Evidence map›Paper›PMID 35008451›Full record

ArticleInternational journal of molecular sciences2021

The Dynamics of β-Amyloid Proteoforms Accumulation in the Brain of a 5xFAD Mouse Model of Alzheimer's Disease.

Anna E Bugrova, Polina A Strelnikova, Maria I Indeykina, Alexey S Kononikhin, Natalia V Zakharova, Alexander G Brzhozovskiy, Evgeny P Barykin, Stanislav I Pekov, Maria S Gavrish, Alexey A Babaev and 7 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 1 country.

Anna E BugrovaEmanuel Institute of Biochemical Physics, Russian Academy of Science, 119334 Moscow, Russia.ORCID 0000-0003-1515-9447
Polina A StrelnikovaEmanuel Institute of Biochemical Physics, Russian Academy of Science, 119334 Moscow, Russia.ORCID 0000-0001-6513-8009
Maria I IndeykinaEmanuel Institute of Biochemical Physics, Russian Academy of Science, 119334 Moscow, Russia.ORCID 0000-0002-8177-7449
Alexey S KononikhinEngelhardt Institute of Molecular Biology, Russian Academy of Science, 119991 Moscow, Russia.ORCID 0000-0002-2238-3458
Natalia V ZakharovaEmanuel Institute of Biochemical Physics, Russian Academy of Science, 119334 Moscow, Russia.
Alexander G BrzhozovskiySkolkovo Institute of Science and Technology, 121205 Moscow, Russia.
Evgeny P BarykinEngelhardt Institute of Molecular Biology, Russian Academy of Science, 119991 Moscow, Russia.
Stanislav I PekovMoscow Institute of Physics and Technology, 141701 Dolgoprudny, Russia.ORCID 0000-0002-9622-3457
Maria S GavrishInstitute of Neuroscience, Lobachevsky State University of Nizhny Novgorod, 603022 Nizhny Novgorod, Russia.
Alexey A BabaevInstitute of Neuroscience, Lobachevsky State University of Nizhny Novgorod, 603022 Nizhny Novgorod, Russia.
Anna M KosyrevaResearch Institute of Human Morphology, 117418 Moscow, Russia.ORCID 0000-0002-6182-1799
Anna Y MorozovaDepartment of Basic and Applied Neurobiology, Federal Medical Research Center for Psychiatry and Narcology, 119034 Moscow, Russia.
Daniil A DegterevEngelhardt Institute of Molecular Biology, Russian Academy of Science, 119991 Moscow, Russia.
Vladimir A MitkevichEngelhardt Institute of Molecular Biology, Russian Academy of Science, 119991 Moscow, Russia.ORCID 0000-0002-1517-1983
Igor A PopovMoscow Institute of Physics and Technology, 141701 Dolgoprudny, Russia.
Alexander A MakarovEngelhardt Institute of Molecular Biology, Russian Academy of Science, 119991 Moscow, Russia.
Evgeny N NikolaevSkolkovo Institute of Science and Technology, 121205 Moscow, Russia.
Engelhardt Institute of Molecular Biology · RUInstitute of Biochemical Physics NM Emanuel · RUMoscow Institute of Physics and Technology · RUN. I. Lobachevsky State University of Nizhny Novgorod · RUSkolkovo Institute of Science and Technology · RUMoscow Research and Clinical Center for Neuropsychiatry · RUResearch Institute of Human Morphology · RU

Funding

Ministry of Science and Higher Education of the Russian Federation grant agreement № 075-15-2020-795, state contract № 13.1902.21.0027 of 29.09.2020 unique project ID: RF-190220X0027
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the leading cause of dementia among the elderly. Neuropathologically, AD is characterized by the deposition of a 39- to 42-amino acid long β-amyloid (Aβ) peptide in the form of senile plaques. Several post-translational modifications (PTMs) in the N-terminal domain have been shown to increase the aggregation and cytotoxicity of Aβ, and specific Aβ proteoforms (e.g., Aβ with isomerized D7 (isoD7-Aβ)) are abundant in the senile plaques of AD patients. Animal models are indispensable tools for the study of disease pathogenesis, as well as preclinical testing. In the presented work, the accumulation dynamics of Aβ proteoforms in the brain of one of the most widely used amyloid-based mouse models (the 5xFAD line) was monitored. Mass spectrometry (MS) approaches, based on ion mobility separation and the characteristic fragment ion formation, were applied. The results indicated a gradual increase in the Aβ fraction of isoD7-Aβ, starting from approximately 8% at 7 months to approximately 30% by 23 months of age. Other specific PTMs, in particular, pyroglutamylation, deamidation, and oxidation, as well as phosphorylation, were also monitored. The results for mice of different ages demonstrated that the accumulation of Aβ proteoforms correlate with the formation of Aβ deposits. Although the mouse model cannot be a complete analogue of the processes occurring in the human brain in AD, and several of the observed parameters differ significantly from human values supposedly due to the limited lifespan of the model animals, this dynamic study provides evidence on at least one of the possible mechanisms that can trigger amyloidosis in AD, i.e., the hypothesis on the relationship between the accumulation of isoD7-Aβ and the progression of AD-like pathology.

Indexed as

Alzheimer DiseaseAmyloidAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAnimalsBrainDisease Models, AnimalHumansMiceMice, TransgenicPhosphorylationPlaque, AmyloidAmyloidAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAlzheimer’s diseaseisoD7isoformsmass spectrometrymouse brainpost-translational modifications (PTM)proteoformsproteomicssenile plaquesβ-amyloid

Identifiers

PMID35008451
PMCPMC8745018
OpenAlexW4200480332

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.