Evidence map›Paper›PMID 40640572›Full record

ArticleCommunications biology2025

Sweet and sticky: increased cell adhesion through click-mediated functionalization of regenerative liver progenitor cells.

Amaziah R Alipio, Melissa R Vieira, Tamara Haefeli, Lisa Hoelting, Olivier Frey, Alicia J El Haj, Maria C Arno

Abstract read
In one paragraph

Article in Communications 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
–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

7 authors.

Amaziah R AlipioSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham, UK.ORCID http://orcid.org/0009-0000-7101-5515
Melissa R VieiraHealthcare Technologies Institute, Institute of Translational Medicine, University of Birmingham, Edgbaston, Birmingham, UK.ORCID http://orcid.org/0009-0002-7956-0213
Tamara HaefeliInSphero AG, Wagistrasse 27A, Schlieren, Switzerland.
Lisa HoeltingInSphero AG, Wagistrasse 27A, Schlieren, Switzerland.
Olivier FreyInSphero AG, Wagistrasse 27A, Schlieren, Switzerland.
Alicia J El HajHealthcare Technologies Institute, Institute of Translational Medicine, University of Birmingham, Edgbaston, Birmingham, UK. a.elhaj@bham.ac.uk.ORCID http://orcid.org/0000-0003-3544-5678
Maria C ArnoSchool of Chemistry, University of Birmingham, Edgbaston, Birmingham, UK. m.c.arno@bham.ac.uk.ORCID http://orcid.org/0000-0003-1734-4777

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 789119RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/ SO2347X/1RCUK | Engineering and Physical Sciences Research Council (EPSRC) EP/X037622/1RCUK | Medical Research Council (MRC) 623924RCUK | Medical Research Council (MRC) 996932RCUK | Medical Research Council (MRC) MR/X033546/1
6 · The paper itself

Abstract

The burgeoning field of cell therapies is rapidly expanding, offering the promise to tackle complex and unsolved healthcare problems. One prominent example is represented by CAR T-cells, which have been introduced into the clinic for treating a variety of cancers. Promising cell therapeutics have also been developed to promote tissue regeneration, showing high potencies for the treatment of damaged liver. Nevertheless, in the remit of regenerative medicine, cell-therapy efficacies remain suboptimal as a consequence of the low engraftment of injected cells to the existing surrounding tissue. Herein, we present a facile approach to enhance the adhesion and engraftment of therapeutic hepatic progenitor cells (HPCs) through specific and homogeneous cell surface modification with exogenous polysaccharides, without requiring genetic modification. Coated HPCs exhibit significantly increased markers of adhesion and cell spreading and demonstrate preferential interactions with certain extra-cellular matrix proteins. Moreover, they display enhanced binding to endothelial cells and 3D liver microtissues. This translatable methodology shows promise for improving therapeutic cell engraftment, offering a potential alternative to liver transplantation in end-stage liver disease.

Indexed as

Cell AdhesionLiverLiver RegenerationStem CellsStem Cell TransplantationAnimalsClick ChemistryHepatocytesHumansMice

Identifiers

PMID40640572
PMCPMC12246442

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.