Evidence map›Paper›PMID 41155127›Full record

ArticleBioengineering (Basel, Switzerland)2025

Exosomes from Adipose Tissue Mesenchymal Stem Cells, a Preliminary Study for In Vitro and In Vivo Application.

Thao Duy Huynh, Ciro Gargiulo Isacco, Quan Thai Minh Ngo, Binh Thanh Nguyen, Tuan Ngoc Huu Nguyen, Tri Minh Dang Bui, Vinh Minh Ngo, Ky Quoc Truong, Tro Van Chau, Hoa Cong Truong and 5 more

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 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
–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

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

15 authors.

Thao Duy HuynhBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.ORCID 0000-0001-5397-8000
Ciro Gargiulo IsaccoInterdisciplinary Department of Medicine, Section of Microbiology and Virology, School of Medicine, The University of Bari, 70124 Bari, Italy.
Quan Thai Minh NgoBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.
Binh Thanh NguyenBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.
Tuan Ngoc Huu NguyenBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.ORCID 0009-0009-0635-7979
Tri Minh Dang BuiBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.
Vinh Minh NgoBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.ORCID 0000-0003-3513-9822
Ky Quoc TruongBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.
Tro Van ChauBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.
Hoa Cong TruongBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.
Kieu Diem Cao NguyenThe Institute of Immunology, Gene, and Cell Therapy, Hanoi City 100000, Vietnam.
Emilio JirilloInterdisciplinary Department of Medicine, Section of Microbiology and Virology, School of Medicine, The University of Bari, 70124 Bari, Italy.
Van Hung PhamViet Nam Research and Development Institute of Clinical Microbiology, Ho Chi Minh City 756000, Vietnam.ORCID 0000-0002-1672-3292
Luigi SantacroceInterdisciplinary Department of Medicine, Section of Microbiology and Virology, School of Medicine, The University of Bari, 70124 Bari, Italy.ORCID 0000-0001-5671-8124
Toai Cong TranBiomedical Research Center, Pham Ngoc Thac University of Medicine, Ho Chi Minh City 700000, Vietnam.ORCID 0000-0001-5722-8581

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs), particularly their secreted exosomes, small microvesicles, represent a major focus in regenerative medicine due to their therapeutic potential. Exosomes exhibit growth factors and cytokines and are loaded with microRNAs (miRNA) and short interfering RNA (siRNA) that can be transferred to other cells, potentially affecting their function. Exosomes are crucial mediators of intercellular communication, are immunomodulatory, and are promoters of tissue regeneration. Despite their promise, the standardized methods for exosome isolation and characterization remain weak. This exploratory study addresses this gap by detailing an effective method for isolating exosomes from adipose tissue mesenchymal stem cells (AT-MSCs), emphasizing precipitation as a technique yielding a high efficiency and purity compared to other methods. Functionally, we aimed to confirm the AT-MSC exosomes' ability to exert an effective protective activity on the skin and its main components, such as fibroblasts, collagen, and elastin. To achieve this goal, we had to demonstrate that AT-MSC exosomes are safe and free of toxic substances. They can express specific proteins such as CD9, CD63, and CD81, which are well-known exosome markers. These exosomes also contain key miRNAs, including miRNA-203 A, miRNA-203 B, and miRNA-3196, important for skin regeneration, as well as enhancers of cell integrity and proliferation. We eventually confirmed the ability of exosomes to exert protective and recovery effects on fibroblasts after H

Indexed as

adipose tissue mesenchymal stem cells (AT-MSCs)exosomesH2O2-induced damagemiRNAqRT-PCRsiRNAUVB-induced damage

Identifiers

PMID41155127
PMCPMC12561650

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Registered trials

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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.