Evidence map›Paper›PMID 29505781›Full record

Trial reportAnalytical biochemistry2018

Analyzing mitochondrial function in human peripheral blood mononuclear cells.

Chao-Pin Hsiao, Charles Hoppel

Abstract readClinical Trial
In one paragraph

Trial report in Analytical biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Sepsis-induced mitochondrial dysfunction: A narrative review.World journal of critical care medicine · 2023
    Review
  7. Article
  8. Article
  9. Host mitochondria: more than an organelle in SARS-CoV-2 infection.Frontiers in cellular and infection microbiology · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Differential Levels of Endoplasmic Reticulum Stress in Peripheral Blood Mononuclear Cells from Patients with Sudden Sensorineural Hearing Loss.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  17. Review
  18. Platelet Mitochondrial Respiration, Endogenous Coenzyme QDiagnostics (Basel, Switzerland) · 2020
    Article
  19. Review
  20. Relationships between expression ofCancer management and research · 2019
    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 1 institution in 1 country.

Chao-Pin HsiaoFrances Payne Bolton School of Nursing, Case Western Reserve University, USA. Electronic address: cxh416@case.edu.
Charles HoppelCenter for Mitochondrial Disease, Department of Pharmacology and Medicine, School of Medicine, Case Western Reserve University, USA.
Case Western Reserve University · US

Funding

Mitochondrial Bioenergetic Mechanism of Cancer Related FatigueK01NR015246 · NINR · CASE WESTERN RESERVE UNIVERSITY · PI HSIAO, CHAO-PIN · 2015 to 2017
$273k
NINR NIH HHS K01 NR015246
6 · The paper itself

Abstract

Mitochondrial oxidative phosphorylation (OXPHOS) is responsible for producing most of the adenosine triphosphate required by eukaryotic cells. Lymphocytes make up the majority of the peripheral blood mononuclear cells. Peripheral blood mononuclear cells are readily obtainable, providing an ideal sample to monitor systemic changes and understand molecular signaling mechanisms in disease processes. Mitochondrial energy metabolism of lymphocyte has been used to screen for OXPHOS disorders. While there are increasing studies of lymphocyte OXPHOS, few studies examined activity of electron transport chain of lymphocyte mitochondria. We present an optimal protocol to harvest fresh peripheral blood mononuclear cells from human whole blood, determine integrated mitochondrial function, and analyze electron transport chain complex activity. Analyzing integrated mitochondrial function using OXPHOS provides data to uncover defects in the transport of substrates into the mitochondria, generation of reducing equivalents, the electron transport chain, and coupling to the production of adenosine triphosphate. The optimal conditions to harvest peripheral blood mononuclear cells were using blood anticoagulated with ethylenediaminetetraacetic acid, processed utilizing Lymphoprep™, and washed in phosphate buffered saline, all at room temperature. Using isolated peripheral blood mononuclear cells, integrated mitochondrial function and the activities of electron transport chain were determined.

Indexed as

Oxidative PhosphorylationAgedElectron TransportElectron Transport Chain Complex ProteinsHumansLymphocytesMaleMiddle AgedMitochondriaElectron Transport Chain Complex ProteinsBioenergeticsElectron transport chain complex activityHuman lymphocyteIntegrated mitochondrial functionOxidative phosphorylationPeripheral blood mononuclear cells

Identifiers

PMID29505781
PMCPMC5938136
OpenAlexW2792690444

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.