Evidence map›Paper›PMID 35738078›Full record

ArticleColloids and surfaces. B, Biointerfaces2022

Molecular recognition between membrane epitopes and nearly free surface silanols explains silica membranolytic activity.

Cristina Pavan, Matthew J Sydor, Chiara Bellomo, Riccardo Leinardi, Stefania Cananà, Rebekah L Kendall, Erica Rebba, Marta Corno, Piero Ugliengo, Lorenzo Mino and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Colloids and surfaces. B, Biointerfaces, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

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  14. Top-Down Preparation of Nanoquartz for Toxicological Investigations.International journal of molecular sciences · 2022
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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

12 authors at 3 institutions in 3 countries.

Cristina PavanDepartment of Chemistry, University of Turin, Italy; "G. Scansetti" Interdepartmental Centre for Studies on Asbestos and Other Toxic Particulates, University of Turin, Italy; Louvain Centre for Toxicology and Applied Pharmacology, Université catholique de Louvain, Belgium. Electronic address: cristina.pavan@unito.it.
Matthew J SydorCenter for Environmental Health Sciences, Department of Biomedical and Pharmaceutical Sciences, University of Montana, Missoula, United States. Electronic address: matthew.sydor@umconnect.umt.edu.
Chiara BellomoDepartment of Chemistry, University of Turin, Italy; "G. Scansetti" Interdepartmental Centre for Studies on Asbestos and Other Toxic Particulates, University of Turin, Italy. Electronic address: chiara.bellomo@unito.it.
Riccardo LeinardiDepartment of Chemistry, University of Turin, Italy; "G. Scansetti" Interdepartmental Centre for Studies on Asbestos and Other Toxic Particulates, University of Turin, Italy; Louvain Centre for Toxicology and Applied Pharmacology, Université catholique de Louvain, Belgium. Electronic address: riccardo.leinardi@uclouvain.be.
Stefania CananàDepartment of Chemistry, University of Turin, Italy; "G. Scansetti" Interdepartmental Centre for Studies on Asbestos and Other Toxic Particulates, University of Turin, Italy. Electronic address: stefania.canana@unito.it.
Rebekah L KendallCenter for Environmental Health Sciences, Department of Biomedical and Pharmaceutical Sciences, University of Montana, Missoula, United States. Electronic address: becky.kendall@umconnect.umt.edu.
Erica RebbaDepartment of Chemistry, University of Turin, Italy; Nanostructured Interfaces and Surfaces Interdepartmental Centre, University of Turin, Italy. Electronic address: erica.rebba@unito.it.
Marta CornoDepartment of Chemistry, University of Turin, Italy; Nanostructured Interfaces and Surfaces Interdepartmental Centre, University of Turin, Italy. Electronic address: marta.corno@unito.it.
Piero UgliengoDepartment of Chemistry, University of Turin, Italy; Nanostructured Interfaces and Surfaces Interdepartmental Centre, University of Turin, Italy. Electronic address: piero.ugliengo@unito.it.
Lorenzo MinoDepartment of Chemistry, University of Turin, Italy; Nanostructured Interfaces and Surfaces Interdepartmental Centre, University of Turin, Italy. Electronic address: lorenzo.mino@unito.it.
Andrij HolianCenter for Environmental Health Sciences, Department of Biomedical and Pharmaceutical Sciences, University of Montana, Missoula, United States. Electronic address: andrij.holian@umontana.edu.
Francesco TurciDepartment of Chemistry, University of Turin, Italy; "G. Scansetti" Interdepartmental Centre for Studies on Asbestos and Other Toxic Particulates, University of Turin, Italy; Nanostructured Interfaces and Surfaces Interdepartmental Centre, University of Turin, Italy. Electronic address: francesco.turci@unito.it.
University of Turin · ITCenter for Environmental Health · USUCLouvain · BE

Funding

Surveillance genome sequencing to detect SARS-CoV-2 virus variants in MontanaP20GM103546 · NIGMS · UNIVERSITY OF MONTANA · PI BOWLER, BRUCE E · 2012 to 2021
$19.2M
Molecular Histology and Fluorescent ImagingP30GM103338 · NIGMS · UNIVERSITY OF MONTANA · PI HOLIAN, ANDRIJ · 2013 to 2017
$5.6M
Role of particle surface functionalization in inflammationR01ES033533 · NIEHS · UNIVERSITY OF MONTANA · PI Andrij Holian · 2022 to 2026
$2.7M
NIEHS NIH HHS R01 ES033533NIGMS NIH HHS P20 GM103546NIGMS NIH HHS P30 GM103338
6 · The paper itself

Abstract

Inhaled crystalline silica causes inflammatory lung diseases, but the mechanism for its unique activity compared to other oxides remains unclear, preventing the development of potential therapeutics. Here, the molecular recognition mechanism between membrane epitopes and "nearly free silanols" (NFS), a specific subgroup of surface silanols, is identified and proposed as a novel broad explanation for particle toxicity in general. Silica samples having different bulk and surface properties, specifically different amounts of NFS, are tested with a set of membrane systems of decreasing molecular complexity and different charge. The results demonstrate that NFS content is the primary determinant of membrane disruption causing red blood cell lysis and changes in lipid order in zwitterionic, but not in negatively charged liposomes. NFS-rich silica strongly and irreversibly adsorbs zwitterionic self-assembled phospholipid structures. This selective interaction is corroborated by density functional theory and supports the hypothesis that NFS recognize membrane epitopes that exhibit a positive quaternary amino and negative phosphate group. These new findings define a new paradigm for deciphering particle-biomembrane interactions that will support safer design of materials and what types of treatments might interrupt particle-biomembrane interactions.

Indexed as

SilanesSilicon DioxideEpitopesSurface PropertiesEpitopesSilanessilanolSilicon DioxideLiposomeMacrophageMembranePhospholipidQuartzSilica

Identifiers

PMID35738078
PMCPMC10796170
OpenAlexW4282827226

What OpenQuestion holds

Textmetadata
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.