Evidence map›Paper›PMID 40821896›Full record

ArticlePlastic and reconstructive surgery. Global open2025

Novel Concept of "Right-at-the-right-place" Transplantation: Rejuvenating Effects of Mouse Fascial Fibroblasts.

Ryoga Wake, Kento Takaya, Rikako Matsuura, Shigeki Sakai, Keisuke Okabe, Noriko Aramaki-Hattori, Kazuo Kishi

Abstract read
In one paragraph

Article in Plastic and reconstructive surgery. Global open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ryoga WakeFrom the Department of Plastic and Reconstructive Surgery, Keio University School of Medicine, Tokyo, Japan.
Kento TakayaFrom the Department of Plastic and Reconstructive Surgery, Keio University School of Medicine, Tokyo, Japan.
Rikako MatsuuraFrom the Department of Plastic and Reconstructive Surgery, Keio University School of Medicine, Tokyo, Japan.
Shigeki SakaiFrom the Department of Plastic and Reconstructive Surgery, Keio University School of Medicine, Tokyo, Japan.
Keisuke OkabeFrom the Department of Plastic and Reconstructive Surgery, Keio University School of Medicine, Tokyo, Japan.
Noriko Aramaki-HattoriFrom the Department of Plastic and Reconstructive Surgery, Keio University School of Medicine, Tokyo, Japan.
Kazuo KishiFrom the Department of Plastic and Reconstructive Surgery, Keio University School of Medicine, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Live autologous cultured fibroblasts improve sagging and wrinkles when injected into the dermis; however, their diversity and differences in efficacy depending on the skin layer to which they are transplanted remain unclear. This study investigated the behavior and effects of dermal- and fascial-derived fibroblasts from mouse fetuses on the dermis and fascia. Methods: The collagen-producing capacity of fibroblasts from the shallow (dermis) and deep (fascia) skin layers of fetal and adult C57BL/6-Tg(CAG-EGFP) mice was compared using western blotting and real-time polymerase chain reaction. Contractile capacity was investigated using a collagen contractility assay and an ex vivo mouse skin model. We transplanted these cells into the shallow and deep layers of the back skin of aged C57BL/6 mice and observed the engraftment rate and histological changes in the skin. The anti-inflammatory effects of these cells were also compared. Results: Fascial fibroblasts from embryonic day 17 fetal mice exhibited higher collagen production and contractile capacity than papillary fibroblasts from adult mice. The transplanted fascial and dermal cells showed high engraftment rates in the deep and shallow (injected near the layer from which they were derived) layers, respectively. Collagen fiber density was highest when embryonic day 17 fascial fibroblasts were transplanted into the deep layer, and an anti-inflammatory effect was observed. Conclusions: Dermal fibroblast transplantation improves the phenotype of aging skin via collagen synthesis and contraction, with greater efficacy when transplanted into a layer consistent with the skin layer from which the primary cells are harvested.

Identifiers

PMID40821896
PMCPMC12356635

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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.