Evidence map›Paper›PMID 39882542›Full record

ArticleResearch (Washington, D.C.)2023

Cell Mechanics Regulates the Dynamic Anisotropic Remodeling of Fibril Matrix at Large Scale.

Mingxing Ouyang, Yanling Hu, Weihui Chen, Hui Li, Yingbo Ji, Linshuo Qiu, Linlin Zhu, Baohua Ji, Bing Bu, Linhong Deng

Abstract read
In one paragraph

Article in Research (Washington, D.C.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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.

Mingxing OuyangInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.ORCID https://orcid.org/0000-0002-2910-0713
Yanling HuInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.
Weihui ChenInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.
Hui LiInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.
Yingbo JiInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.
Linshuo QiuInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.
Linlin ZhuInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.
Baohua JiInstitute of Biomechanics and Applications, Department of Engineering Mechanics, Zhejiang University, Hangzhou, 310027, China.ORCID https://orcid.org/0000-0002-0092-6562
Bing BuInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.
Linhong DengInstitute of Biomedical Engineering and Health Sciences, School of Medical and Health Engineering and School of Pharmacy, Changzhou University, Changzhou, 213164, China.ORCID https://orcid.org/0000-0003-1970-8239

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Living tissues often have anisotropic and heterogeneous organizations, in which developmental processes are coordinated by cells and extracellular matrix modeling. Cells have the capability of modeling matrix in long distance; however, the biophysical mechanism is largely unknown. We investigated the dynamic remodeling of collagen I (COL) fibril matrix by cell contraction with designed patterns of cell clusters. By considering cell dynamic contractions, our molecular dynamics simulations predicted the anisotropic patterns of the observed COL bundling in experiments with various geometrical patterns without spatial limitation. The pattern of COL bundling was closely related to the dynamic remodeling of fibril under cell active contraction. We showed that cell cytoskeletal integrity (actin filaments and microtubules), actomyosin contractions, and endoplasmic reticulum calcium channels acting as force generations and transductions were essential for fiber bundling inductions, and membrane mechanosensory components integrin and Piezo played critical roles as well. This study revealed the underlying mechanisms of the cell mechanics-induced matrix remodeling in large scales and the associated cellular mechanism and should provide important guidelines for tissue engineering in potential biomedical applications.

Identifiers

PMID39882542
PMCPMC11776286

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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.