Evidence map›Paper›PMID 32579964›Full record

ArticleBiophysical journal2020

The Amphipathic GM1 Molecule Stabilizes Amyloid Aggregates, Preventing their Cytotoxicity.

Monica Bucciantini, Manuela Leri, Massimo Stefani, Ronald Melki, Sandra Zecchi-Orlandini, Daniele Nosi

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Free Gangliosides Can Alter Amyloid-β Aggregation.The journal of physical chemistry letters · 2022
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
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

6 authors at 2 institutions in 2 countries.

Monica BucciantiniDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio," University of Florence, Florence, Italy. Electronic address: monica.bucciantini@unifi.it.
Manuela LeriDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio," University of Florence, Florence, Italy; Department of Neuroscience, Psychology, Area of Medicine and Health of the Child of the University of Florence, Florence, Italy.
Massimo StefaniDepartment of Experimental and Clinical Biomedical Sciences "Mario Serio," University of Florence, Florence, Italy.
Ronald MelkiInstitut Francois Jacob, CEA and Laboratory of Neurodegenerative Diseases, CNRS 92265, Fontenay-Aux-Roses, France.
Sandra Zecchi-OrlandiniDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
Daniele NosiDepartment of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
University of Florence · ITCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyloid aggregates have been demonstrated to exert cytotoxic effects in several diseases. It is widely accepted that the complex and fascinating aggregation pathway involves a series of steps during which many heterogeneous intermediates are generated. This process may be greatly potentiated by the presence of amphipathic components of plasma membrane because they may serve as interaction, condensation, and nucleation points. However, there are few data regarding structural alterations induced by the binding between the amyloid fibrils and membrane components and its direct effects on cell integrity. In this study, we found, by 1-anilinonaphthalene 8-sulfonic acid and transmission electron microscopy/fast Fourier transform, that yeast prion Sup35 oligomers showed higher structural uniformity and altered surface properties when grown in the presence of monosialotetrahexosylganglioside, a component of the cell membrane. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and confocal/sensitized Förster resonance energy transfer analyses revealed that these fibrils showed low cytotoxicity and affinity to plasma membrane. Moreover, time-lapse analysis of Sup35 oligomer fibrillation on cells suggested that the amyloid aggregation process per se exerts cytotoxic effects through the interaction of amyloid intermediates with plasma membrane components. These data provide, to our knowledge, new insights to understand the mechanism of amyloid growth and cytotoxicity in the pathogenesis of amyloid diseases.

Indexed as

AmyloidSaccharomyces cerevisiae ProteinsCell MembraneG(M1) GangliosidePeptide Termination FactorsSaccharomyces cerevisiaeAmyloidG(M1) GangliosidePeptide Termination FactorsSaccharomyces cerevisiae ProteinsSUP35 protein, S cerevisiae

Identifiers

PMID32579964
PMCPMC7376221
OpenAlexW3034460356

What OpenQuestion holds

Textmetadata
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.