Evidence map›Paper›PMID 32510331›Full record

ArticleeLife2020

Fibrillar Aβ triggers microglial proteome alterations and dysfunction in Alzheimer mouse models.

Laura Sebastian Monasor, Stephan A Müller, Alessio Vittorio Colombo, Gaye Tanrioever, Jasmin König, Stefan Roth, Arthur Liesz, Anna Berghofer, Anke Piechotta, Matthias Prestel and 7 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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

96 citing papers in PubMed, 1 synthesis or guideline pooled it, 138 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. ApoE lipidation state directs immunometabolic reprogramming of human microglia.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
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36 more citing papers are in PubMed but not listed here.

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 6 institutions in 2 countries.

Laura Sebastian Monasor *German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.ORCID 0000-0001-7864-7400
Stephan A Müller *German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.ORCID 0000-0003-3414-307X
Alessio Vittorio ColomboGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Gaye TanrioeverGerman Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
Jasmin KönigGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Stefan RothInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU, Munich, Germany.
Arthur LieszInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU, Munich, Germany.
Anna BerghoferNeuroproteomics, School of Medicine, Klinikum Rechts der Isar, Technical University, Munich, Germany.
Anke PiechottaDepartment of Molecular Drug Design and Target Validation, Fraunhofer Institute for Cell Therapy and Immunology, Halle, Germany.
Matthias PrestelInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU, Munich, Germany.
Takashi SaitoLaboratory for Proteolytic Neuroscience, RIKEN Center for Brain Science Institute, Wako, Japan.
Takaomi C SaidoLaboratory for Proteolytic Neuroscience, RIKEN Center for Brain Science Institute, Wako, Japan.
Jochen HermsGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Michael WillemBiomedical Center (BMC), Ludwig-Maximilians Universität München, Munich, Germany.
Christian HaassGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Stefan F LichtenthalerGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.ORCID 0000-0003-2211-2575
Sabina TahirovicGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.ORCID 0000-0003-4403-9559
German Center for Neurodegenerative Diseases · DELMU Klinikum · DERIKEN Center for Brain Science · JPFraunhofer Institute for Cell Therapy and Immunology · DELudwig-Maximilians-Universität München · DETUM Klinikum · DE

Funding

Alzheimer Forschung Initiative 18014Bundesministerium für Bildung und Forschung CLINSPECT-MBundesministerium für Bildung und Forschung JPND PMG-ADDeutsche Forschungsgemeinschaft EXC 2145 SyNergy ID 390857198Deutsche Forschungsgemeinschaft Koselleck Project HA1737/16-1H2020 European Research Council ERC-StG 802305Helmholtz-Gemeinschaft ZT-0027NCL Foundation 01133
6 · The paper itself

Abstract

Microglial dysfunction is a key pathological feature of Alzheimer's disease (AD), but little is known about proteome-wide changes in microglia during the course of AD and their functional consequences. Here, we performed an in-depth and time-resolved proteomic characterization of microglia in two mouse models of amyloid β (Aβ) pathology, the overexpression APPPS1 and the knock-in APP-NL-G-F (APP-KI) model. We identified a large panel of Microglial Aβ Response Proteins (MARPs) that reflect heterogeneity of microglial alterations during early, middle and advanced stages of Aβ deposition and occur earlier in the APPPS1 mice. Strikingly, the kinetic differences in proteomic profiles correlated with the presence of fibrillar Aβ, rather than dystrophic neurites, suggesting that fibrillar Aβ may trigger the AD-associated microglial phenotype and the observed functional decline. The identified microglial proteomic fingerprints of AD provide a valuable resource for functional studies of novel molecular targets and potential biomarkers for monitoring AD progression or therapeutic efficacy.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAnimalsDisease Models, AnimalFemaleGene Knock-In TechniquesMaleMiceMice, TransgenicMicrogliaProteomeAmyloid beta-PeptidesAmyloid beta-Protein PrecursorProteomeAlzheimer's diseasemicrogliamouseneuroinflammationneurosciencephagocytosisproteomic signatures

Identifiers

PMID32510331
PMCPMC7279888
OpenAlexW3034168187

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.