🧫
Endothelium-specific TBK1 knockdown in atherosclerosis model
active
experiment
Created: 2026-04-11T00:51:12
By: etl-v1-backfill
Quality:
50%
✓ SciDEX
ID: exp-4e462be7-c43a-4f51-a7db-0b55d583c40a
🧫 Experiment Protocol
ValidationatherosclerosisTBK1endothelium-specific TBK1 knockdown miceproposed
Endothelium-specific TBK1 knockdown mice were generated and used to investigate the role of TBK1 in endothelial-to-mesenchymal transition and atherogenesis. The study examined the effects of reducing TBK1 expression specifically in endothelial cells on atherosclerotic plaque formation and endothelial dysfunction. This genetic approach allowed for tissue-specific investigation of TBK1's role while avoiding systemic effects that might confound results.
PRIMARY OUTCOME
effect of TBK1 knockdown on EndMT and plaque formation
EXPECTED OUTCOMES
## Expected Outcomes
### Primary Outcomes
1. **Enhanced atherosclerosis:** 30-50% increase in aortic lesion area in EC-TBK1-KD vs controls after 12 weeks Western diet
2. **Endothelial dysfunction:** Impaired ACh-induced vasorelaxation (e.g., 50% reduction in max relaxation)
3. **Increased permeability:** Evans blue extravasation elevated in aortas of KD mice
4. **Inflammation:** Upregulated VCAM-1, ICAM-1 expression in aortic endothelium
### Secondary Outcomes
- Larger lipid-rich necrotic cores in plaques of KD mice
- Reduced eNOS phosphorylation (indicative of reduced NO production)
- Elevated circulating inflammatory cytokines (TNF-α, IL-6)
### Null Result Interpretation
- If no phenotype, verify Cre recombination efficiency in endothelium
- Consider using inducible EC-specific TBK1 KO (VE-cadherin-CreERT2)
- May need longer HFD exposure (16-20 weeks) for robust phenotype
SUCCESS CRITERIA
## Success Criteria
### Primary
- [ ] TBK1 knockdown confirmed: ≥70% mRNA, ≥60% protein in MLECs
- [ ] ≥10/12 animals/group with complete histology and genotyping
- [ ] Aortic lesion area: ≥30% increase in KD vs control (p < 0.05)
- [ ] Endothelial relaxation: ≥30% reduction in ACh response
### Secondary
- [ ] Plasma lipid panel not significantly different between groups
- [ ] VCAM-1/ICAM-1 expression elevated in KD endothelium
- [ ] Blinded lesion quantification
### Technical Quality Gates
- [ ] Cre recombination confirmed by genotyping
- [ ] TBK1 expression unchanged in non-endothelial tissues
- [ ] Aortic ring viability confirmed (response to SNP intact)
PROTOCOL
## Protocol: Endothelium-Specific TBK1 Knockdown in Atherosclerosis Model
### Study Design
Validation study using endothelium-specific TBK1 knockdown mice on atherosclerosis-prone background to determine TBK1's role in endothelial dysfunction and atherogenesis.
### Animals and Breeding
1. Generate endothelium-specific TBK1 knockdown (EC-TBK1-KD) mice:
- Cross Tie2-Cre mice with TBK1-floxed mice (TBK1fl/fl)
- Genotype by PCR for Cre, TBK1fl allele
2. Cross onto Apoe-/- background for atherosclerosis susceptibility
3. Groups: EC-TBK1-KD/Apoe-/- (n=12) vs TBK1fl/fl/Apoe-/- controls (n=12)
4. Age and sex-matched (8 weeks old at study start)
5. Feed high-fat diet (Western diet, 0.2% cholesterol) for 12 weeks
### Endothelial Knockdown Validation
1. Isolate primary mouse lung endothelial cells (MLECs):
- Perfusion with collagenase, anti-CD31 magnetic bead purification
2. Confirm TBK1 knockdown:
- qPCR: TBK1 mRNA reduced ≥70% in EC-TBK1-KD vs controls
- Western blot: TBK1 protein reduced ≥60%
- Immunofluorescence: endothelial VE-cadherin+ cells show reduced TBK1
### Atherosclerosis Assessment
1. **Aortic en face analysis:**
- Perfuse mice with PBS, dissect aorta from arch to iliac bifurcation
- Stain with Sudan IV for lipid plaques
- Quantify lesion area (ImageJ) as % of total aortic area
2. **Aortic root sectioning:**
- OCT embedding, serial cryosections (10 µm)
- Oil Red O staining for neutral lipids
- Quantify lesion area in 5 sections per mouse at 100 µm intervals
3. **Plasma lipid analysis:**
- Collect plasma at sacrifice
- Measure total cholesterol, LDL, HDL, triglycerides (commercial kit)
### Endothelial Function Tests
1. **Aortic ring vasorelaxation assay:**
- Organ bath studies with acetylcholine (ACh) and sodium nitroprusside (SNP)
- Assess endothelium-dependent and independent relaxation
2. **Vascular permeability assay:**
- Evans blue dye injection, quantify leakage in aorta and organs
### Controls
- **Positive control:** Apoe-/- mice on Western diet (robust atherosclerosis)
- **Knockdown efficiency control:** TBK1 expression in non-endothelial tissues (liver, muscle)
- **Cre-negative control:** TBK1fl/fl without Cre (full TBK1 expression)
### Expected Outcomes
1. Increased atherosclerosis in EC-TBK1-KD mice (30-50% more aortic lesion area)
2. Impaired endothelium-dependent vasorelaxation (reduced ACh response)
3. Increased vascular permeability
4. Elevated systemic inflammation markers (VCAM-1, ICAM-1 upregulation)
### Success Criteria
- [ ] TBK1 knockdown ≥70% at mRNA level, ≥60% at protein level in endothelial cells
- [ ] ≥10/12 animals per group with confirmed knockdown and complete histology
- [ ] Significant increase in aortic lesion area (p < 0.05)
- [ ] Endothelial dysfunction confirmed (≥30% reduction in ACh-mediated relaxation)
- [ ] Plasma lipids comparable between groups (isolate TBK1 effect from lipid changes)
LINKED HYPOTHESES
Source: PMID 41685426 ↗
🧫 Experiment Extras
PATHWAY
endothelial-to-mesenchymal transition, atherogenesis
MARKET PRICE
$0.50
STATUS
proposed
▸Metadataorigin_type: v1_polymorphic_backfill
| origin_type | v1_polymorphic_backfill |
| source_table | experiments |
| _schema_version | 1 |
📊 Evidence Profile
Evidence Balance
+0%
Certainty
0%
Debates
0
Incoming
0
Outgoing
0
0 supporting
0 contradicting
0 neutral
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