Evidence map›Paper›PMID 41959029›Full record

ArticlebioRxiv : the preprint server for biology2026

Deep Invaginations of Nuclear Envelope Coordinate Spatial Organization of Chromatin in Epithelium.

Elina Mäntylä, Sanna Korpela, Anna Rekonen, Sini Hakkola, Jenni Karttunen, Anni Pörsti, Sanni Erämies, Fábio Tadeu Arrojo Martins, Roselia Davidsson, Markus J T Ojanen and 10 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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

20 authors.

Elina MäntyläBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0000-0002-8681-8772
Sanna KorpelaBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0000-0003-1502-4630
Anna RekonenBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Sini HakkolaBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0009-0002-5282-5680
Jenni KarttunenBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0000-0002-0099-1305
Anni PörstiBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Sanni ErämiesBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0009-0002-8685-8130
Fábio Tadeu Arrojo MartinsBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0000-0002-3489-4095
Roselia DavidssonBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0009-0003-1828-6166
Markus J T OjanenBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0000-0001-6623-844X
Satu A-M HakanenNanoscience Center and Department of Biological and Environmental Science, University of Jyväskylä, Jyväskylä, Finland.
Peipei WangDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH, USA.ORCID 0000-0003-1431-2139
Joonas Uusi-MäkeläBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0009-0000-1755-4390
Alice Anais VarletWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY, USA.ORCID 0000-0002-1670-4884
Maija Vihinen-RantaNanoscience Center and Department of Biological and Environmental Science, University of Jyväskylä, Jyväskylä, Finland.ORCID 0000-0003-0959-1153
Daniel E ConwayDepartment of Biomedical Engineering, The Ohio State University, Columbus, OH, USA.ORCID 0000-0001-6624-177X
Keijo ViiriFaculty of Biochemistry and Molecular Medicine, University of Oulu, Oulu, Finland.ORCID 0000-0002-7167-5094
Matti NykterBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0000-0001-6956-2843
Jan LammerdingWeill Institute for Cell and Molecular Biology, Cornell University, Ithaca, NY, USA.ORCID 0000-0003-4335-8611
Teemu O IhalainenBioMediTech, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.ORCID 0000-0003-4351-8697

Funding

Cell junction and nuclear forces as mediators of epithelial cell homeostasisR35GM119617 · NIGMS · VIRGINIA COMMONWEALTH UNIVERSITY · PI Daniel E Conway · 2016 to 2026
$4.5M
Nuclear mechanobiology in confined migration (Equipment Supplement 2023)R01GM137605 · NIGMS · CORNELL UNIVERSITY · PI LAMMERDING, JAN · 2020 to 2023
$1.6M
Nuclear mechanobiology in confined migration (equipment supplement 2026)R35GM153257 · NIGMS · CORNELL UNIVERSITY · PI Jan Lammerding · 2024 to 2026
$1.3M
NIGMS NIH HHS R01 GM137605NIGMS NIH HHS R35 GM119617NIGMS NIH HHS R35 GM153257
6 · The paper itself

Abstract

Cell nuclei are often used to assess cell health, but how their shapes vary in normal tissues and how they respond to mechanical forces is not well understood. Here, we describe deep invaginations of the nuclear envelope (DINEs) as common features of epithelial cell nuclei. After their formation, DINEs exist independently of the cytoskeleton, depend on A-type lamins, and emerge in response to cell crowding, contact inhibition, and tissue maturation. High-resolution imaging shows that, in contrast to the peripheral nuclear lamina, DINEs contain densely packed chromatin with regions of active gene transcription. They also remodel dynamically during confined migration, allowing nuclei to adapt to physical constraints. Mechanistically, DINE formation is linked to suppression of MAPK signaling, while activation of growth-promoting pathways reduces their occurrence. These findings reveal DINEs as intrinsic, mechanosensitive structures that coordinate nuclear shape, chromatin organization, and gene activity, providing new insight into how epithelial cells integrate mechanical and biochemical cues to maintain tissue homeostasis.

Identifiers

PMID41959029
PMCPMC13061027

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Registered trials

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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.