Evidence map›Paper›PMID 36373718›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2022

Cilia-Mediated Insulin/Akt and ST2/JNK Signaling Pathways Regulate the Recovery of Muscle Injury.

Daishi Yamakawa, Junya Tsuboi, Kousuke Kasahara, Chise Matsuda, Yuhei Nishimura, Tatsuya Kodama, Naoyuki Katayama, Masatoshi Watanabe, Masaki Inagaki

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2022. 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
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Primary cilia dysfunction: A critical driver of metabolic diseases (Review).International journal of molecular medicine · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. The role of JNK signaling pathway in organ fibrosis.Journal of advanced research · 2025
    Review
  7. Article
  8. The Primary Cilia are Associated with the Axon Initial Segment in Neurons.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  9. PdgfrαGenes & diseases · 2025
    Review
  10. Article
  11. Primary cilia support cartilage regeneration after injury.International journal of oral science · 2023
    Article
  12. Review
  13. 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

9 authors at 1 institution in 1 country.

Daishi YamakawaDepartment of Physiology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.
Junya TsuboiDepartment of Gastroenterology and Hepatology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.
Kousuke KasaharaDepartment of Physiology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.
Chise MatsudaDepartment of Oncogenic Pathology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.
Yuhei NishimuraDepartment of Integrative Pharmacology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.
Tatsuya KodamaDepartment of Physiology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.
Naoyuki KatayamaDepartment of Hematology and Oncology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.
Masatoshi WatanabeDepartment of Oncogenic Pathology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.
Masaki InagakiDepartment of Physiology, Mie University Graduate School of Medicine, Tsu, Mie, 514-8507, Japan.ORCID https://orcid.org/0000-0002-7742-3314
Mie University · JP

Funding

Aichi Health Promotion FoundationJapan Society for the Promotion of Science KAKENHI 19K07318Japan Society for the Promotion of Science KAKENHI 20H03448Japan Society for the Promotion of Science KAKENHI 20K07356Japan Society for the Promotion of Science KAKENHI 21H02696Naito FoundationNakatomi FoundationTakeda Science FoundationUehara Memorial Foundation
6 · The paper itself

Abstract

Following injury, skeletal muscle regenerates but fatty tissue accumulation is seen in aged muscle or muscular dystrophies. Fibro/adipogenic progenitors (FAPs) are key players in these events; however, the effect of primary cilia on FAPs remains unclear. Here, it is reported that genetic ablation of trichoplein (TCHP), a ciliary regulator, induces ciliary elongation on FAPs after injury, which promotes muscle regeneration while inhibiting adipogenesis. The defective adipogenic differentiation of FAPs is attributed to dysfunction of cilia-dependent lipid raft dynamics, which is critical for insulin/Akt signaling. It is also found that interleukin (IL) 13 is substantially produced by intramuscular FAPs, which are upregulated by ciliary elongation and contribute to regeneration. Mechanistically, upon injury, long cilia excessively activate the IL33/ST2/JNK axis to enhance IL13 production, facilitating myoblast proliferation and M2 macrophage polarization. The results indicate that FAPs organize the regenerative responses to skeletal muscle injury via cilia-mediated insulin/Akt and ST2/JNK signaling pathways.

Indexed as

adipogenesisfibro/adipogenic progenitorsinterleukin 13interleukin 33lipid raftprimary ciliaskeletal muscle regeneration

Identifiers

PMID36373718
PMCPMC9811445
OpenAlexW4308953971

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.