Evidence map›Paper›PMID 40745673›Full record

ArticleJournal of cellular and molecular medicine2025

The Mechanosensitive Ion Channel Piezo1 Regulates Chondrocyte Homeostasis Through the PI3K/AKT/mTORC1 Pathway in Osteoarthritis.

Yuanyuan Han, Fangyan Cheng, Xinyan Li, Jiahao Yu, Guimiao Li, Wei Chen, Jiaxue Zhang, Chen Feng, Yingze Zhang, Juan Wang

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
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  5. [Research progress on clinical transformation of Piezo1 in osteoarthritis].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2026
    Review
  6. Review
  7. Review
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  10. 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

10 authors.

Yuanyuan HanOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.ORCID 0009-0000-9510-9583
Fangyan ChengOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.
Xinyan LiOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.
Jiahao YuOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.
Guimiao LiOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.
Wei ChenNHC Key Laboratory of Intelligent Orthopaedic Equipment, Hebei Medical University Third Hospital, Shijiazhuang, China.
Jiaxue ZhangOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.
Chen FengOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.
Yingze ZhangOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.
Juan WangOrthopaedic Research Institution of Hebei Province, Shijiazhuang, China.ORCID 0009-0000-1801-0045

Funding

Medical Science Research Project of Hebei 20210692National Natural Science Foundation of China 82002368National Natural Science Foundation of China 82172466National Natural Science Foundation of China 91949203National Natural Science Foundation of China U23A6008Natural Science Foundation of Hebei Province H2020206377
6 · The paper itself

Abstract

Osteoarthritis (OA) is a highly prevalent chronic joint disease with complicated pathogenesis, causing pain and dysfunction. The mechanosensitive ion channel Piezo1 is an important mechanoreceptor on chondrocytes and may be involved in the process of OA. However, its role and mechanism remain elusive. This study investigated the role and possible mechanisms of Piezo1 in OA induced by excessive mechanical stress. Piezo1 expression levels were markedly up-regulated in the lesioned region of the medial tibial cartilage in OA rats subjected to destabilisation of the medial meniscus (DMM) surgery. Excessive mechanical stress increases Piezo1 in chondrocytes, which leads to a reduction in collagen II (COL2) and aggrecan (ACAN). In addition, activation of Piezo1 channels by the specific agonist Yoda1 reduces chondrocyte anabolism and promotes catabolism. Molecularly, activation or inhibition of Piezo1 modulates the activity of the PI3K/AKT/mTORC1 pathway. Inhibition of the PI3K/AKT pathway or mTORC1 alleviated the Yoda1-induced imbalance of chondrocyte homeostasis to varying degrees. Collectively, these findings imply that Piezo1 in chondrocytes may respond to excessive mechanical forces and promote extracellular matrix degradation through the PI3K/AKT/mTORC1 pathway, thereby driving OA progression.

Indexed as

ChondrocytesHomeostasisIon ChannelsMechanistic Target of Rapamycin Complex 1Mechanotransduction, CellularOsteoarthritisPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktAnimalsCartilage, ArticularExtracellular MatrixMaleRatsRats, Sprague-DawleySignal TransductionStress, MechanicalIon ChannelsMechanistic Target of Rapamycin Complex 1Phosphatidylinositol 3-KinasesPiezo1 protein, ratProto-Oncogene Proteins c-aktchondrocyte homeostasismechanical stressmTORC1osteoarthritisPI3K/AKTPiezo1

Identifiers

PMID40745673
PMCPMC12313542

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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.