Evidence map›Paper›PMID 40960450›Full record

ArticleAutophagy2025

Aggregate fragmentation: the ticket to aggrephagy.

Mario Mauthe, Harm Kampinga, Fulvio Reggiori

Abstract read
In one paragraph

Article in Autophagy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Human Hsp70 paralogs display selective J-domain interactions tuning proteostasis under stress.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Review
  3. Recent insights into HSP70: proteostasis and beyond.Frontiers in molecular biosciences · 2026
    Review
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

3 authors.

Mario MautheDepartment of Biomedical Sciences, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0003-0049-7961
Harm KampingaDepartment of Biomedical Sciences, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0002-8966-8466
Fulvio ReggioriDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0003-2652-2686

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our recent study identifies a previously unrecognized requirement for protein aggregate fragmentation as a prerequisite for autophagic clearance of amorphous aggregates, a process that has been termed aggrephagy. We show that aggregate fragmentation depends on two distinct but cooperative components: the DNAJB6 (DnaJ heat shock protein family (Hsp40) member B6)-HSPA/HSP70 (heat shock protein family A (Hsp70))-HSPH1/HSP110 chaperone module and the 19S regulatory particles (RPs) of the proteasome. These factors act together to not only to fragment protein aggregates but also to compact them, enabling clustering of selective autophagy receptors (SARs) and subsequent local phagophore formation. Our results show that this fragmentase activity plays a role in the aggrephagic clearance of different aggregate species, including disease-related HTT (huntingtin) aggregates.

Indexed as

AutophagyProtein AggregatesAnimalsHSP40 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsHumansMolecular ChaperonesProteasome Endopeptidase ComplexHSP40 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsMolecular ChaperonesProteasome Endopeptidase ComplexProtein AggregatesAmorphousamyloidchaperoneclusteringproteasomeselective autophagy receptors

Identifiers

PMID40960450
PMCPMC12758229

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.