Evidence map›Paper›PMID 41674897›Full record

ArticleJHEP reports : innovation in hepatology2026

3D endothelial cell scaffolds protect liver explants and exhibit therapeutic effects on liver fibrosis.

Mireia Medrano-Bosch, Alazne Moreno-Lanceta, Blanca Simón-Codina, David Saavedra-Pérez, Yiliam Fundora, Francisco J Sánchez, Meritxell Perramón, Laura Macias-Muñoz, Manuel Morales-Ruiz, Elazer R Edelman and 2 more

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 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

12 authors.

Mireia Medrano-BoschDepartment of Biomedicine, School of Medicine, University of Barcelona, Barcelona, Spain.
Alazne Moreno-LancetaDepartment of Biomedicine, School of Medicine, University of Barcelona, Barcelona, Spain.
Blanca Simón-CodinaDepartment of Biomedicine, School of Medicine, University of Barcelona, Barcelona, Spain.
David Saavedra-PérezLiver Transplant Unit, Institut Clínic de Malalties Digestives i Metabòliques (ICMDM), Hospital Clínic, University of Barcelona, Barcelona, Spain.
Yiliam FundoraInstitut d'Investigacions Biomèdiques August Pi-Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Barcelona, Spain.
Francisco J SánchezLiver Transplant Unit, Institut Clínic de Malalties Digestives i Metabòliques (ICMDM), Hospital Clínic, University of Barcelona, Barcelona, Spain.
Meritxell PerramónInstitut d'Investigacions Biomèdiques August Pi-Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Barcelona, Spain.
Laura Macias-MuñozInstitut d'Investigacions Biomèdiques August Pi-Sunyer (IDIBAPS), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Barcelona, Spain.
Manuel Morales-RuizDepartment of Biomedicine, School of Medicine, University of Barcelona, Barcelona, Spain.
Elazer R EdelmanInstitute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA, USA.
Wladimiro JiménezDepartment of Biomedicine, School of Medicine, University of Barcelona, Barcelona, Spain.
Pedro Melgar-LesmesDepartment of Biomedicine, School of Medicine, University of Barcelona, Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: Endothelial cells (ECs) display myriad protective roles that support tissue homeostasis. Embedding healthy ECs in 3D scaffolds stabilizes their phenotype to maximize reparative effects and shields immunogenicity. Here, we evaluate the protective effects of matrix-embedded ECs (MEECs) in liver explants and models of chronic liver disease. Methods: Precision cut liver slices (PCLS) from patients with cirrhosis (n = 8) and fibrotic or healthy mice (n = 6) were co-cultured with MEECs for 24 h and hepatic viability and inflammation were analyzed. The protective effects of the MEECs secretome were explored Results: MEECs protected liver viability in PCLS from patients with cirrhosis (ATP/protein, 2.7 Conclusions: Endothelial-hepatocyte regulation is essential in liver repair, and matrix-embedded endothelial cells (MEECs) appear to be a potential therapy for chronic liver injury and Impact and implications: Organ transplantation is the most effective therapy for advanced liver disease, yet remains limited by preservation of harvested graft viability and injury-induced inflammation post implantation. Healthy ECs display myriad protective roles that contribute to tissue homeostasis. In this study, we show how MEECs preserve cell viability and reduce inflammation in hepatic explants and display anti-inflammatory, antifibrotic and pro-regenerative properties in the liver of fibrotic mice. These dynamic and unique hepatoprotective properties of MEECs highlight their potential therapeutic utility for chronic liver injury or

Indexed as

Cell therapyEndothelial cellsFibrosisInflammationLiverRegeneration

Identifiers

PMID41674897
PMCPMC12890448

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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.