Evidence map›Paper›PMID 36151111›Full record

ArticleScientific reports2022

Actin cable formation and epidermis-dermis positional relationship during complete skin regeneration.

Kento Takaya, Keisuke Okabe, Ayaka Ishigami, Yuka Imbe, Hideko Kanazawa, Shigeki Sakai, Noriko Aramaki-Hattori, Kazuo Kishi

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 20 citations in OpenAlex.

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  18. Dendritic Cell-Associated MARCKSL1 Regulates Fibroblast Differentiation During Wound Healing.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    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

8 authors at 1 institution in 1 country.

Kento TakayaDepartment of Plastic and Reconstructive Surgery, School of Medicine, Keio University, 35 Shinanomachi, Shinjukuku, Tokyo, 160-8582, Japan.
Keisuke OkabeDepartment of Plastic and Reconstructive Surgery, School of Medicine, Keio University, 35 Shinanomachi, Shinjukuku, Tokyo, 160-8582, Japan.
Ayaka IshigamiFaculty of Pharmacy, Keio University, Shiba, Minatoku, Tokyo, Japan.
Yuka ImbeFaculty of Pharmacy, Keio University, Shiba, Minatoku, Tokyo, Japan.
Hideko KanazawaFaculty of Pharmacy, Keio University, Shiba, Minatoku, Tokyo, Japan.
Shigeki SakaiDepartment of Plastic and Reconstructive Surgery, School of Medicine, Keio University, 35 Shinanomachi, Shinjukuku, Tokyo, 160-8582, Japan.
Noriko Aramaki-HattoriDepartment of Plastic and Reconstructive Surgery, School of Medicine, Keio University, 35 Shinanomachi, Shinjukuku, Tokyo, 160-8582, Japan.
Kazuo KishiDepartment of Plastic and Reconstructive Surgery, School of Medicine, Keio University, 35 Shinanomachi, Shinjukuku, Tokyo, 160-8582, Japan. kkishi@keio.jp.
Keio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Up to a certain developmental stage, a fetus can completely regenerate wounds in the skin. To clarify the mechanism of fetal skin regeneration, identifying when the skin switches from fetal-type wound regeneration to adult-type wound repair is necessary. We hypothesized that this switch occurs at several time points and that complete skin regeneration requires epidermal-dermal interactions and the formation of actin cables. We compared normal skin and wound morphology at each developmental stage. We examined two parameters: epidermal texture and dermal structure. We found that the three-dimensional structure of the skin was completely regenerated in full-thickness skin incisions made before embryonic day (E) 13. However, the skin texture did not regenerate in wounds made after E14. We also found that the dermal structure regenerates up to E16, but wounds created after E17 heal as scars with dermal fibrosis. By controlling the activity of AMP-activated protein kinase and altering actin cable formation, we could regulate scar formation in utero. These findings may contribute to therapies that allow complete skin regeneration without scarring.

Indexed as

ActinsAMP-Activated Protein KinasesRegenerationSkinAnimalsCicatrixDermisEpidermisFetusMiceActinsAMP-Activated Protein Kinases

Identifiers

PMID36151111
PMCPMC9508246
OpenAlexW4296841178

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.