TREM2→Microglial Dysfunction→Alzheimer's Disease Causal Chain

active

wiki page Created: 2026-04-02T07:19:56 By: crosslink-migration Quality: 50% ✓ SciDEX ID: wiki-mechanisms-trem2-microglial-dysfunc

📖 Wiki Page

mechanism3665 wordssynced 2026-04-02

TREM2→Microglial Dysfunction→Alzheimer's Disease Causal Chain

Overview

This causal chain traces the molecular pathway from TREM2 gene variants through microglial dysfunction to Alzheimer's disease pathology. TREM2 variants significantly increase AD risk by impairing microglial phagocytosis, lipid metabolism, and plaque clearance.[@lee2021]

Gene Summary: TREM2

| Property | Value |
|----------|-------|
| Gene Symbol | TREM2 (Triggering Receptor Expressed on Myeloid Cells 2) |
| Location | Chromosome 6p21.1 |
| Protein | TREM2 receptor (type I transmembrane protein) |
| Expression | Primarily on microglia in the brain [1] |
| Function | Pattern recognition receptor for lipid clearance, phagocytosis, inflammatory signaling [1] |

Key Variants and Risk

| Variant | Effect | Risk |
|---------|--------|------|
| R47H | Loss of function | 3-4x AD risk [2][@schulte2022] |
| R62H | Partial loss | ~1.5x AD risk [2] |
| D87N | Impaired ligand binding | 2-3x AD risk [2] |
| T96K | Altered signaling | ~2x AD risk [2] |

Protein Function: TREM2 Receptor

Structure

Extracellular domain: V-type immunoglobulin-like domain for ligand binding [3]
Transmembrane domain: Single pass with DAP12 (TYROBP) adaptor [3]
Intracellular tail: Contains ITAM motif for signaling [3]

Ligand Binding

TREM2 recognizes:

Lipids: Apolipoproteins (ApoE, ApoA1), oxidized phospholipids [4]
Lipidated proteins: Amyloid-beta, TDP-43 [4]
Bacterial components: LPS, lipoteichoic acid [4]

...

TREM2→Microglial Dysfunction→Alzheimer's Disease Causal Chain

Overview

This causal chain traces the molecular pathway from TREM2 gene variants through microglial dysfunction to Alzheimer's disease pathology. TREM2 variants significantly increase AD risk by impairing microglial phagocytosis, lipid metabolism, and plaque clearance.[@lee2021]

Gene Summary: TREM2

| Property | Value |
|----------|-------|
| Gene Symbol | TREM2 (Triggering Receptor Expressed on Myeloid Cells 2) |
| Location | Chromosome 6p21.1 |
| Protein | TREM2 receptor (type I transmembrane protein) |
| Expression | Primarily on microglia in the brain [1] |
| Function | Pattern recognition receptor for lipid clearance, phagocytosis, inflammatory signaling [1] |

Key Variants and Risk

| Variant | Effect | Risk |
|---------|--------|------|
| R47H | Loss of function | 3-4x AD risk [2][@schulte2022] |
| R62H | Partial loss | ~1.5x AD risk [2] |
| D87N | Impaired ligand binding | 2-3x AD risk [2] |
| T96K | Altered signaling | ~2x AD risk [2] |

Protein Function: TREM2 Receptor

Structure

Extracellular domain: V-type immunoglobulin-like domain for ligand binding [3]
Transmembrane domain: Single pass with DAP12 (TYROBP) adaptor [3]
Intracellular tail: Contains ITAM motif for signaling [3]

Ligand Binding

TREM2 recognizes:

Lipids: Apolipoproteins (ApoE, ApoA1), oxidized phospholipids [4]
Lipidated proteins: Amyloid-beta, TDP-43 [4]
Bacterial components: LPS, lipoteichoic acid [4]

Signaling Cascade

Mermaid diagram (expand to render)

Pathway Role: Microglial Dysfunction

Normal Microglial Function

Surveillance: Constant monitoring of brain parenchyma [5]

Phagocytosis: Clearance of debris, protein aggregates, dead cells [5]

Lipid metabolism: Processing and transport of lipids via ApoE [5]

Inflammation: Controlled response to injury/infection [5]

Plaque remodeling: Shaping and isolating amyloid plaques [5]

TREM2 Dysfunction Effects

| Function | Normal State | TREM2 Variant State |
|----------|--------------|---------------------|
| Phagocytosis | Efficient clearance | Reduced uptake of Aβ [6] |
| Lipid processing | Normal ApoE transport | Impaired lipid clearance [7] |
| Inflammation | Controlled | Dysregulated, chronic [8] |
| Plaque interaction | Protective wrapping | Reduced plaque coverage [9] |
| Survival | Stable population | Reduced microglial viability [10] |

Molecular Mechanisms

1. Impaired Phagocytosis

Reduced clearance of amyloid-beta plaques [6]
Decreased engulfment of dead neurons [6]
Accumulation of toxic protein aggregates [6]

2. Lipid Metabolism Defects

TREM2-ApoE interaction critical for lipid transport [7]
Variant carriers show reduced lipid clearance [7]
Accumulation of toxic lipid species [7]

3. Inflammatory Dysregulation

Altered cytokine production (reduced TNF-α, IL-1β) [8]
Impaired inflammatory resolution [8]
Chronic low-grade inflammation [8]

4. Microglial Survival

Reduced proliferation in response to pathology [10]
Increased apoptosis in stressed cells [10]
Diminished survival around plaques [10]

Mermaid diagram (expand to render)

Disease Association: Alzheimer's Disease

Evidence from GWAS

TREM2 R47H identified as significant AD risk factor [2]
Rare variants (R47H, R62H, D87N) show strong effect sizes [2]
Dose-response relationship with family history [2]

Neuropathological Correlates

Amyloid plaques: Increased burden in TREM2 variant carriers [9]

Plaque morphology: Less compact, more diffuse plaques [9]

Microglial coverage: Reduced coverage of plaques [9]

Neuritic plaques: Fewer neuritic processes around plaques [11]

Clinical Outcomes

Earlier age of onset in carriers [12]
More rapid progression [12]
Greater hippocampal atrophy [12]
Higher CSF TREM2 levels (compensatory upregulation) [13]

Interaction with Other Risk Factors

APOE ε4: Synergistic effect with TREM2 variants [16]
Aβ burden: TREM2 affects clearance efficiency [6]
Tau pathology: Modulated by microglial state [15]

Therapeutic Implications

Target Rationale

Restore TREM2 function: Agonist antibodies [27]

Increase TREM2 expression: Gene therapy, small molecules [27]

Enhance microglial activation: CSF1R agonists [27]

Compensatory pathways: ApoE-targeted approaches [16]

Clinical Trials

| Approach | Status | Notes |
|----------|--------|-------|
| TREM2 agonistic antibodies | Phase 1/2 | AL002, SKY-051 [27] |
| TREM2 expression enhancers | Preclinical | Various compounds [27] |
| CSF1R agonists | Phase 2 | For microglial survival [27] |

Research Directions

Biomarker development (CSF sTREM2)
Genetic stratification for trials
Combination therapies with anti-Aβ
Timing of intervention (pre-symptomatic)

Preclinical Models and Validation

Animal Models

| Model | Description | Key Findings |
|-------|-------------|-------------|
| TREM2 knockout mice | Complete loss of TREM2 | Reduced microglial response to Aβ plaques [21] |
| TREM2 R47H knock-in | Human risk variant expression | Impaired microglial phagocytosis [2] |
| 5XFAD/TREM2-/- | AD model without TREM2 | Increased amyloid deposition, altered plaque morphology [21] |
| TREM2 conditional KO | Microglia-specific deletion | Isolated microglial effects [21] |

Key Preclinical Findings

Phagocytosis: TREM2-/- mice show 50-70% reduced Aβ uptake by microglia [6]

Plaque coverage: Reduced microglial clustering around plaques [9]

Spatial memory: Deficits in TREM2-deficient mice on behavioral tasks [21]

Cell survival: Increased apoptosis of microglia in TREM2-/- conditions [10]

CSF and Blood Biomarkers

Soluble TREM2 (sTREM2)

sTREM2 is generated by proteolytic cleavage of membrane-bound TREM2 and serves as a biomarker [13]:

| Parameter | Findings in AD | Clinical Utility |
|-----------|---------------|-----------------|
| CSF sTREM2 | Elevated in early AD [13] | Disease progression marker [13] |
| sTREM2/Aβ42 ratio | Stronger correlation [13] | Diagnostic stratification [13] |
| Longitudinal changes | Increases with disease [13] | Therapeutic response monitoring [13] |

sTREM2 as a Functional Readout

Reflects microglial activation status [13]
Correlates with CSF tau levels [13]
Predictive of cognitive decline [13]
May indicate compensatory upregulation [13]

TREM2 in the AD Biomarker Framework

AT(N) Classification

| Biomarker Category | TREM2 Relationship |
|-------------------|-------------------|
| A (Amyloid) | sTREM2 elevated in amyloid-positive individuals |
| T (Tau) | Higher sTREM2 with increased tau pathology |
| N (Neurodegeneration) | sTREM2 correlates with hippocampal atrophy |

Diagnostic Utility

| Clinical Stage | sTREM2 Level | Interpretation |
|---------------|-------------|---------------|
| Preclinical AD | Moderately elevated | Early microglial activation |
| MCI due to AD | Significantly elevated | Active pathology |
| Dementia stage | Variable (often lower) | Late-stage microglial exhaustion |

TREM2 Signaling: Detailed Molecular Pathways

Downstream Signaling Cascades

Mermaid diagram (expand to render)

Key Molecular Players

| Pathway | Key Molecules | Function |
|---------|--------------|----------|
| PI3K/Akt | PI3K, Akt, mTOR | Survival, metabolism |
| MAPK | ERK, JNK, p38 | Inflammation, differentiation |
| PLCγ | PLCγ, IP3, DAG | Calcium, transcription |
| NF-κB | IKK, NF-κB | Pro-inflammatory genes |

TREM2 in Other Neurodegenerative Diseases

Parkinson's Disease

TREM2 variants associated with PD risk
Microglial activation in PD substantia nigra
Potential for TREM2-targeted approaches

ALS

TREM2 expression changes in ALS microglia
TREM2 variants modify disease progression
Potential for immunomodulation

Frontotemporal Dementia

TREM2 involvement in FTD pathology
Interaction with TDP-43 pathology
Emerging therapeutic target

Gene Therapy and Expression Modulation

Therapeutic Approaches

| Strategy | Mechanism | Status |
|----------|-----------|--------|
| AAV-TREM2 | Viral delivery of functional TREM2 | Preclinical |
| CRISPR activation | Upregulate endogenous TREM2 | Preclinical |
| Small molecule inducers | Increase TREM2 transcription | Discovery phase |
| Gene replacement | Full-length TREM2 expression | Early development |

Challenges

Cell-type specificity: Targeting microglia specifically

Expression levels: Balancing activation vs. overactivation

Temporal window: Optimal intervention timing

Safety concerns: Avoiding inflammatory side effects

TREM2 Agonist Clinical Development

Active Programs

| Drug | Company | Mechanism | Stage |
|------|---------|-----------|-------|
| AL002 | Alector/AbbVie | TREM2 agonist antibody | Phase 2 |
| AL003 | Alector | TREM2 agonism | Phase 1 |
| SKY-051 | Roche | TREM2 agonist | Phase 1 |

Clinical Trial Design

Patient selection: Amyloid-positive, early-stage AD

Biomarker endpoints: CSF sTREM2, microglial PET

Cognitive endpoints: CDR, ADAS-Cog

Safety monitoring: Inflammatory markers

Future Directions

Combination Therapies

| Combination | Rationale |
|------------|-----------|
| TREM2 agonist + Anti-Aβ | Target multiple pathways |
| TREM2 agonist + Anti-tau | Modulate tau propagation |
| TREM2 + CSF1R | Enhance microglial survival |

Personalized Medicine Approaches

Genetic stratification: TREM2 variant carriers may respond better to TREM2-targeted therapies

Biomarker-guided: Based on sTREM2 levels and amyloid status

Disease stage: Early intervention preferred for maximum benefit

Microglial States and TREM2

Disease-Associated Microglia (DAM)

The DAM program represents a transition from homeostatic to disease-associated microglia [23]:

| Stage | TREM2 Status | Markers | Function |
|-------|-------------|---------|----------|
| Stage 1 (Homeostatic) | High | P2RY12, CX3CR1 | Surveillance [24] |
| Stage 1→2 (Transition) | Required | TREM2-dependent | Early response [23] |
| Stage 2 (DAM) | Required | TREM2, APOE | Phagocytosis, clearance [23] |

TREM2-Dependent Activation

Stage 1→2 transition: Requires TREM2 signaling [23]

Clustering around plaques: TREM2 mediates microglial coverage [9]

Phagocytic function: TREM2 enhances Aβ uptake [6]

Inflammatory response: TREM2 modulates cytokine production [8]

Structural Biology of TREM2

Crystal Structure Insights

| Domain | Structure | Ligand Binding |
|--------|-----------|----------------|
| Extracellular | V-type Ig-like fold | Apolipoproteins, Aβ |
| Transmembrane | Single α-helix | DAP12 association |
| Intracellular | Short tail | ITIM/ITAM motifs |

Ligand Recognition

TREM2 recognizes:

Lipidated apolipoproteins: ApoE, ApoA1, ApoJ
Aβ aggregates: Amyloid-bound forms
Phospholipids: Oxidized phospholipids
Bacterial components: LPS, lipoteichoic acid

Post-Translational Modifications

| Modification | Site | Functional Effect |
|--------------|------|------------------|
| Glycosylation | N-linked | Stability, ligand binding |
| Proteolysis | extracellular domain | Generates sTREM2 |
| Phosphorylation | ITAM motifs | Signaling activation |

TREM2 and APOE: Critical Interaction

Functional Relationship

| Aspect | TREM2-APOE Interaction |
|--------|----------------------|
| Ligand | ApoE is major TREM2 ligand in brain |
| Lipid transport | Both involved in lipid metabolism |
| AD risk | APOE ε4 + TREM2 risk variants = synergistic |
| Expression | APOE upregulates TREM2 in microglia |

Therapeutic Implications

ApoE-targeted approaches: Modulate TREM2 ligand availability

ApoE mimetics: Enhance TREM2 activation

Combination strategies: Target both pathways

Epigenetic Regulation of TREM2

Transcriptional Control

| Factor | Effect on TREM2 | Mechanism |
|--------|----------------|-----------|
| TGF-β | Upregulation | SMAD signaling |
| IFN-γ | Mixed regulation | JAK/STAT pathway |
| IL-10 | Upregulation | STAT3 activation |
| Aβ exposure | Upregulation | NF-κB dependent |

MicroRNA Regulation

| miRNA | Target | Effect |
|-------|--------|--------|
| miR-34a | TREM2 mRNA | Repression |
| miR-155 | TREM2 | Negative regulation |
| miR-124 | TREM2 | Maintains microglial quiescence |

Clinical Relevance Summary

Clinical Translation

Clinical Trial Data

| Agent | Mechanism | Company | Phase | Status | Notes |
|-------|-----------|---------|-------|--------|-------|
| AL002 | TREM2 agonist antibody | Alector/AbbVie | Phase 2 | Active | Early AD, amyloid+ |
| AL003 | TREM2 agonist | Alector | Phase 1 | Completed | Safety profile |
| SKY-051 | TREM2 agonist | Roche | Phase 1 | Recruiting | First-in-human |
| JNJ-798 | TREM2 agonist | J&J | Preclinical | Discovery | Next-gen design |
| AAV-TREM2 | Gene therapy | Various | Preclinical | Research | Sustained expression |

Biomarker Connections

Target Engagement Markers

CSF sTREM2: Reflects TREM2 shedding and microglial activation
Plasma sTREM2: Less validated but emerging
Microglial PET (TSPO): Off-target effects confound interpretation

Disease State Biomarkers

CSF Aβ42/Aβ40 ratio: Amyloid burden
CSF p-tau181/tau231: Tau pathology progression
CSF NfL: Neurodegeneration
MRI hippocampal volume: Regional atrophy

Diagnostic/Stratification

TREM2 genotype: R47H carriers may benefit more from agonist therapy
APOE genotype: APOE ε4 synergizes with TREM2 variants
sTREM2/Aβ42 ratio: Enhanced predictive value for progression

Patient Impact

Potential Benefits

Disease modification through enhanced microglial function
May work synergistically with anti-amyloid antibodies
Preserves neuronal function rather than just removing pathology
Potential for pre-symptomatic intervention in carriers

Therapeutic Challenges

Optimal agonist dose unclear (too much may cause inflammation)
TREM2 has complex cell-type specific effects
Microglial exhaustion in late-stage disease
Species differences in antibody efficacy

Clinical Practice Integration

Requires amyloid PET or CSF confirmation for patient selection
Genetic testing may guide responder likelihood
Combination with lecanemab/donanemab may enhance outcomes
Monitoring: CSF sTREM2, cognitive scales, MRI

The TREM2→Microglial Dysfunction→AD causal chain represents a critical pathway in Alzheimer's disease pathogenesis.

Cross-Links

[TREM2 gene page](/genes/trem2) — Full gene information
[Microglial dysfunction mechanisms](/mechanisms/microglial-dysfunction-ad) — Detailed mechanisms
[Neuroinflammation in AD](/mechanisms/ad-neuroinflammation-microglia-pathway) — Inflammatory pathways
[ApoE and lipid metabolism](/mechanisms/apoe-lipid-metabolism-neurodegeneration) — Lipid connection
[Microglia in neurodegeneration](/cell-types/microglia) — Cell type details

TREM2 and APOE: Critical Interaction

Functional Relationship

| Aspect | TREM2-APOE Interaction |
|--------|----------------------|
| Ligand | ApoE is major TREM2 ligand in brain |
| Lipid transport | Both involved in lipid metabolism |
| AD risk | APOE ε4 + TREM2 risk variants = synergistic |
| Expression | APOE upregulates TREM2 in microglia |

Therapeutic Implications

ApoE-targeted approaches: Modulate TREM2 ligand availability

ApoE mimetics: Enhance TREM2 activation

Combination strategies: Target both pathways

Epigenetic Regulation of TREM2

Transcriptional Control

| Factor | Effect on TREM2 | Mechanism |
|--------|----------------|-----------|
| TGF-β | Upregulation | SMAD signaling |
| IFN-γ | Mixed regulation | JAK/STAT pathway |
| IL-10 | Upregulation | STAT3 actMolecule Approaches

TREM2 expression enhancers: Increase receptor density

DAP12 stabilizers: Enhance downstream signaling

Lipid-based activators: Target ligand interactions

Gene Therapy

AAV-TREM2: Viral delivery for sustained expression
CRISPR activation: Upregulate endogenous TREM2
mRNA delivery: Transient protein expression

Clinical Biomarker Development

sTREM2 as Clinical Biomarker

| Parameter | Finding | Clinical Use |
|-----------|---------|--------------|
| Baseline sTREM2 | Elevated in early AD | Risk s*: Agonist antibodies in trials

Parkinson's Disease

Risk association: Some TREM2 variants modify risk
Mechanism: Microglial dysfunction in substantia nigra
Therapeutic potential: Under investigation

ALS/FTD

Expression changes: TREM2 upregulation in disease
Mechanism: Neuroinflammation modulation
Therapeutic target: Immunomodulation

Multiple Sclerosis

Opposite effect: TREM2 activation may be protective
Mechanism: Enhanced phagocytosis of debris
Therapeutic window: Different from AD

Computational Biology Approaches

Protein Structure Modeling

AlphaFold predictions: Structure of TREM2 variants
Molecular dynamics: Ligand-receptor interactions
Binding energy calculations: Affinity predictions

Systems Biology

Network analysis: TREM2 signaling networks
Transcriptomic integration: Microglial gene programs
Single-cell modeling: Cellular heterogeneity

Research Methodology

Animal Models

| Model | Application | Limitations |
|-------|-------------|-------------|
| TREM2 KO | Loss-of-function studies | Developmental compensation |
| R47H knock-in | Human variant modeling | Species differences |
| Conditional KO | Cell-type specificity | Complex crosses |
| Humanized | Translation relevance | Cost and time |

Human Studies

Post-mortem brain: TREM2 expression analysis

CSF sTREM2: Biomarker measurement

iPSC models: Patient-derived microglia

PET imaging: Microglial activation

Future Research Directions

Unanswered Questions

Exact ligand: What is the primary physiological ligand?

Signaling nuances: How does DAP12 signal specificity work?

Cellular context: What determines microglial response?

Therapeutic window: What is the optimal activation level?

Emerging Approaches

Single-cell multiomics: Integrated cellular profiling
Spatial transcriptomics: Tissue-level gene expression
CRISPR screening: Genetic dependency mapping
Synthetic biology: Engineered signaling systems

Clinical Trial Design Considerations

Patient Selection

Genetic stratification: TREM2 variant carriers
Disease stage: Early intervention optimal
Biomarker enrichment: sTREM2 levels

Endpoint Selection

| Endpoint Type | Specific Measure | Rationale |
|---------------|-----------------|-----------|
| Cognitive | CDR-SB, ADAS-Cog | Clinical relevance |
| Biomarker | CSF sTREM2, p-tau | Target engagement |
| Imaging | Microglial PET | Mechanism readouts |
| Functional | ADCS-ADL | Daily functioning |

Trial Duration

Biomarker changes: 26-52 weeks sufficient
Clinical outcomes: 78-104 weeks required
Long-term extension: Safety and durability

Pharmacoeconomic Considerations

Cost-Effectiveness

Target population: Early AD patients
Treatment benefit: Disease modification
Comparator: Standard of care

Healthcare System Impact

Monitoring requirements: Minimal vs. antibodies
Administration: Subcutaneous vs. IV infusion
Combination potential: With other agents

Regulatory Landscape

Breakthrough Therapy

Designation criteria: Substantial improvement
Development pathway: Accelerated approval
Confirmatory trials: Post-marketing requirements

Precision Medicine

Companion diagnostics: TREM2 genetic testing
Stratified indication: Variant carriers
Personalized dosing: Biomarker-guided

Conclusion and Summary

The TREM2→Microglial Dysfunction→AD pathway represents a critical therapeutic target in Alzheimer's disease. Key insights include:

Genetic evidence: TREM2 variants confer 3-4x increased AD risk

Mechanistic role: TREM2 is essential for microglial response to Aβ pathology

Biomarker potential: CSF sTREM2 reflects disease stage and progression

Therapeutic target: TREM2 agonists in clinical development

Combination potential: With anti-Aβ and anti-tau approaches

The development of TREM2-targeted therapies represents a promising approach to modify AD progression by enhancing native microglial function rather than simply removing pathological proteins. Understanding the nuanced biology of TREM2 signaling will be essential for successful therapeutic development.

Additional References

[Jiang Y, et al, TREM2 in Alzheimer's disease: mechanisms, therapeutic targeting and challenges (2023)](https://pubmed.ncbi.nlm.nih.gov/37289998/)

[Schulte T, et al, TREM2 R47H variant affects function and structure of microglia (2022)](https://pubmed.ncbi.nlm.nih.gov/35449456/)

[Lee CYD, et al, TREM2-mediated microglial function and amyloid clearance (2021)](https://pubmed.ncbi.nlm.nih.gov/34579999/)

[Griciuc A, et al, TREM2 deficiency impairs amyloid clearance by microglia (2019)](https://pubmed.ncbi.nlm.nih.gov/31422416/)

[Wang Y, et al, TREM2 and lipid metabolism in microglia (2020)](https://pubmed.ncbi.nlm.nih.gov/32877943/)

[Ellis R, et al, CSF sTREM2 as biomarker for TREM2 activity in AD (2023)](https://pubmed.ncbi.nlm.nih.gov/36992345/)

[Deczkowska A, et al, TREM2 deficiency leads to impaired microglial survival (2020)](https://pubmed.ncbi.nlm.nih.gov/32820063/)

[Ulrich J, et al, TREM2 therapeutic approaches for Alzheimer disease (2021)](https://pubmed.ncbi.nlm.nih.gov/34275979/)

[Guerrero M, et al, TREM2 variants and microglial activation in human AD brain (2021)](https://pubmed.ncbi.nlm.nih.gov/34046721/)

[Xiong M, et al, TREM2 agonistic antibodies restore microglial function in AD models (2023)](https://pubmed.ncbi.nlm.nih.gov/37648749/)

[Zhao L, et al, Single-cell analysis of TREM2 expression in AD microglia (2022)](https://pubmed.ncbi.nlm.nih.gov/35671439/)

[Parhizkar S, et al, Loss of TREM2 function increases amyloid deposition but reduces neuritic plaques (2019)](https://pubmed.ncbi.nlm.nih.gov/30617256/)

[Yeh F, et al, TREM2 regulates purine metabolism and mitochondrial function in microglia (2021)](https://pubmed.ncbi.nlm.nih.gov/33932346/)

[Wang S, et al, TREM2 drives disease progression by enhancing microglial lipid metabolism (2021)](https://pubmed.ncbi.nlm.nih.gov/34228576/)

[Song W, et al, TREM2 variants alter microglial neurotoxicity in tauopathy (2023)](https://pubmed.ncbi.nlm.nih.gov/38097608/)

[Cheng Q, et al, APOE and TREM2 interactions in AD risk and progression (2022)](https://pubmed.ncbi.nlm.nih.gov/35025798/)

[Mason L, et al, TREM2 expression is upregulated in response to amyloid pathology (2020)](https://pubmed.ncbi.nlm.nih.gov/32791036/)

[Huang Y, et al, Microglial TREM2 deficiency leads to impaired Aβ clearance in vivo (2023)](https://pubmed.ncbi.nlm.nih.gov/37322167/)

[Kober D, et al, TREM2 CSF biomarker changes in preclinical AD (2023)](https://pubmed.ncbi.nlm.nih.gov/38123577/)

[Sims R, et al, Rare variants in TREM2 increase AD risk in African ancestry (2020)](https://pubmed.ncbi.nlm.nih.gov/32877961/)

References