Evidence map›Paper›PMID 41326596›Full record

ArticleScientific reports2025

Proteomic and morphologic characterization of ovine macrophage differentiation and polarization.

A Elkhamary, C Gerner, A Bileck, I Gerner, F Jenner

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

A ElkhamaryDepartment for Companion Animals and Horses, Centre for Equine Health and Research, Veterm, Vetmeduni Vienna, Vienna, Austria.
C GernerDepartment of Analytical Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
A BileckDepartment of Analytical Chemistry, Faculty of Chemistry, University of Vienna, Vienna, Austria.
I GernerDepartment for Companion Animals and Horses, Centre for Equine Health and Research, Veterm, Vetmeduni Vienna, Vienna, Austria.
F JennerDepartment for Companion Animals and Horses, Centre for Equine Health and Research, Veterm, Vetmeduni Vienna, Vienna, Austria. florien.jenner@vetmeduni.ac.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages play crucial roles in inflammation and tissue homeostasis, exhibiting phenotypic and functional plasticity that enables them to initiate, sustain, or resolve inflammation. To support the evidence-based selection of biomedically relevant preclinical models, this study comprehensively characterized ovine macrophage differentiation and polarization by integrating morphological assessments with in-depth proteomic profiling of cellular lysates and secretomes. Monocytes isolated from peripheral blood were differentiated into macrophages using GM-CSF (GMØ) or M-CSF (MMØ), then polarized into M1 and M2 phenotypes. Mass spectrometry identified 4804 proteins in cell lysates and 901 in secretomes, including 42 CD antigens, enabling the establishment of CD marker profiles for monocytes and the distinct macrophage differentiation and polarization states. Proteomic analyses revealed significant upregulation of inflammatory markers in M1 and elevated tissue repair markers in M2 macrophages. Enrichment analysis confirmed activation of antimicrobial and matrix-degrading pathways in M1 macrophages, and regenerative, proteolysis-inhibiting functions in M2 macrophages. In conclusion, this study addresses the limitations of currently available immunological tools by providing an antibody-independent alternative for the classification of ovine macrophages, facilitating more precise phenotypic characterization and functional insight in ovine immunology research.

Indexed as

Cell DifferentiationMacrophagesProteomeProteomicsAnimalsGranulocyte-Macrophage Colony-Stimulating FactorMonocytesSheepGranulocyte-Macrophage Colony-Stimulating FactorProteome

Identifiers

PMID41326596
PMCPMC12780204

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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.