Evidence map›Paper›PMID 25967951›Full record

ArticleJournal of immunological methods2015

Uncovering Leishmania-macrophage interplay using imaging flow cytometry.

Cesar Terrazas, Steve Oghumu, Sanjay Varikuti, Diana Martinez-Saucedo, Stephen M Beverley, Abhay R Satoskar

Abstract read
In one paragraph

Article in Journal of immunological methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Overcharged lipid metabolism in mechanisms of antitumor byInternational journal of oncology · 2023
    Article
  5. Frontiers in cellular and infection microbiology · 2022
    Article
  6. The balancing act: Immunology of leishmaniosis.Research in veterinary science · 2020
    Review
  7. Article
  8. Article
  9. Injection of T3SS effectors not resulting in invasion is the main targeting mechanism ofProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  10. Review
  11. IL-17A promotes susceptibility during experimental visceral leishmaniasis caused by Leishmania donovani.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2016
    Article
  12. Review
  13. 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

6 authors at 2 institutions in 1 country.

Cesar TerrazasDepartment of Pathology, Ohio State University Medical Center, Columbus, OH, USA. Electronic address: cterrazas.05@gmail.com.
Steve OghumuDepartment of Pathology, Ohio State University Medical Center, Columbus, OH, USA.
Sanjay VarikutiDepartment of Pathology, Ohio State University Medical Center, Columbus, OH, USA.
Diana Martinez-SaucedoDepartment of Pathology, Ohio State University Medical Center, Columbus, OH, USA; UBIMED, FES-Iztacala, UNAM, Tlalnepantla Estado de Mexico, Mexico.
Stephen M BeverleyDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Abhay R SatoskarDepartment of Pathology, Ohio State University Medical Center, Columbus, OH, USA. Electronic address: abhay.satoskar@osumc.edu.
The Ohio State University · USWashington University in St. Louis · US

Funding

MOLECULAR GENETICS OF LEISHMANIA USING DNA TRANSFECTIONR01AI029646 · NIAID · WASHINGTON UNIVERSITY · PI BEVERLEY, STEPHEN M · 1990 to 2015
$9.3M
NIAID NIH HHS NIH AI29646NIAID NIH HHS R01 AI029646
6 · The paper itself

Abstract

Host-pathogen interaction is an area of considerable interest. Intracellular parasites such as Leishmania reside inside phagocytes such as macrophages, dendritic cells and neutrophils. Macrophages can be activated by cytokines such as IFN-γ and Toll like receptor (TLR) agonists resulting in enhanced microbicidal activity. Leishmania parasites hijack the microbicidal function of macrophages, mainly by interfering with intracellular signaling initiated by IFN-γ and TLR ligands. Here we used transgenic Leishmania donovani parasites expressing the red fluorescent protein DsRed2 and imaging-flow cytometry technology to evaluate parasitic loads inside the macrophage in vitro. Further, this methodology enables us to visualize impairment in NFκB translocation to the nucleus in L. donovani infected macrophages. Additionally we show that uninfected bystander macrophages have a similar impairment in NFκB translocation as in L. donovani infected macrophages in response to the TLR4 agonist LPS. This evidence suggests a possible immunosuppressive role for infected macrophages in regulating the activation of uninfected bystander macrophages.

Indexed as

AnimalsFlow CytometryHost-Pathogen InteractionsImage CytometryInterferon-gammaLeishmania donovaniLeishmaniasis, VisceralLigandsLuminescent ProteinsMacrophage ActivationMacrophagesMiceMice, Inbred BALB CNF-kappa BRed Fluorescent ProteinSignal TransductionInterferon-gammaLigandsLuminescent ProteinsNF-kappa BRed Fluorescent ProteinToll-Like Receptor 4AutomatedFlow cytometryImagingIntracellular signalingLeishmaniaMacrophages

Identifiers

PMID25967951
PMCPMC4620550
OpenAlexW319178438

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.