Evidence map›Paper›PMID 39903386›Full record

ArticleJournal of molecular histology2025

The role of RAP2 in regulation of cell volume on bone marrow mesenchymal stem cell fate determination.

Yimei Zhou, Yutong Guo, Mei Zhang, Shuqi Quan, Juan Li

Abstract read
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Article in Journal of molecular histology, 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

5 authors.

Yimei ZhouState Key Laboratory of Oral Diseases, National Center of Stomatology, West China Hospital of Stomatology, National Clinical Research Center for Oral Diseases, Sichuan University, 14#, 3rd Section, Renmin South Road, Chengdu, 610041, China.
Yutong GuoDepartment of Orthodontics, National Center for Stomatology, National Clinical Research Center for Oral Diseases, National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, Beijing Key Laboratory of Digital Stomatology, Peking University School and Hospital of Stomatology, Research Center of Engineering and Technology for Computerized Dentistry Ministry of Health, Beijing, 100081, PR China.
Mei ZhangState Key Laboratory of Oral Diseases, National Center of Stomatology, West China Hospital of Stomatology, National Clinical Research Center for Oral Diseases, Sichuan University, 14#, 3rd Section, Renmin South Road, Chengdu, 610041, China.
Shuqi QuanState Key Laboratory of Oral Diseases, National Center of Stomatology, West China Hospital of Stomatology, National Clinical Research Center for Oral Diseases, Sichuan University, 14#, 3rd Section, Renmin South Road, Chengdu, 610041, China.
Juan LiState Key Laboratory of Oral Diseases, National Center of Stomatology, West China Hospital of Stomatology, National Clinical Research Center for Oral Diseases, Sichuan University, 14#, 3rd Section, Renmin South Road, Chengdu, 610041, China. lijuan@scu.edu.cn.

Funding

Interdisciplinary Innovation Project from West China Hospital of Stomatology, Sichuan University RD-03-202305National Natural Science Foundation of China 32271364
6 · The paper itself

Abstract

The extracellular matrix guides cell behavior through mechanical properties, which plays a role in determining cell function and can even influence stem cell fate. Compared with adherent culture, the three-dimensional culture environment is closer to the growth conditions in vivo, but is limited by standardization of material properties and observation and measurement methods. Therefore, it is necessary to study the relationship among the three-dimensional morphological characteristics of cells, cytoskeleton, and stem cell differentiation under adherent culture conditions. Here, we control the cell volume by adjusting the cell density, microfilament cytoskeleton tension, and osmotic pressure of the culture environment, and analyze the cell morphological features and differentiation to the osteoblastic and adipogenic lineages. Based on the in vitro and in vivo results, we identify cell volume as the true reflection of the cytoskeleton tension under stress stimuli compared with cell spreading area. By adjusting cell volume, cytoskeletal tension and cell differentiation can be regulated without affecting cell spreading area. Further study shows that the Ras-related small GTPase RAP2 inhibits the activity of mechanical transducers Lamin A/C and YAP1, playing an important role in cell volume regulation of cell differentiation. In summary, our results support the close relationship between cell volume and cytoskeleton tension. The regulatory role of cell volume on cell differentiation is modulated, at least in part, by RAP2-related mechanosensitive pathways. Our insights into how cell volume regulates cell differentiation may build a bridge between two-dimensional and three-dimensional mechanical studies in cell biology.

Indexed as

Bone Marrow CellsCell DifferentiationCell LineageCell SizeMesenchymal Stem Cellsrap GTP-Binding ProteinsAnimalsCells, CulturedCytoskeletonMiceOsteoblastsrap GTP-Binding ProteinsCell mechanicsCell volumeRAP2AStem cell fate

Identifiers

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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.