Evidence map›Paper›PMID 41181706›Full record

ArticleFrontiers in cell and developmental biology2025

Aspects of zone-like identity and holotomographic tracking of human stem cell-derived liver sinusoidal endothelial cells.

Mikel Amirola-Martinez, Thomas Combriat, Katharina Ferencevic, Ingrid Wilhelmsen, Andrea Dalmao-Fernandez, Petter Angell Olsen, Justyna Stokowiec, Aleksandra Aizenshtadt, Stefan Krauss

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 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
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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

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

9 authors.

Mikel Amirola-MartinezHybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.
Thomas CombriatHybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.
Katharina FerencevicHybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.
Ingrid WilhelmsenHybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.
Andrea Dalmao-FernandezHybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.
Petter Angell OlsenHybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.
Justyna StokowiecHybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.
Aleksandra Aizenshtadt *Hybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.
Stefan Krauss *Hybrid Technology Hub, Institute of Basic Medical Research, University of Oslo, Oslo, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Liver sinusoidal endothelial cells (LSEC) are specialized endothelial cells with unique metabolic and barrier functions adapted to the needs of the liver sinusoid. LSECs are highly sensitive to their environment, and this fragile nature causes challenges in analyzing their phenotype under Methods: In this work, we first differentiated LSEC-like cells (scLSECs) from two human pluripotent stem cell lines and characterized them by a panel of qPCR markers, immunohistochemistry, substrate oxidation for energy metabolism, scavenger function, and nitric oxide secretion. We then introduced holotomography, a technique that allows to recover quantitative and three-dimensional information about the refractive indexes of cell components, as a tool to image and track scLSEC Results and discussion: Holotomography and developed machine learning-based algorithm for image processing allowed us to describe and monitor changes in intracellular pore-like structures over time. Finally, we tested the possibility of inducing aspects of zone-specific LSEC phenotype and metabolism using culture-based treatments, which resulted in modest shifts in marker expression and metabolic activity. The presented strategy provides an advanced tool kit for investigating liver endothelial cells.

Indexed as

fenestrationholotomography (HT)liver zonationLSECpluripotent stem cells (PSC)

Identifiers

PMID41181706
PMCPMC12575375

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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.