Evidence map›Paper›PMID 41093855›Full record

ArticleNature communications2025

In vivo mechano-tissue engineering by hydrogels capable of transmitting intercellular mechanical stress.

Natsumi Ueda, Hayato Okazaki, Akihiro Mikuma, Ayane Kunieda, Soma Kawashima, Takeru Torii, Keiko Kawauchi, Masatake Matsuoka, Tomohiro Onodera, Norimasa Iwasaki and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. 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. Review
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

11 authors.

Natsumi UedaDepartment of Nanobiochemistry, Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Hyogo, Japan.
Hayato OkazakiDepartment of Nanobiochemistry, Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Hyogo, Japan.
Akihiro MikumaDepartment of Nanobiochemistry, Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Hyogo, Japan.
Ayane KuniedaDepartment of Nanobiochemistry, Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Hyogo, Japan.
Soma KawashimaDepartment of Nanobiochemistry, Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Hyogo, Japan.
Takeru ToriiDepartment of Nanobiochemistry, Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Hyogo, Japan.ORCID http://orcid.org/0000-0002-6278-7617
Keiko KawauchiDepartment of Nanobiochemistry, Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Hyogo, Japan.ORCID http://orcid.org/0000-0002-8276-7277
Masatake MatsuokaDepartment of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Tomohiro OnoderaDepartment of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Norimasa IwasakiDepartment of Orthopaedic Surgery, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Koji NagahamaDepartment of Nanobiochemistry, Frontiers of Innovative Research in Science and Technology (FIRST), Konan University, Hyogo, Japan. nagahama@konan-u.ac.jp.ORCID http://orcid.org/0000-0002-4718-7971

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) KAKENHI 23K2521
6 · The paper itself

Abstract

Integrating the latest insights from mechanobiology into tissue engineering could lead to innovative technologies. Here we show a method to effectively elicit the regenerative response of transplanted cells by utilizing mechanical stress generated in vivo. The essential feature of our method is that it does not use specific ligands for the vital mechanosensor integrins to mechanically activate them. In our method, azide groups are introduced into the integrin, and the hydrogel is modified with cyclooctyne (DBCO) groups. Thus, bioorthogonal click reaction between the azide groups and the DBCO groups forms direct, stable, irreversible covalent bonds between the cellular integrin and the hydrogel. We demonstrate that the integrin-hydrogel linkage is in ON state regardless of the intensity of the stress, the cell cycle, or the extracellular environment, so that mechanical stress is rapidly and reliably transmitted to the nucleus through the linkage in vivo, resulting in regenerative response of the transplanted cells.

Indexed as

HydrogelsMechanotransduction, CellularStress, MechanicalTissue EngineeringAnimalsAzidesClick ChemistryCyclooctanesHumansIntegrinsMiceRegenerationAzidesCyclooctanesHydrogelsIntegrins

Identifiers

PMID41093855
PMCPMC12528752

What OpenQuestion holds

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LicenceCC BY-NC-ND
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 OpenQuestion graph.