Evidence map›Paper›PMID 41708751›Full record

ArticleScientific reports2026

Traction force transmission via bioactive matrix hydrogel promotes epithelial collective migration mediated by integrin.

Mingxing Ouyang, Yu Cao, Hui Sheng, Hongjie Liu, Lei Liu, Chunmei Li, Bing Bu, Linhong Deng

Abstract read
In one paragraph

Article in Scientific reports, 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

8 authors.

Mingxing Ouyang *Institute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering, Changzhou University, 1 Gehu Rd, Wujin District, Changzhou, 213164, Jiangsu Province, China. mxouyang@cczu.edu.cn.
Yu Cao *Institute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering, Changzhou University, 1 Gehu Rd, Wujin District, Changzhou, 213164, Jiangsu Province, China.
Hui ShengInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering, Changzhou University, 1 Gehu Rd, Wujin District, Changzhou, 213164, Jiangsu Province, China.
Hongjie LiuInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering, Changzhou University, 1 Gehu Rd, Wujin District, Changzhou, 213164, Jiangsu Province, China.
Lei LiuInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering, Changzhou University, 1 Gehu Rd, Wujin District, Changzhou, 213164, Jiangsu Province, China.
Chunmei LiInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering, Changzhou University, 1 Gehu Rd, Wujin District, Changzhou, 213164, Jiangsu Province, China.
Bing BuInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering, Changzhou University, 1 Gehu Rd, Wujin District, Changzhou, 213164, Jiangsu Province, China.
Linhong DengInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering, Changzhou University, 1 Gehu Rd, Wujin District, Changzhou, 213164, Jiangsu Province, China. dlh@cczu.edu.cn.

Funding

National Natural Science Foundation of China NSFC 12272063National Natural Science Foundation of China NSFC 12372312
6 · The paper itself

Abstract

Mechanical communications provide physical views to understand cell physiologies at large scale. Cell collective migration occurs often in vivo, of which the role of matrix tension force is largely unknown. Here to mimic in vivo conditions, we applied collective migration of renal epithelial MDCK cells on elastic matrix hydrogel containing bioactive materials of 50% Matrigel and 1 mg/mL type I collagen. MDCK cells were engineered with stable expression of ERK FRET (fluorescence energy resonance transfer) biosensor in regarding of ERK sensitivity in cell mechanical response. The results showed that matrix traction force derived from cells-generated contraction promoted epithelial sheet migration with higher ERK activity at the move front. Hydrogel crosslinking by glutaraldehyde blocked matrix traction transmission and then reduced ERK and epithelial collective migration. Integrin inhibition dramatically reduced collective migration but not local cell moving velocities, indicating integrin acting with mechanotransduction role at cells-hydrogel interface in orienting migration direction. Further experiments demonstrated that matrix traction force relied on activations of cellular mechanosensitive calcium channels, and ERK signal in promoting collective migration. In conclusion, matrix tension force derived from cell contractions facilitates epithelial collective migration through activating cellular mechanosensitive signals, in which integrin acts as mechanical transducer. This work highlights the role of matrix traction force in wound healing and tissue engineering.

Indexed as

Cell MovementEpithelial CellsExtracellular MatrixHydrogel, Polyethylene Glycol DimethacrylateHydrogelsIntegrinsMechanotransduction, CellularAnimalsCollagenDogsDrug CombinationsFluorescence Resonance Energy TransferLamininMadin Darby Canine Kidney CellsProteoglycansCollagenDrug CombinationsHydrogel, Polyethylene Glycol DimethacrylateHydrogelsIntegrinsLamininmatrigelProteoglycansCell mechanical communicationsEpithelial collective migrationERKFluorescence resonance energy transfer (FRET)IntegrinMatrix traction force

Identifiers

PMID41708751
PMCPMC12988202

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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.