Evidence map›Paper›PMID 36176601›Full record

ArticleBioengineering & translational medicine2022

Biofabricated macrophage and fibroblast membranes synergistically promote skin wound healing.

Dongqing Wang, Heying Chen, Li Lei, Jun Chen, Jimin Gao, Jiahe Liu, Qianyin Li, Yajun Xie, Yi Hu, Yilu Ni

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
  6. Article
  7. Article
  8. Advances in Zebrafish for Diabetes Mellitus with Wound Model.Bioengineering (Basel, Switzerland) · 2023
    Review
  9. Article
  10. Article
  11. 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

10 authors at 3 institutions in 1 country.

Dongqing WangThe M.O.E. Key Laboratory of Laboratory Medical Diagnostics, The College of Laboratory Medicine Chongqing Medical University Yuzhong District Chongqing China.ORCID https://orcid.org/0000-0002-1941-3732
Heying ChenThe M.O.E. Key Laboratory of Laboratory Medical Diagnostics, The College of Laboratory Medicine Chongqing Medical University Yuzhong District Chongqing China.
Li LeiThe M.O.E. Key Laboratory of Laboratory Medical Diagnostics, The College of Laboratory Medicine Chongqing Medical University Yuzhong District Chongqing China.
Jun ChenCAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety Institute of High Energy Physics and University of Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS) Beijing China.
Jimin GaoZhejiang Provincial Key Laboratory for Technology & Application of Model Organisms, School of Laboratory Medicine and Life Science Wenzhou Medical University, University Town Wenzhou Zhejiang China.
Jiahe LiuThe M.O.E. Key Laboratory of Laboratory Medical Diagnostics, The College of Laboratory Medicine Chongqing Medical University Yuzhong District Chongqing China.
Qianyin LiThe M.O.E. Key Laboratory of Laboratory Medical Diagnostics, The College of Laboratory Medicine Chongqing Medical University Yuzhong District Chongqing China.
Yajun XieThe M.O.E. Key Laboratory of Laboratory Medical Diagnostics, The College of Laboratory Medicine Chongqing Medical University Yuzhong District Chongqing China.
Yi HuCAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety Institute of High Energy Physics and University of Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS) Beijing China.ORCID https://orcid.org/0000-0002-0952-0657
Yilu NiThe M.O.E. Key Laboratory of Laboratory Medical Diagnostics, The College of Laboratory Medicine Chongqing Medical University Yuzhong District Chongqing China.ORCID https://orcid.org/0000-0002-0402-4734
Chongqing Medical University · CNInstitute of High Energy Physics · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective skin wound healing is a complex process involving anti-inflammation, fibrosis, matrix reconstruction, and angiogenesis. This work aimed to integrate the macrophage-mediated anti-inflammation and fibroblast-assisted matrix reconstruction for enhanced skin wound healing. Herein, we utilized the cytomembranes derived from repolarized M2 macrophages and fibroblasts to prepare the natural biologics. Results showed that the inflammatory M1 macrophages were repolarized to M2 phenotype by the M2 macrophage cytomembranes. As a consequence, the cytomembranes of M2 macrophage could facilitate the wound closure in mice. Furthermore, the addition of fibroblast membranes to the macrophage cytomembranes contributed to a better matrix reconstruction, neovascularization and angiogenesis. Next, we used a transforming growth factor-β (TGF-β) inhibitor to attenuate cutaneous scar formation. Therefore, our modality could promote skin wound healing and effectively suppress scar formation in the preclinical murine skin wounds. The cytomembrane biologics might provide a biocompatible and versatile tool for wound healing.

Indexed as

cytomembranefibroblastmacrophagewound healing

Identifiers

PMID36176601
PMCPMC9472019
OpenAlexW4281627412

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.