Evidence map›Paper›PMID 24862269›Full record

ArticleMethods in enzymology2014

Use of chemical probes to detect mitochondrial ROS by flow cytometry and spectrofluorometry.

Jing Chen, Clayton E Mathews

Abstract read
In one paragraph

Article in Methods in enzymology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Type 1 Diabetes-Resistance LocusJournal of immunology (Baltimore, Md. : 1950) · 2017
    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

2 authors at 2 institutions in 1 country.

Jing ChenDepartment of Pathology, Immunology and Laboratory Medicine, The University of Florida College of Medicine, Gainesville, Florida, USA.
Clayton E MathewsDepartment of Pathology, Immunology and Laboratory Medicine, The University of Florida College of Medicine, Gainesville, Florida, USA. Electronic address: clayton.mathews@pathology.ufl.edu.
Florida College · USUniversity of Florida · US

Funding

Project 3P01AI042288 · NIAID · UNIVERSITY OF FLORIDA · PI Todd Michael Brusko · 1997 to 2026
$32.9M
Humoral And Cellular Tolerization Approaches Against AutoimmunityU19AI056374 · NIAID · CHILDREN'S HOSP PITTSBURGH/UPMC HLTH SYS · PI TRUCCO, MASSIMO M. · 2003 to 2007
$3.3M
Genetic Regulation of Human Beta Cell DestructionUC4DK104194 · NIDDK · UNIVERSITY OF FLORIDA · PI MATHEWS, CLAYTON E · 2014 to 2014
$3.1M
mt-Nd2 and Resistance to Autoimmune DiabetesR01DK074656 · NIDDK · UNIVERSITY OF FLORIDA · PI MATHEWS, CLAYTON E · 2006 to 2015
$2.8M
Regulatory Networks and Biomarkers of Beta-cell Dysfunction and ApoptosisUC4DK104167 · NIDDK · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI KULKARNI, ROHIT N., MATHEWS, CLAYTON E · 2014 to 2016
$2.7M
mt-Nd2 and resistance to autoimmune diabetesR56DK074656 · NIDDK · UNIVERSITY OF FLORIDA · PI MATHEWS, CLAYTON E · 2011 to 2011
$107k
NIAID NIH HHS AI056374NIAID NIH HHS AI42288NIAID NIH HHS P01 AI042288NIAID NIH HHS U19 AI056374NIDDK NIH HHS DK074656NIDDK NIH HHS R01 DK074656NIDDK NIH HHS R56 DK074656NIDDK NIH HHS UC4 DK104167NIDDK NIH HHS UC4 DK104194
6 · The paper itself

Abstract

Aerobic respiration is a major source of energy in eukaryotic cells. In this setting, ATP production by the mitochondrial respiratory chain relies on the availability of NADH and FADH2 to donate protons and electrons. The flux of electrons down the electron transport chain, based on a series of oxidation-reduction reactions, releases energy that allow for the transport of H(+) ions across the inner mitochondrial membrane. The resulting proton-motive force is employed to drive ATP synthesis, while the final acceptor of the electrons flowing through the respiratory chain if molecular oxygen. A side effect of this process is the generation of reactive oxygen species (ROS). While mitochondrial ROS (mtROS) production has been linked to many pathological conditions (i.e., aging and tumorigenesis), recent evidence suggests that multiple cells, including malignant cells, employ these by-products of energy production as signals to control various cellular processes. Here, we describe protocols to use chemical probes for measuring mtROS production in intact cells by flow cytometry and spectrofluorometry.

Indexed as

AnimalsApoptosisFlow CytometryHumansIndicators and ReagentsMitochondriaNeoplasmsOxidation-ReductionReactive Oxygen SpeciesSignal TransductionSpectrometry, FluorescenceIndicators and ReagentsReactive Oxygen SpeciesFluorescent dyesHydrogen peroxideHypoxiaOXPHOSRespiratory chainSuperoxide anion

Identifiers

PMID24862269
PMCPMC6421068
OpenAlexW2405109462

What OpenQuestion holds

Textmetadata
LicenceTDM
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.