Evidence map›Paper›PMID 37888610›Full record

ArticleInternational journal of molecular medicine2023

Exosomes derived from human dermal fibroblasts protect against UVB‑induced skin photoaging.

A Yeon Park, Jung Ok Lee, Youna Jang, Yu-Jin Kim, Jung Min Lee, Su-Young Kim, Beom Joon Kim, Kwang Ho Yoo

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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  13. Plant-derived extracellular vesicles in facial aesthetics.Extracellular vesicles and circulating nucleic acids · 2025
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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

8 authors at 1 institution in 1 country.

A Yeon ParkDepartment of Dermatology, College of Medicine, Chung‑Ang University, Seoul 06974, Republic of Korea.
Jung Ok LeeDepartment of Dermatology, College of Medicine, Chung‑Ang University, Seoul 06974, Republic of Korea.
Youna JangDepartment of Dermatology, College of Medicine, Chung‑Ang University, Seoul 06974, Republic of Korea.
Yu-Jin KimDepartment of Dermatology, College of Medicine, Chung‑Ang University, Seoul 06974, Republic of Korea.
Jung Min LeeDepartment of Dermatology, College of Medicine, Chung‑Ang University, Seoul 06974, Republic of Korea.
Su-Young KimDepartment of Dermatology, College of Medicine, Chung‑Ang University, Seoul 06974, Republic of Korea.
Beom Joon KimDepartment of Dermatology, College of Medicine, Chung‑Ang University, Seoul 06974, Republic of Korea.
Kwang Ho YooDepartment of Dermatology, Chung‑Ang University Gwang‑Myeong Hospital, Chung‑Ang University College of Medicine, Gwangmyeong‑si, Gyeonggi‑do 14353, Republic of Korea.
Chung-Ang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes are used as innovative treatment options for repairing skin defects, such as aging, atopic dermatitis and wounds. However, the effects of exosomes obtained from human foreskin fibroblasts BJ‑5ta (BJ‑5ta Exo) on ultraviolet B (UVB)‑mediated photoaging have not been previously reported, at least to the best of our knowledge. Therefore, the present study aimed to investigate the anti‑photoaging effects of BJ‑5ta Exo on UVB radiation in human skin fibroblasts and SKH‑1 hairless mice. The results revealed that BJ‑5ta Exo decreased the production of reactive oxygen species and inhibited the decrease in the expression levels of superoxide dismutase 1 and 2, glutathione peroxidase and catalase following UVB exposure. In addition, BJ‑5ta Exo attenuated the decrease in nuclear factor erythroid 2‑related factor 2 levels induced by UVB rays, indicating its scavenging activity against oxidative stress. Moreover, BJ‑5ta Exo inhibited the UVB‑induced increase in the levels of γH2AX, p53/21 and cleaved PARP, whereas it promoted DNA double‑strand break repair through radiation sensitive 52 and effectively activated the TGF‑β1/Smad pathway. BJ‑5ta Exo also protected against UVB‑induced senescence, as indicated by the downregulation in the levels of senescence‑associated β‑galactosidase and p16. In a mouse model of photoaging, BJ‑5ta Exo prevented the UVB‑induced increase in transepidermal water loss, wrinkle formation and MMP‑1 expression, while also suppressing the UVB‑mediated decrease in collagen type I and elastin levels in the dorsal skin. Overall, the findings of the present study suggest that BJ‑5ta Exo represent an effective anti‑photoaging agent, which can be used as a component in cosmetic products.

Indexed as

ExosomesSkin AgingAnimalsCollagen Type IFibroblastsHumansMiceReactive Oxygen SpeciesSkinUltraviolet RaysCollagen Type IReactive Oxygen SpeciesBJ‑5ta fibroblastDNA damageexosomeoxidative stressROSskin photoagingUVB

Identifiers

PMID37888610
PMCPMC10635689
OpenAlexW4387966590

What Socratic holds

Textmetadata
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 Socratic graph.