APP-London model
Take advantage of InnoSer’s expanded neurology CRO services spanning new Alzheimer’s in vivo research models and expertise
Key characteristics
- Progressive β-amyloid plaque development at a later age (from 10 months) in cortex, hippocampus and subiculum
- Pyroglutamate-modified Aβ42 (Aβ3(pE)-42) is detected in the insoluble brain fraction from 12 months onwards
- Progressive microgliosis and astrocytosis from an age of 10 months
- Cognitive impairment in the Morris water maze paradigm and hippocampal LTP deficit from an age of 6 months
- Early Aβ-induced GSK3-activation and mTAU phosphorylation in hippocampus and dystrophic neurites containing hyperphosphorylated mTau (no tangle-pathology)
- CAA pathology and micro-bleedings from an age of 15-18 and 25-30 months, respectively

Progressive total plaque load (an anti-Aβ antibody) and dense plaque load (Thioflavin S) in the subiculum as measured by IHC (mean ± SEM, N = 5-9).

The London mutation [V717] is a preferred model for anti-BACE1 approaches. The Swedish mutation might result in an aberrant subcellular localization of APP (Jacobsen et al., 2014).

Long term potentiation deficit (induced by a high frequency stimulation) in the CA1 region of the hippocampus in 8 month old APP[V717] animals and age-matched littermates can be restored with a therapeutic compound (mean ± SEM, n = 5 per group).
Literature
Describing papers:
- Original paper: Moechars et al., 1999: Early phenotypic changes in transgenic mice that overexpress different mutants of amyloid precursor protein in brain. DOI: 10.1074/jbc.274.10.6483
- Tanghe et al., 2010: Pathological Hallmarks, Clinical Parallels, and Value for Drug Testing in Alzheimer’s Disease of the APP[V717I] London Transgenic Mouse Model. DOI: 10.4061/2010/417314
- Van Dorpe et al., 2000: Prominent cerebral amyloid angiopathy in transgenic mice overexpressing the london mutant of human APP in neurons. DOI: 10.1016/S0002-9440(10)64644-5
- Terwel et al., 2008: Amyloid activates GSK-3beta to aggravate neuronal tauopathy in bigenic mice. DOI: 10.2353/ajpath.2008.070904
Therapeutic intervention papers:
- Jacobsen et al, 2014: Combined Treatment with a BACE Inhibitor and Anti-Aβ Antibody Gantenerumab Enhances Amyloid Reduction in APPLondon Mice. DOI: 10.1523/JNEUROSCI.1405-14.2014
- Janssens et al., 2021: Passive immunotherapy with a novel antibody against 3pE-modified Aβ demonstrates potential for enhanced efficacy and favorable safety in combination with BACE inhibitor treatment in plaque-depositing mice. DOI: 10.1016/j.nbd.2021.105365
Services
Don’t See Your Model? We Can Help!
Our experts specialize in tailored solutions to meet your unique research needs. Let’s discuss how we can support your project.
Elevate Your Research With Additional Services
Readouts & Analyses
- Full suite of histopathology services
- Immunohistochemistry of brain and nerve tissues (IHC)
- Bioanalyses in various biological matrices
- Flow Cytometry
- ELISA, Ultra-Sensitive ELISA for CSF/plasma biomarkers
- Meso Scale Discovery (MSD)
- Immunoblotting
In Vivo Analyses
- Mouse breeding and genotyping
- Microbiome transplantation studies
- Compound administration
- Stereotaxic surgery
- EEG, EMG and ECG analyses
- Cannula implantation
- Tissue collection and analysis
Stay Curious: More Articles to Explore
AAALAC Accreditation
InnoSer has earned the AAALAC accreditation, demonstrating our commitment to responsible animal care and use. AAALAC International is a nonprofit organization that promotes the humane treatment of animals in science through voluntary accreditation and assessment programs. Our accreditation is valid for three years, incl. 2023. Read more about the AAALAC accreditation programme here.
Animal Welfare
The 3Rs impact everything from policy and regulatory change to the development and uptake of new technologies and approaches. This is why InnoSer has ongoing commitment and monitoring of these processes. The steps we practice maximize our ability to replace, reduce and refine animal involvement and facilitate our commitment to these principles when it comes to research and drug development.
info@innoserlaboratories.com