Evidence map›Paper›PMID 26863129›Full record

ArticleJournal of visualized experiments : JoVE2016

Isolation of Infiltrating Leukocytes from Mouse Skin Using Enzymatic Digest and Gradient Separation.

Charles J Benck, Tijana Martinov, Brian T Fife, Devavani Chatterjea

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Research advances of tissue-derived extracellular vesicles in cancers.Journal of cancer research and clinical oncology · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. A long noncoding RNA regulates inflammation resolution by mouse macrophages through fatty acid oxidation activation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Protective immunity in recurrentProceedings of the National Academy of Sciences of the United States of America · 2018
    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

4 authors.

Charles J BenckDepartment of Biology, Macalester College.
Tijana MartinovDepartment of Medicine, Division of Rheumatic and Autoimmune Diseases, Center for Immunology, University of Minnesota.
Brian T FifeDepartment of Medicine, Division of Rheumatic and Autoimmune Diseases, Center for Immunology, University of Minnesota.
Devavani ChatterjeaDepartment of Biology, Macalester College; chatterjead@macalester.edu.

Funding

Contributions of mast cells to intersections of allergy and pain pathwaysR15AI113620 · NIAID · MACALESTER COLLEGE · PI CHATTERJEA, DEVAVANI · 2015 to 2016
$452k
Roles of Mast Cells in Inflammatory PainR15NS067536 · NINDS · MACALESTER COLLEGE · PI CHATTERJEA, DEVAVANI · 2010 to 2010
$426k
NIAID NIH HHS R15 AI113620NINDS NIH HHS R15 NS067536NINDS NIH HHS R15 NS067536-01A1
6 · The paper itself

Abstract

Dissociating murine skin into a single cell suspension is essential for downstream cellular analysis such as the characterization of infiltrating immune cells in rodent models of skin inflammation. Here, we describe a protocol for the digestion of mouse skin in a nutrient-rich solution with collagenase D, followed by separation of hematopoietic cells using a discontinuous density gradient. Cells thus obtained can be used for in vitro studies, in vivo transfer, and other downstream cellular and molecular analyses including flow cytometry. This protocol is an effective and economical alternative to expensive mechanical dissociators, specialized separation columns, and harsher trypsin- and dispase-based digestion methods, which may compromise cellular viability or density of surface proteins relevant for phenotypic characterization or cellular function. As shown here in our representative data, this protocol produced highly viable cells, contained specific immune cell subsets, and had no effect on integrity of common surface marker proteins used in flow cytometric analysis.

Indexed as

AllergensAnimalsCollagenasesFemaleFlow CytometryLeukocytesMiceNeutrophilsSkinT-LymphocytesAllergensCollagenases

Identifiers

PMID26863129
PMCPMC4781699

What OpenQuestion holds

Textmetadata
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.