Evidence map›Paper›PMID 41213920›Full record

ArticleCell death discovery2025

Effects of Notch signaling on the lineage commitment of human peripheral blood monocyte trilineage progenitor under inflammatory conditions.

Sara Aničić, Maša Filipović, Ivo Krešić, Ozana Jakšić, Marta Radošević, Darja Flegar, Pavao Planinić, Marina Ikić Matijašević, Zrinka Jajić, Tomislav Kelava and 3 more

Abstract read
In one paragraph

Article in Cell death discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Sara AničićLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.
Maša FilipovićLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.ORCID http://orcid.org/0000-0003-2793-8675
Ivo KrešićDepartment of Physiology, School of Medicine, University of Mostar, Mostar, Bosnia and Herzegovina.
Ozana JakšićLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.
Marta RadoševićLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.ORCID http://orcid.org/0009-0000-7828-1920
Darja FlegarLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.ORCID http://orcid.org/0000-0002-3181-5849
Pavao PlaninićDepartment of Physiology, School of Medicine, University of Mostar, Mostar, Bosnia and Herzegovina.
Marina Ikić MatijaševićDepartment of Clinical Immunology, Rheumatology, and Pulmonology, University Hospital "Sveti Duh", Zagreb, Croatia.
Zrinka JajićDepartment of Rheumatology, Physical Medicine, and Rehabilitation, Clinical Hospital Center "Sestre Milosrdnice", University of Zagreb School of Medicine, Zagreb, Croatia.
Tomislav KelavaLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.ORCID http://orcid.org/0000-0002-6665-116X
Nataša KovačićLaboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia.ORCID http://orcid.org/0000-0001-6042-2107
Alan Šućur *Laboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia. alan.sucur@mef.hr.ORCID http://orcid.org/0000-0001-7523-1047
Danka Grčević *Laboratory for Molecular Immunology, Croatian Institute for Brain Research, University of Zagreb School of Medicine, Zagreb, Croatia. danka.grcevic@mef.hr.ORCID http://orcid.org/0000-0002-2365-8249

Funding

Hrvatska Zaklada za Znanost (Croatian Science Foundation) HRZZ-DOK-2021-02-6365Hrvatska Zaklada za Znanost (Croatian Science Foundation) HRZZ-DOK-NPOO-2023-10-4220Hrvatska Zaklada za Znanost (Croatian Science Foundation) HRZZ-IP-2022-10-2285
6 · The paper itself

Abstract

Rheumatoid arthritis (RA) is a chronic autoimmune inflammatory disease, causing significant morbidity and disability. Inflammation-induced activation of myeloid cells is involved in disease pathogenesis and contributes to joint destruction. Due to the significant plasticity of myeloid lineage, peripheral blood (PBL) monocytes have the potential to differentiate into a variety of mature cells, including macrophages, osteoclasts, and dendritic cells (DCs), depending on the environmental cues and activated signaling pathways. Therefore, we aimed to determine how the Notch pathway affects differentiation of human PBL monocyte progenitor under inflammatory conditions. We first determined the frequency of monocyte subsets and identified a common trilineage monocyte progenitor (TMP), expressing the phenotype CD45

Identifiers

PMID41213920
PMCPMC12602708

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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.