Evidence map›Paper›PMID 42360388›Full record

ArticleCell and tissue research2026

Deletion of CEACAM1 does not affect retinal and choroidal morphology or transcriptome.

Laura Hannig, Barbara M Braunger, Nikolai Kleefeldt, Lea Cagol, Jonathan Zimmermann, Bianka Brunne, Hamza Ahmad, Mario Vallon, Süleyman Ergün, Jost Hillenkamp and 2 more

Abstract read
In one paragraph

Article in Cell and tissue research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

12 authors.

Laura HannigInstitute of Neuroanatomy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Barbara M BraungerInstitute of Neuroanatomy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Nikolai KleefeldtDepartment of Ophthalmology, Universitaetsklinikum Würzburg, Würzburg, Germany.
Lea CagolInstitute of Anatomy and Cell Biology, Julius-Maximilians-University Würzburg, Würzburg, Germany.
Jonathan ZimmermannInstitute of Anatomy and Cell Biology, Julius-Maximilians-University Würzburg, Würzburg, Germany.
Bianka BrunneInstitute of Neuroanatomy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Hamza AhmadInstitute of Neuroanatomy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Mario VallonInstitute of Anatomy and Cell Biology, Julius-Maximilians-University Würzburg, Würzburg, Germany.
Süleyman ErgünInstitute of Anatomy and Cell Biology, Julius-Maximilians-University Würzburg, Würzburg, Germany.
Jost HillenkampDepartment of Ophthalmology, Universitaetsklinikum Würzburg, Würzburg, Germany.
Andreas NeuederInstitute for Molecular Neurogenetics, Center for Molecular Neurobiology Hamburg, University Clinic Hamburg-Eppendorf, Hamburg, Germany.
Anja SchlechtInstitute of Neuroanatomy, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. a.schlecht@uke.de.ORCID https://orcid.org/0000-0003-3336-9982

Funding

Helmut Ecker Stiftung 01/23
6 · The paper itself

Abstract

CEACAM1 (CC1) is an important mediator of cell proliferation and adhesion and serves as an angiogenic factor through interaction with VEGF. Although the role of CC1 has been extensively studied in organs such as the heart, liver and lung in which CC1 is considered an important regulator of various pathological conditions, little is known about the function of CEACAM1 in the eye. In this study, we investigated the expression and function of CC1 in the retina and choroid of healthy adult mice using immunohistochemistry, fluorescence activated cell sorting (FACS) and RNA sequencing. We found CC1 to be expressed in endothelial and myeloid cells of the retina and the choroid. However, deletion of CC1 did not result in vascular abnormalities of the retina and choroid or changes in retinal myeloid cell morphology and number. Furthermore, the retinal architecture was not affected and morphometric measurements of the thickness of the inner and outer retinal layers were not altered by deletion of CC1. Accordingly, we did not observe structural or transcriptomic changes in the choroid. Our data suggest that the role of CC1 in the adult eye during steady state is attenuated or can be compensated by other molecular mediators. However, one could speculate that CC1 may become functionally relevant during pathological conditions, such as in neovascular eye diseases like proliferative diabetic retinopathy or neovascular age-related macular degeneration.

Indexed as

CEACAM1 ProteinChoroidGene DeletionRetinaTranscriptomeAnimalsCarcinoembryonic AntigenMiceMice, Inbred C57BLMice, KnockoutCarcinoembryonic AntigenCEACAM1 ProteinCeacam1 protein, mouseCC1CEACAM1ChoroidHomeostasisRetina

Identifiers

PMID42360388
PMCPMC13309465

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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.