Evidence map›Paper›PMID 27521343›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

A Csf1r-EGFP Transgene Provides a Novel Marker for Monocyte Subsets in Sheep.

Clare Pridans, Gemma M Davis, Kristin A Sauter, Zofia M Lisowski, Yolanda Corripio-Miyar, Anna Raper, Lucas Lefevre, Rachel Young, Mary E McCulloch, Simon Lillico and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Transcriptomic Analysis of Rat Macrophages.Frontiers in immunology · 2020
    Article
  4. Article
  5. Article
  6. Journal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  7. Article
  8. 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

13 authors at 1 institution in 1 country.

Clare PridansThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.ORCID 0000-0001-9423-557X
Gemma M DavisThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.ORCID 0000-0001-8323-5013
Kristin A SauterThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.
Zofia M LisowskiThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.
Yolanda Corripio-MiyarThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.ORCID 0000-0002-1344-7405
Anna RaperThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.
Lucas LefevreThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.
Rachel YoungThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.
Mary E McCullochThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.
Simon LillicoThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.ORCID 0000-0002-5101-2277
Elspeth MilneRoyal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian EH25 9RG, United Kingdom.
Bruce WhitelawThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and.ORCID 0000-0002-2918-1605
David A HumeThe Roslin Institute, University of Edinburgh, Midlothian EH25 9RG, United Kingdom; and David.Hume@roslin.ed.ac.uk.
Roslin Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L001209/1
6 · The paper itself

Abstract

Expression of Csf1r in adults is restricted to cells of the macrophage lineage. Transgenic reporters based upon the Csf1r locus require inclusion of the highly conserved Fms-intronic regulatory element for expression. We have created Csf1r-EGFP transgenic sheep via lentiviral transgenesis of a construct containing elements of the mouse Fms-intronic regulatory element and Csf1r promoter. Committed bone marrow macrophage precursors and blood monocytes express EGFP in these animals. Sheep monocytes were divided into three populations, similar to classical, intermediate, and nonclassical monocytes in humans, based upon CD14 and CD16 expression. All expressed EGFP, with increased levels in the nonclassical subset. Because Csf1r expression coincides with the earliest commitment to the macrophage lineage, Csf1r-EGFP bone marrow provides a tool for studying the earliest events in myelopoiesis using the sheep as a model.

Indexed as

AnimalsAnimals, Genetically ModifiedBiomarkersCell DifferentiationGreen Fluorescent ProteinsHumansLipopolysaccharide ReceptorsMacrophagesMiceMonocytesMyelopoiesisPromoter Regions, GeneticReceptors, Granulocyte-Macrophage Colony-Stimulating FactorReceptors, IgGSheepTransgenesBiomarkersCsf1r protein, mouseenhanced green fluorescent proteinGreen Fluorescent ProteinsLipopolysaccharide ReceptorsReceptors, Granulocyte-Macrophage Colony-Stimulating FactorReceptors, IgG

Identifiers

PMID27521343
PMCPMC5009875
OpenAlexW2512523106

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.