Evidence map›Paper›PMID 42908013›Full record

ArticleStem cell research & therapy2026

Hydrogels modified with IL4 or SDF1 mimicking peptides serve as a supportive environment for human iPSC-derived myoblasts.

Zuzanna Michalska, Anna Ostaszewska, Maria Dzierżyńska, Iwona Grabowska, Małgorzata Zimowska, Martyna Fularczyk, Piotr Skorupiński, Wanda Płoska, Aleksandra Romańska, Alicja Pluta and 6 more

Abstract read
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Article in Stem cell research & therapy, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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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

16 authors.

Zuzanna Michalska *Department of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Anna Ostaszewska *Department of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Maria DzierżyńskaDepartment of Biomedical Chemistry, Faculty of Chemistry, University of Gdańsk, Gdańsk, Poland.
Iwona GrabowskaDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Małgorzata ZimowskaDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Martyna FularczykDepartment of Biomedical Chemistry, Faculty of Chemistry, University of Gdańsk, Gdańsk, Poland.
Piotr SkorupińskiDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Wanda PłoskaDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Aleksandra RomańskaDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Alicja PlutaDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Zbigniew BartoszewiczDepartment of Internal Diseases and Endocrinology, Medical University of Warsaw, Warsaw, Poland.
Katarzyna Jańczyk-IlachDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Sylwia Rodziewicz-MotowidłoDepartment of Biomedical Chemistry, Faculty of Chemistry, University of Gdańsk, Gdańsk, Poland.
Maria A CiemerychDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland.
Edyta BrzoskaDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland. e.brzoska-wojt@uw.edu.pl.
Karolina ArchackaDepartment of Cytology, Faculty of Biology, Institute of Developmental Biology and Biomedical Sciences, University of Warsaw, Warsaw, Poland. k.archacka@uw.edu.pl.

Funding

National Science Centre 2019/35/B/NZ5/01555
6 · The paper itself

Abstract

backgroundSkeletal muscles are characterised by substantial regenerative potential, which may be insufficient in case of, e.g., extensive muscle damage, changes accompanying muscle diseases or ageing. For this reason, different ideas are being tested to develop efficient and safe approaches to treat such muscles. Among them, strategies based on biomaterials and stem cells or their derivatives play an important role.

methodsIn the current study, we tested RADA16-I-based hydrogels, modified with custom-designed IL4 or SDF1 mimicking peptides, as a tool that allows development, maintenance or even an increase of myogenic differentiation potential of human myoblasts derived from induced pluripotent stem cells (iPSCs), which are considered a source of cells in therapies for skeletal muscles. Since the release of abovementioned peptides from hydrogels requires activity of metalloproteinases (MMPs) we first assessed the expression of MMPs in iPSC-derived myoblasts cultured on hydrogels. Then we determined the influence of hydrogels on proliferation, apoptosis, and differentiation of iPSC-derived myoblasts as well as their transcriptome and secretome.

resultsWe found that the hydrogels designed by us allowed proper proliferation, migration, and myogenic differentiation of hiPSC-derived myoblasts. The latter was even increased in case of hydrogels functionalised with either IL4 or SDF1 peptides. Importantly, none of the hydrogels tested induced neither apoptosis nor unwanted differentiation, i.e. adipogenic, chondrogenic or osteogenic, of hiPSC-derived myoblasts. In response to hydrogel presence, changes in the expression of factors, such as CXCL8, FREM2, ADAMTS16, CDH9, IRS4, FIBIN, or MLIP involved in angiogenesis, inflammatory mediation, cell adhesion, neurogenesis, and regulation of myogenic program were observed.

conclusionsObtained results indicate that hydrogels functionalised with IL4 or SDF1 peptides serve as a supportive environment for myoblasts derived from hiPSCs and increase features that are beneficial for myogenic/regenerative potential of these cells.

Indexed as

Chemokine CXCL12HydrogelsInduced Pluripotent Stem CellsInterleukin-4MyoblastsPeptidesCell DifferentiationCell ProliferationHumansMuscle DevelopmentChemokine CXCL12CXCL12 protein, humanHydrogelsIL4 protein, humanInterleukin-4PeptidesHydrogelIL4 peptideiPSCsMyoblastsSDF1 peptideSkeletal muscle

Identifiers

PMID42908013
PMCPMC13689189

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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.