Evidence map›Paper›PMID 26445788›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2015

Flow Cytometric Analysis of Immune Cells Within Murine Aorta.

Breanne N Gjurich, Parésa L Taghavie-Moghadam, Elena V Galkina

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.3field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Survey of Approaches for Investigation of Atherosclerosis In Vivo.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  9. Article
  10. Article
  11. Extracellular vesicles derived from injured vascular tissue promote the formation of tertiary lymphoid structures in vascular allografts.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    Article
  12. Article
  13. Article
  14. Hepcidin Deficiency Protects Against Atherosclerosis.Arteriosclerosis, thrombosis, and vascular biology · 2019
    Article
  15. Atherosclerosis in the single-cell era.Current opinion in lipidology · 2018
    Review
  16. Article
  17. Article
  18. Article
  19. Identification of heterogeneous subsets of aortic interleukin-17A-expressing CD4International journal of immunopathology and pharmacology
    Article
  20. 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

3 authors at 1 institution in 1 country.

Breanne N GjurichDepartment of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, 700 West Olney Road, Norfolk, VA, 23507-1696, USA.
Parésa L Taghavie-MoghadamDepartment of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, 700 West Olney Road, Norfolk, VA, 23507-1696, USA.
Elena V GalkinaDepartment of Microbiology and Molecular Cell Biology, Eastern Virginia Medical School, 700 West Olney Road, Norfolk, VA, 23507-1696, USA. galkinev@evms.edu.
Eastern Virginia Medical School · US

Funding

Role of the Interleukin12/STAT4 Pathway in Insulin Resistance and AtherosclerosisR01HL112605 · NHLBI · EASTERN VIRGINIA MEDICAL SCHOOL · PI NADLER, JERRY L. · 2012 to 2016
$2.0M
T cell plasticity in atherosclerosisR01HL107522 · NHLBI · EASTERN VIRGINIA MEDICAL SCHOOL · PI GALKINA, ELENA V · 2011 to 2015
$1.8M
NHLBI NIH HHS HL112605 02S1NHLBI NIH HHS R01 HL107522NHLBI NIH HHS R01HL107522NHLBI NIH HHS R01 HL112605
6 · The paper itself

Abstract

The immune system plays a critical role in the modulation of atherogenesis at all stages of the disease. However, there are many technical difficulties when studying the immune system within murine aortas. Common techniques such as PCR and immunohistochemistry have answered many questions about the presence of immune cells and mediators of inflammation within the aorta yet many questions remain unanswered due to the limitations of these techniques. On the other hand, cumulatively the flow cytometry approach has propelled the immunology field forward but it has been challenging to apply this technique to aortic tissues. Here, we describe the methodology to isolate and characterize the immune cells within the murine aorta and provide examples of functional assays for aortic leukocytes using flow cytometry. The method involves the harvesting and enzymatic digestion of the aorta, extracellular and intracellular protein staining, and a subsequent flow cytometric analysis.

Indexed as

Flow CytometryAnimalsAortaAortic DiseasesAtherosclerosisBiomarkersCell SeparationDisease Models, AnimalImmunophenotypingLeukocytesMicePhenotypeBiomarkersAtherosclerosisFlow cytometryLeukocytesMouse aorta

Identifiers

PMID26445788
PMCPMC4638413
OpenAlexW2409864713

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.