Evidence map›Paper›PMID 30200270›Full record

ArticleInternational journal of molecular sciences2018

Identification of Oxidative Stress in Red Blood Cells with Nanoscale Chemical Resolution by Infrared Nanospectroscopy.

Francesco S Ruggeri, Curtis Marcott, Simone Dinarelli, Giovanni Longo, Marco Girasole, Giovanni Dietler, Tuomas P J Knowles

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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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

7 authors.

Francesco S RuggeriDepartment of Chemistry, Cambridge University, Cambridge CB21EW, UK. fsr26@cam.ac.uk.ORCID 0000-0002-1232-1907
Curtis MarcottDepartment of Materials Science and Engineering, University of Delaware, Newark, DE 19716, USA. marcott@lightlightsolutions.com.
Simone DinarelliInstitute of Structural Matter, ISM-CNR, via del Fosso del Cavaliere 100, 00133 Rome, Italy. simone.dinarelli@artov.ism.cnr.it.ORCID 0000-0002-9172-4973
Giovanni LongoInstitute of Structural Matter, ISM-CNR, via del Fosso del Cavaliere 100, 00133 Rome, Italy. longo@ism.cnr.it.ORCID 0000-0003-2434-2155
Marco GirasoleInstitute of Structural Matter, ISM-CNR, via del Fosso del Cavaliere 100, 00133 Rome, Italy. girasole@ism.cnr.it.
Giovanni DietlerLaboratoire de Physique de la Matière Vivante, Ecole Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland. giovanni.dietler@epfl.ch.
Tuomas P J KnowlesDepartment of Chemistry, Cambridge University, Cambridge CB21EW, UK. tpjk2@cam.ac.uk.

Funding

European Research Council PhysProt 337969Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 152958, P300P2_171219, and 200021_162767
6 · The paper itself

Abstract

During their lifespan, Red blood cells (RBC), due to their inability to self-replicate, undergo an ageing degradation phenomenon. This pathway, both in vitro and in vivo, consists of a series of chemical and morphological modifications, which include deviation from the biconcave cellular shape, oxidative stress, membrane peroxidation, lipid content decrease and uncoupling of the membrane-skeleton from the lipid bilayer. Here, we use the capabilities of atomic force microscopy based infrared nanospectroscopy (AFM-IR) to study and correlate, with nanoscale resolution, the morphological and chemical modifications that occur during the natural degradation of RBCs at the subcellular level. By using the tip of an AFM to detect the photothermal expansion of RBCs, it is possible to obtain nearly two orders of magnitude higher spatial resolution IR spectra, and absorbance images than can be obtained on diffraction-limited commercial Fourier-transform Infrared (FT-IR) microscopes. Using this approach, we demonstrate that we can identify localized sites of oxidative stress and membrane peroxidation on individual RBC, before the occurrence of neat morphological changes in the cellular shape.

Indexed as

Oxidative StressCell ShapeErythrocyte CountErythrocytesHumansLipid PeroxidationMembrane LipidsMicroscopy, Atomic ForceNanotechnologySpectrophotometry, InfraredMembrane Lipidsatomic force microscopyinfrared nanospectroscopymembrane peroxidationoxidative stressred blood cells

Identifiers

PMID30200270
PMCPMC6163177

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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.