Evidence map›Paper›PMID 38335719›Full record

ArticleBiomaterials2024

Stiffness assisted cell-matrix remodeling trigger 3D mechanotransduction regulatory programs.

Anna L Kersey, Daniel Y Cheng, Kaivalya A Deo, Christina R Dubell, Ting-Ching Wang, Manish K Jaiswal, Min Hee Kim, Aparna Murali, Sarah E Hargett, Sumana Mallick and 3 more

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
13.0field-weighted citation impact, top 1% of its field
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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  13. The Rise of Mechanobiology for Advanced Cell Engineering and Manufacturing.Advanced materials (Deerfield Beach, Fla.) · 2025
    Review
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  19. Article
  20. Inorganic Biomaterials Shape the Transcriptome Profile to Induce Endochondral Differentiation.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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

13 authors at 2 institutions in 1 country.

Anna L KerseyDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Daniel Y ChengDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Kaivalya A DeoDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Christina R DubellDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Ting-Ching WangDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Manish K JaiswalDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Min Hee KimDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Aparna MuraliDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Sarah E HargettDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Sumana MallickDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA; Department of Cell Biology and Genetics, School of Medicine, Texas A&M University, Bryan, TX 77807, USA.
Tanmay P LeleDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA.
Irtisha SinghDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA; Department of Cell Biology and Genetics, School of Medicine, Texas A&M University, Bryan, TX 77807, USA; Interdisciplinary Program in Genetics, Texas A&M University, College Station, TX 77843, USA. Electronic address: isingh@tamu.edu.
Akhilesh K GaharwarDepartment of Biomedical Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA; Interdisciplinary Program in Genetics, Texas A&M University, College Station, TX 77843, USA; Center for Remote Health Technologies and Systems, Texas A&M University, College Station, TX 77843, USA; Department of Material Science and Engineering, College of Engineering, Texas A&M University, College Station, TX 77843, USA. Electronic address: gaharwar@tamu.edu.
Texas A&M University · USTexas A&M Health Science Center · US

Funding

Nuclear Dysfunction in Cancer: The Role of Mechanical Stresses Transmittedby the LINC ComplexU01CA225566 · NCI · UNIVERSITY OF FLORIDA · PI LELE, TANMAY P. · 2020 to 2024
$3.1M
Mineralomics: Designing mineral based therapeutics to control and direct cell functionDP2EB026265 · NIBIB · TEXAS ENGINEERING EXPERIMENT STATION · PI GAHARWAR, AKHILESH K. · 2017 to 2021
$2.4M
Investigating Pathophysiology of Glioma Stem Cells in 3D Bioprinted Vascularized Glioblastoma ModelR21NS121945 · NINDS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SINGH, IRTISHA · 2022 to 2023
$403k
NCI NIH HHS U01 CA225566NIBIB NIH HHS DP2 EB026265NINDS NIH HHS R21 NS121945
6 · The paper itself

Abstract

Engineered matrices provide a valuable platform to understand the impact of biophysical factors on cellular behavior such as migration, proliferation, differentiation, and tissue remodeling, through mechanotransduction. While recent studies have identified some mechanisms of 3D mechanotransduction, there is still a critical knowledge gap in comprehending the interplay between 3D confinement, ECM properties, and cellular behavior. Specifically, the role of matrix stiffness in directing cellular fate in 3D microenvironment, independent of viscoelasticity, microstructure, and ligand density remains poorly understood. To address this gap, we designed a nanoparticle crosslinker to reinforce collagen-based hydrogels without altering their chemical composition, microstructure, viscoelasticity, and density of cell-adhesion ligand and utilized it to understand cellular dynamics. This crosslinking mechanism utilizes nanoparticles as crosslink epicenter, resulting in 10-fold increase in mechanical stiffness, without other changes. Human mesenchymal stem cells (hMSCs) encapsulated in 3D responded to mechanical stiffness by displaying circular morphology on soft hydrogels (5 kPa) and elongated morphology on stiff hydrogels (30 kPa). Stiff hydrogels facilitated the production and remodeling of nascent extracellular matrix (ECM) and activated mechanotransduction cascade. These changes were driven through intracellular PI3AKT signaling, regulation of epigenetic modifiers and activation of YAP/TAZ signaling. Overall, our study introduces a unique biomaterials platform to understand cell-ECM mechanotransduction in 3D for regenerative medicine as well as disease modelling.

Indexed as

Mechanotransduction, CellularMesenchymal Stem CellsCollagenExtracellular MatrixHumansHydrogelsLigandsCollagenHydrogelsLigandsBiomaterialsDisease modellingMechanotransductionRegenerative medicineThree-dimensional (3D) microenvironment

Identifiers

PMID38335719
PMCPMC12861118
OpenAlexW4390976901

What OpenQuestion holds

Textmetadata
LicenceTDM
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.