Evidence map›Paper›PMID 33597503›Full record

ArticleCell death discovery2021

Dexamethasone accelerates muscle regeneration by modulating kinesin-1-mediated focal adhesion signals.

Jong-Wei Lin, Yi-Man Huang, Yin-Quan Chen, Ting-Yun Chuang, Tien-Yun Lan, Yen-Wenn Liu, Hung-Wei Pan, Li-Ru You, Yang-Kao Wang, Keng-Hui Lin and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

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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

12 authors at 4 institutions in 1 country.

Jong-Wei LinInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Yi-Man HuangInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Yin-Quan ChenCancer Progression Research Center, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Ting-Yun ChuangInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Tien-Yun LanInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Yen-Wenn LiuInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Hung-Wei PanSchool of Medicine for International Students, College of Medicine, I-Shou University, Kaohsiung, 82445, Taiwan.
Li-Ru YouInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Yang-Kao WangDepartment of Cell Biology and Anatomy, College of Medicine, National Cheng Kung University, Tainan, 70101, Taiwan.
Keng-Hui LinInstitute of Physics, Academia Sinica, Taipei, 11529, Taiwan.
Arthur ChiouInstitute of Biophotonics, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan.
Jean-Cheng KuoInstitute of Biochemistry and Molecular Biology, National Yang Ming Chiao Tung University, Hsinchu, 30010, Taiwan. jckuo@nycu.edu.tw.ORCID http://orcid.org/0000-0003-3682-0783
National Yang Ming Chiao Tung University · TWInstitute of Physics, Academia Sinica · TWI-Shou University · TWNational Cheng Kung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During differentiation, skeletal muscle develops mature multinucleated muscle fibers, which could contract to exert force on a substrate. Muscle dysfunction occurs progressively in patients with muscular dystrophy, leading to a loss of the ability to walk and eventually to death. The synthetic glucocorticoid dexamethasone (Dex) has been used therapeutically to treat muscular dystrophy by an inhibition of inflammation, followed by slowing muscle degeneration and stabilizing muscle strength. Here, in mice with muscle injury, we found that Dex significantly promotes muscle regeneration via promoting kinesin-1 motor activity. Nevertheless, how Dex promotes myogenesis through kinesin-1 motors remains unclear. We found that Dex directly increases kinesin-1 motor activity, which is required for the expression of a myogenic marker (muscle myosin heavy chain 1/2), and also for the process of myoblast fusion and the formation of polarized myotubes. Upon differentiation, kinesin-1 mediates the recruitment of integrin β1 onto microtubules allowing delivery of the protein into focal adhesions. Integrin β1-mediated focal adhesion signaling then guides myoblast fusion towards a polarized morphology. By imposing geometric constrains via micropatterns, we have proved that cell adhesion is able to rescue the defects caused by kinesin-1 inhibition during the process of myogenesis. These discoveries reveal a mechanism by which Dex is able to promote myogenesis, and lead us towards approaches that are more efficient in improving skeletal muscle regeneration.

Identifiers

PMID33597503
PMCPMC7889929
OpenAlexW3131960503

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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.