Evidence map›Paper›PMID 42627293›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Application and Single-Cell Regulation Mechanism of Engineered EVs Combined With 4D-Printed Hydrogel for Infected Burn Repair.

Xiaomin Wang, Xiaoyan Li, Xiao Xu, Kelun Zhang, Fengjiao Yu, Zhen Shang, Nailong Pan, Junlin Lv, Yiwei Xu, Yan Tang and 10 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. 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

20 authors.

Xiaomin WangInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.ORCID https://orcid.org/0000-0002-3627-6936
Xiaoyan LiInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Xiao XuInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Kelun ZhangDepartment of Dermatology and Cutaneous Biology Research Institute, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.ORCID https://orcid.org/0000-0003-1387-7373
Fengjiao YuInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Zhen ShangInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Nailong PanInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.ORCID https://orcid.org/0009-0002-4856-0763
Junlin LvInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.ORCID https://orcid.org/0000-0003-1359-0057
Yiwei XuInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Yan TangInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Liang ZhangInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Xiaotong LiInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.ORCID https://orcid.org/0009-0005-4791-1842
Taoyi WangInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Jing TaoInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Jiaxu SongInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Mengyu ZhangInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Xin MaInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Dan HanInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.
Xiaoying KongInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.ORCID https://orcid.org/0000-0001-9326-6171
Wenhua XuInstitute of Regenerative Medicine and Laboratory Technology Innovation, Qingdao University, Qingdao, Shandong, P. R. China.ORCID https://orcid.org/0000-0001-7426-6950

Funding

Horizontal Major Projects in Shandong Province RH2200000157Key Projects of Qingdao Science and Technology Department 20-3-4-43-nshMarine Pilot Laboratory of Ministry of Science and Technology 10-02National Key Research and Development Program 2022YEF0132500National Natural Science Foundation of China 32101137National Natural Science Foundation of China 81770900National Natural Science Foundation of China 82302653Qingdao Natural Science Foundation 24-4-4-zrjj-150-jchShandong Provincial Major Basic Research Project ZR2026ZD35Shandong Taishan scholars special expert project tstp20240824
6 · The paper itself

Abstract

Burns represent a complex and disabling global public health problem, presenting substantial clinical challenges attributed to disrupted tissue microenvironment and persistent wound infections, which impair the synergistic interaction between fibroblasts (Fb) and keratinocytes (KC). FGF2 and its homologues widely used for burns show weak wound-repair efficacy, owing to poor targeting and degradation by bacteria and proteases. In this study, FGF2-modified extracellular vesicles (F-EVs) were engineered from human adipose mesenchymal stem cells (ADMSCs) via electrostatic adsorption, and further combined with 4D-printed hydrogels to construct a 4D@F-EVs system. This system was designed to reconstruct the burn tissue microenvironment, exert antibacterial effects, and restore the crosstalk between Fb and KC. In vitro and in vivo analysis confirmed that the 4D@F-EVs were precisely delivered to Fb, promoting cell proliferation and facilitating the reconstruction of the burn tissue microenvironment. Single-cell RNA sequencing (scRNA-seq) analysis revealed that the regulatory effect of 4D@F-EVs on skin regeneration involves the activation of the PI3K-Akt signaling pathway and the promotion of crosstalk between Keratinocyte Growth Factor-positive (KGF

Indexed as

4D biopritingburnscells crosstalkengineered EVsFGF2

Identifiers

PMID42627293
PMCPMC13496149

What OpenQuestion holds

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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.