Evidence map›Paper›PMID 37639117›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Genetic and Immunohistochemistry Tools to Visualize Rat Macrophages In Situ.

Stephen Huang, Dylan Carter-Cusack, Emma Maxwell, Omkar L Patkar, Katharine M Irvine, David A Hume

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
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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.

Stephen HuangMater Research Institute-UQ, Translational Research Institute, Woolloongabba, Brisbane, QLD, Australia.
Dylan Carter-CusackMater Research Institute-UQ, Translational Research Institute, Woolloongabba, Brisbane, QLD, Australia.
Emma MaxwellMater Research Institute-UQ, Translational Research Institute, Woolloongabba, Brisbane, QLD, Australia.
Omkar L PatkarMater Research Institute-UQ, Translational Research Institute, Woolloongabba, Brisbane, QLD, Australia.
Katharine M IrvineMater Research Institute-UQ, Translational Research Institute, Woolloongabba, Brisbane, QLD, Australia. Katharine.Irvine@mater.uq.edu.au.
David A HumeMater Research Institute-UQ, Translational Research Institute, Woolloongabba, Brisbane, QLD, Australia. David.hume@uq.edu.au.
Translational Research Institute · AUMater Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages contribute to many aspects of development and homeostasis, innate and acquired immunity, immunopathology, and tissue repair. Every tissue contains an abundant resident macrophage population. Inflammatory stimuli promote the recruitment of monocytes from the blood and their adaptation promotes the removal of the stimulus and subsequent restoration of normal tissue architecture. Dysregulation of this response leads to chronic inflammation and tissue injury. In many tissues, their differentiation and survival are dependent on the colony stimulating factor 1 receptor (CSF1R) signalling axis, which is highly conserved across all vertebrates. Complete loss of either CSF1R or its cognate ligands, colony stimulating factor 1 (CSF1), and interleukin 34 (IL-34), results in the loss of many tissue-resident macrophage populations. This provides a useful paradigm to study macrophages.There are many tools used to visualize tissue-resident macrophages and their precursors, monocytes, in mice and humans. Particularly in mice there are genetic tools available to delete, enhance and manipulate monocytes and macrophages and their gene products to gain insight into phenotype and function. The laboratory rat has many advantages as an experimental model for the understanding of human disease, but the analytical resources are currently more limited than in mice. Here, we describe available genetic models, antibodies, and immunohistochemistry (IHC) methods that may be used to visualize tissue-resident macrophages in rats.

Indexed as

Macrophage Colony-Stimulating FactorMacrophagesAcclimatizationAnimalsHumansImmunohistochemistryMiceMonocytesRatsReceptor Protein-Tyrosine KinasesMacrophage Colony-Stimulating FactorReceptor Protein-Tyrosine KinasesCRISPRCSF1CSF1RIBA1IL-34MPSReporter rat

Identifiers

PMID37639117
OpenAlexW4386209507

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.