Evidence map›Paper›PMID 41696151›Full record

ArticleMaterials today. Bio2026

Piezo1 regulates remodeling of skin-derived extracellular matrix by embedded umbilical cord mesenchymal stem cells in a stiffness-dependent fashion.

Fenghua Zhao, Xue Zhang, Theo Borghuis, Linda A Brouwer, Janette K Burgess, Prashant K Sharma, Martin C Harmsen

Abstract read
In one paragraph

Article in Materials today. Bio, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Fenghua ZhaoUniversity of Groningen, University Medical Centre Groningen, Department of Biomaterials and Biomedical Technology-FB40, A. Deusinglaan 1, Groningen, 9713 AV, the Netherlands.
Xue ZhangUniversity of Groningen, University Medical Centre Groningen, Department of Pathology and Medical Biology, Hanzeplein 1 (EA11), Groningen, 9713 GZ, the Netherlands.
Theo BorghuisUniversity of Groningen, University Medical Centre Groningen, Department of Pathology and Medical Biology, Hanzeplein 1 (EA11), Groningen, 9713 GZ, the Netherlands.
Linda A BrouwerUniversity of Groningen, University Medical Centre Groningen, Department of Pathology and Medical Biology, Hanzeplein 1 (EA11), Groningen, 9713 GZ, the Netherlands.
Janette K BurgessUniversity of Groningen, University Medical Centre Groningen, Department of Pathology and Medical Biology, Hanzeplein 1 (EA11), Groningen, 9713 GZ, the Netherlands.
Prashant K SharmaUniversity of Groningen, University Medical Centre Groningen, Department of Biomaterials and Biomedical Technology-FB40, A. Deusinglaan 1, Groningen, 9713 AV, the Netherlands.
Martin C HarmsenUniversity of Groningen, University Medical Centre Groningen, Department of Pathology and Medical Biology, Hanzeplein 1 (EA11), Groningen, 9713 GZ, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cells continuously sense and adapt to the mechanical properties of their surrounding extracellular matrix (ECM), yet how human umbilical cord-derived mesenchymal stromal cells (UC-MSCs) mechanotransduce stiffness cues in 3D ECM remains incompletely understood. This knowledge gap limits the rational design of MSC-based regenerative therapies and mechanically instructive biomaterials. Here, using ruthenium-catalyzed photocrosslinked skin-derived ECM hydrogels spanning a physiological to fibrotic stiffness range, we demonstrate that UC-MSCs exhibit distinct, stiffness-dependent remodeling strategies. Soft matrices (1.2 kPa) induced cell-mediated hydrogel contraction, medium stiffness (3.4 kPa, comparable to native skin) supported elongated cell morphology with minimal remodeling, whereas stiff matrices (17.7 kPa) kept seeded UC-MSCs rounded and induced pericellular void formation consistent with localized ECM remodeling. By decoupling geometric contraction from intrinsic ECM turnover using volume-normalized mechanical analyses, we identify the Piezo1 as a key regulator of stiffness-dependent adaptation. Piezo1 expression increased with stiffness, and its inhibition attenuated contraction in soft matrices and prevented stiffness reduction in stiff matrices, indicating that Piezo1 enables MSCs to mechanically adapt across 3D microenvironments. Analysis of matrix metalloproteinase expression revealed stiffness-dependent regulation of MMP2 and MMP14; however, their expression was only marginally affected by Piezo1 inhibition, suggesting that Piezo1 influences ECM remodeling through mechanisms beyond direct regulation of MMP expression. Together, these findings establish a mechanistic framework in which UC-MSCs adapt to 3D ECM stiffness through Piezo1-dependent mechanosensing. This work provides conceptual and practical guidance for the design of mechanically programmable biomaterials, the optimization of MSC-based regenerative strategies, and therapeutic approaches aimed at modulating pathological tissue mechanics such as fibrosis.

Indexed as

ECM remodelingFibrotic environmentsMechanotransductionPiezo1StiffnessUC-MSCs

Identifiers

PMID41696151
PMCPMC12906116

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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.