Evidence map›Paper›PMID 38552635›Full record

ArticleStem cell reports2024

MST1/2 regulates fibro/adipogenic progenitor fate decisions in skeletal muscle regeneration.

Kezhi Wang, Jingjing Yang, Yina An, Jing Wang, Shuyu Tan, Hui Xu, Yanjun Dong

Abstract read
In one paragraph

Article in Stem cell reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  9. Review
  10. Intramuscular adipose tissue: from progenitor to pathology.American journal of physiology. Cell physiology · 2025
    Review
  11. Review
  12. Article
  13. 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

7 authors.

Kezhi WangCollege of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Jingjing YangCollege of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Yina AnCollege of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Jing WangCollege of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Shuyu TanCollege of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Hui XuDepartment of Physical Education, China Agricultural University, Beijing 100193, China. Electronic address: xuhui@cau.edu.cn.
Yanjun DongCollege of Veterinary Medicine, China Agricultural University, Beijing 100193, China. Electronic address: yanjund@cau.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Defective skeletal muscle regeneration is often accompanied by fibrosis. Fibroblast/adipose progenitors (FAPs) are important in these processes, however, the regulation of FAP fate decisions is unclear. Here, using inducible conditional knockout mice, we show that blocking mammalian Ste20-like kinases 1/2 (MST1/2) of FAPs prevented apoptosis and reduced interleukin-6 secretion in vivo and in vitro, which impaired myoblast proliferation and differentiation, as well as impaired muscle regeneration. Deletion of Mst1/2 increased co-localization of Yes-associated protein (YAP) with Smad2/3 in nuclei and promoted differentiation of FAPs toward myofibroblasts, resulting in excessive collagen deposition and skeletal muscle fibrosis. Meanwhile, inhibition of MST1/2 increased YAP/Transcriptional co-activator with PDZ-binding motif activation, which promoted activation of the WNT/β-catenin pathway and impaired the differentiation of FAPs toward adipocytes. These results reveal a new mechanism for MST1/2 action in disrupted skeletal muscle regeneration and fibrosis via regulation of FAP apoptosis and differentiation. MST1/2 is a potential therapeutic target for the treatment of some myopathies.

Indexed as

AdipocytesAdipogenesisAnimalsCell DifferentiationFibrosisMammalsMiceMuscle, SkeletalapoptosisdifferentiationFAPsIL-6MST1/2YAP

Identifiers

PMID38552635
PMCPMC11096422

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.