Evidence map›Paper›PMID 26216973›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Single-cell measurement of red blood cell oxygen affinity.

Giuseppe Di Caprio, Chris Stokes, John M Higgins, Ethan Schonbrun

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03101215 (Workload of Water Polo Players Following a Phosphorus Manipulated High Carbohydrate Meal), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.3field-weighted citation impact, top 20% 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.

NCT03101215 naunknown statusnot on this mapstarted 2017, after this paper: background citation

Workload of Water Polo Players Following a Phosphorus Manipulated High Carbohydrate Meal

TypeinterventionalSponsorAmerican University of Beirut Medical CenterRan2017 to 2018Enrolled17ConditionsEnergy ExpenditureArmsphosphorus
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. High-throughput quantification of red blood cell deformability and oxygen saturation to probe mechanisms of sickle cell disease.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Article
  8. Article
  9. Phenotypic screening of the ReFRAME drug repurposing library to discover new drugs for treating sickle cell disease.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Article
  11. Specificity of Nuclear Size Scaling in Frog Erythrocytes.Frontiers in cell and developmental biology · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Remote ischemic conditioning enhances oxygen supply to ischemic brain tissue in a mouse model of stroke: Role of elevated 2,3-biphosphoglycerate in erythrocytes.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
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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

4 authors at 1 institution in 1 country.

Giuseppe Di CaprioThe Rowland Institute, Harvard University, Cambridge, MA 02142; dicaprio@rowland.harvard.edu.
Chris StokesThe Rowland Institute, Harvard University, Cambridge, MA 02142;
John M HigginsCenter for Systems Biology, Massachusetts General Hospital, Boston, MA 02115; Department of Systems Biology, Harvard Medical School, Boston, MA 02115.
Ethan SchonbrunThe Rowland Institute, Harvard University, Cambridge, MA 02142;
Harvard University · US

Funding

Multiscale Modeling of Sickle Cell Anemia: Methods and ValidationU01HL114476 · NHLBI · BROWN UNIVERSITY · PI DAO, MING, HIGGINS, JOHN MATTHEW · 2013 to 2017
$3.9M
Systems Biology of In Vivo Human Blood Cell PopulationsDP2DK098087 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI HIGGINS, JOHN MATTHEW · 2012 to 2012
$2.6M
NHLBI NIH HHS U01 HL114476NIDDK NIH HHS DP2 DK098087
6 · The paper itself

Abstract

Oxygen is transported throughout the body by hemoglobin (Hb) in red blood cells (RBCs). Although the oxygen affinity of blood is well-understood and routinely assessed in patients by pulse oximetry, variability at the single-cell level has not been previously measured. In contrast, single-cell measurements of RBC volume and Hb concentration are taken millions of times per day by clinical hematology analyzers, and they are important factors in determining the health of the hematologic system. To better understand the variability and determinants of oxygen affinity on a cellular level, we have developed a system that quantifies the oxygen saturation, cell volume, and Hb concentration for individual RBCs in high throughput. We find that the variability in single-cell saturation peaks at an oxygen partial pressure of 2.9%, which corresponds to the maximum slope of the oxygen-Hb dissociation curve. In addition, single-cell oxygen affinity is positively correlated with Hb concentration but independent of osmolarity, which suggests variation in the Hb to 2,3-diphosphoglycerate (2-3 DPG) ratio on a cellular level. By quantifying the functional behavior of a cellular population, our system adds a dimension to blood cell analysis and other measurements of single-cell variability.

Indexed as

ErythrocytesFlow CytometryHemoglobinsHumansKineticsOxygenSingle-Cell AnalysisSpectrum AnalysisHemoglobinsOxygenflow cytometryhematologymedical sciencesorgan on chipsingle-cell variability

Identifiers

PMID26216973
PMCPMC4538663
OpenAlexW2139403988

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.