Evidence map›Paper›PMID 25950144›Full record

ArticleScientific reports2015

Single-cell evaluation of red blood cell bio-mechanical and nano-structural alterations upon chemically induced oxidative stress.

Ameya Sinha, Trang T T Chu, Ming Dao, Rajesh Chandramohanadas

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing 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

45 citing papers in PubMed.

  1. Trial
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  15. Biophysical Tools and Concepts Enable Understanding of Asexual Blood Stage Malaria.Frontiers in cellular and infection microbiology · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Lab on a chip · 2021
    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

4 authors.

Ameya Sinha1] Engineering Product Development (EPD) Pillar, Singapore University of Technology &Design (SUTD), Singapore [2] Interdisciplinary Research Group of Infectious Diseases, Singapore MIT Alliance for Research &Technology Centre (SMART), Singapore.
Trang T T ChuEngineering Product Development (EPD) Pillar, Singapore University of Technology &Design (SUTD), Singapore.
Ming Dao1] Interdisciplinary Research Group of Infectious Diseases, Singapore MIT Alliance for Research &Technology Centre (SMART), Singapore [2] Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge-Massachusetts, U.S.A.
Rajesh ChandramohanadasEngineering Product Development (EPD) Pillar, Singapore University of Technology &Design (SUTD), Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erythroid cells, specifically red blood cells (RBCs), are constantly exposed to highly reactive radicals during cellular gaseous exchange. Such exposure often exceeds the cells' innate anti-oxidant defense systems, leading to progressive damage and eventual senescence. One of the contributing factors to this process are alterations to hemoglobin conformation and globin binding to red cell cytoskeleton. However, in addition to the aforementioned changes, it is possible that oxidative damage induces critical changes to the erythrocyte cytoskeleton and corresponding bio-mechanical and nano-structural properties of the red cell membrane. To quantitatively characterize how oxidative damage accounts for such changes, we employed single-cell manipulation techniques such as micropipette aspiration and atomic force microscopy (AFM) on RBCs. These investigations demonstrated visible morphological changes upon chemically induced oxidative damage (using hydrogen peroxide, diamide, primaquine bisphosphate and cumene hydroperoxide). Our results provide previously unavailable observations on remarkable changes in red cell cytoskeletal architecture and membrane stiffness due to oxidative damage. Furthermore, we also demonstrate that a pathogen that infects human blood cells, Plasmodium falciparum was unable to penetrate through the oxidant-exposed RBCs that have damaged cytoskeleton and stiffer membranes. This indicates the importance of bio-physical factors pertinent to aged RBCs and it's relevance to malaria infectivity.

Indexed as

Oxidation-ReductionSingle-Cell AnalysisErythrocyte DeformabilityErythrocyte MembraneErythrocytesHumansOxidantsOxidative StressPlasmodiumOxidants

Identifiers

PMID25950144
PMCPMC4423428

What OpenQuestion holds

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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.