Evidence map›Paper›PMID 41954370›Full record

ArticleAnnals of the New York Academy of Sciences2026

Detection of Mesenchymal Stem Cell Aging Using an Integrin Mechano-Probe.

Aimei Liu, Xiaojun Liu, Juan Li, Jiangtao Li, Xinpeng Wang, Yuanjun Dong, Feng Shao, Mingjun Bi, Xiaoyan Deng, Guixue Wang and 1 more

Abstract read
In one paragraph

Article in Annals of the New York Academy of Sciences, 2026. 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
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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

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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

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.

Aimei LiuSchool of Life Sciences and Health, University of Health and Rehabilitation Sciences, Qingdao, Shandong, PR China.
Xiaojun LiuSchool of Life Sciences and Health, University of Health and Rehabilitation Sciences, Qingdao, Shandong, PR China.
Juan LiDepartment of Quality Management, Qingdao Special Servicemen Recuperation Center of PLA NAVY, Qingdao, PR China.
Jiangtao LiSchool of Life Sciences and Health, University of Health and Rehabilitation Sciences, Qingdao, Shandong, PR China.
Xinpeng WangSchool of Rehabilitation Science and Engineering, University of Health and Rehabilitation Sciences, Qingdao, Shandong, PR China.
Yuanjun DongSchool of Social Development, University of Health and Rehabilitation Sciences, Qingdao, Shandong, PR China.
Feng ShaoKey Laboratory of Marine Chemistry Theory and Technology, Ministry of Education, College of Chemistry and Chemical Engineering, Ocean University of China, Qingdao, PR China.
Mingjun BiAdvanced Medical Research Institute, Cheeloo, College of Medicine, Shandong University, Jinan, PR China.
Xiaoyan DengKey Laboratory of Biomechanics and Mechanobiology of Ministry of Education, Beijing Advanced Innovation Center For Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing, PR China.
Guixue WangKey Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory For Vascular Implants, Bioengineering College of Chongqing University, Chongqing, PR China.
Yongliang WangSchool of Life Sciences and Health, University of Health and Rehabilitation Sciences, Qingdao, Shandong, PR China.

Funding

National Natural Science Foundation of China 12032007National Natural Science Foundation of China 31971242National Natural Science Foundation of China 82200597National Natural Science Foundation of China 82401622Natural Science Foundation of Shandong Province ZR2023QC286Natural Science Foundation of Shandong Province ZR2023QH131Shandong Natural Science Foundation for Excellent Young Scholars (Overseas) 2023HWYQ-084Taishan Scholar Project of Shandong Province tsqn202306360
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) play a crucial role in cell therapy, but their efficacy diminishes with age. While biochemical methods like flow cytometry, immunoblotting, β-galactosidase labeling, and gene profiling are effective for screening MSC aging, mechanical factors also change with aging. After analyzing the transcriptomes of young and aged MSCs, we observed downregulation of adhesion-related genes and, based on those data, developed an integrin mechano-probe to measure integrin forces in MSCs. The probe's effectiveness was validated by mapping integrin forces in young and aged MSCs, revealing reduced integrin force signals in aged cells that correlated with downregulated expression of β1 integrins. This finding was further confirmed by flow cytometry and β-galactosidase staining. Overexpression of integrin β1 in aged MSCs restored mechanical signaling and increased p-ERK production, suggesting that the integrin β1/ERK pathway plays a role in rescuing the contractility of aged MSCs. Our mechano-probe enables distinguishing aged MSCs in a mixed pool of young and aged MSCs and identifying aged MSCs taken from mouse tissue. Integrin tension signals, as measured by a mechano-probe, may thus complement biochemical markers in assessing MSC aging.

Indexed as

Cellular SenescenceIntegrin beta1IntegrinsMesenchymal Stem CellsAnimalsHumansMechanotransduction, CellularMiceIntegrin beta1IntegrinsagingGFP probeintegrin tensionmesenchymal stem cell

Identifiers

PMID41954370
PMCPMC13064422

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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.