ijms-logo

Journal Browser

Journal Browser

Advanced Research on Wound Healing 2.0

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Pathology, Diagnostics, and Therapeutics".

Deadline for manuscript submissions: 20 November 2024 | Viewed by 1691

Special Issue Editor


E-Mail Website
Guest Editor
Division of Plastic Surgery, Department of Surgery, Kaohsiung Medical University Hospital, Kaohsiung 80756, Taiwan
Interests: healthy promotion; wound healing; immune tolerance
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Wound healing after damage to the skin involves a complex interplay between many cellular players of the skin, primarily keratinocytes, fibroblasts, endothelial cells of vessels and recruited immune cells, and their associated extracellular matrix. Wound healing occurs through well-orchestrated phases of hemostasis, inflammation, proliferation, and tissue remodeling.

Before migrating forward, wound-edge keratinocytes must change their cell-to-matrix adhesions. As a response to injury, endothelial progenitor cells are driven to the site of injury to initiate angiogenesis. In turn, this is arbitrated by VEGF, which triggers the activation of endothelial nitric oxide synthase (eNOS). Angiogenesis is important for providing essential components to the wound, but several cytokines (PDGF, EGF, IGF-1, and IL-8) involved in accelerating angiogenesis are downregulated in chronic wounds. Thus, the imbalance of various cells and growth factors leads to the delayed wound healing response.

With the growth of microbiome 16S ribosomal RNA sequencing opportunities, it is now possible to survey the full microbial flora of wounds, and early datasets are revealing some common genera between diabetic and venous leg ulcers. Is there a microbiota that predicts healing outcome, and can the immune response in chronic wounds be reprogrammed to be better at killing wound pathogens?

Epigenetic modifications are required for cellular differentiation and growth, but abnormal changes result in a variety of diseases. It is becoming evident that epigenetics plays an important role in wound healing, and our understanding of epigenetic control in diabetes-related complications is still limited.

Dr. Rong-Fu Chen
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. There is an Article Processing Charge (APC) for publication in this open access journal. For details about the APC please see here. Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • molecular mechanism
  • signal transduction
  • microbiota
  • DNA methylation
  • histone modifications
  • micro-RNAs
  • circRNAs
  • long noncoding RNA

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

Further information on MDPI's Special Issue polices can be found here.

Related Special Issue

Published Papers (2 papers)

Order results
Result details
Select all
Export citation of selected articles as:

Research

15 pages, 9533 KiB  
Article
Photo-Crosslinked Pro-Angiogenic Hydrogel Dressing for Wound Healing
by Wang Zhang, Shuyi Qian, Jia Chen, Tianshen Jian, Xuechun Wang, Xianmin Zhu, Yixiao Dong and Guoping Fan
Int. J. Mol. Sci. 2024, 25(18), 9948; https://doi.org/10.3390/ijms25189948 - 15 Sep 2024
Viewed by 310
Abstract
Severe burns are one of the most devastating injuries, in which sustained inflammation and ischemia often delay the healing process. Pro-angiogenic growth factors such as vascular endothelial growth factor (VEGF) have been widely studied for promoting wound healing. However, the short half-life and [...] Read more.
Severe burns are one of the most devastating injuries, in which sustained inflammation and ischemia often delay the healing process. Pro-angiogenic growth factors such as vascular endothelial growth factor (VEGF) have been widely studied for promoting wound healing. However, the short half-life and instability of VEGF limit its clinical applications. In this study, we develop a photo-crosslinked hydrogel wound dressing from methacrylate hyaluronic acid (MeHA) bonded with a pro-angiogenic prominin-1-binding peptide (PR1P). The materials were extruded in wound bed and in situ formed a wound dressing via exposure to short-time ultraviolet radiation. The study shows that the PR1P-bonded hydrogel significantly improves VEGF recruitment, tubular formation, and cell migration in vitro. Swelling, Scanning Electron Microscope, and mechanical tests indicate the peptide does not affect the overall mechanical and physical properties of the hydrogels. For in vivo studies, the PR1P-bonded hydrogel dressing enhances neovascularization and accelerates wound closure in both deep second-degree burn and full-thickness excisional wound models. The Western blot assay shows such benefits can be related to the activation of the VEGF–Akt signaling pathway. These results suggest this photo-crosslinked hydrogel dressing efficiently promotes VEGF recruitment and angiogenesis in skin regeneration, indicating its potential for clinical applications in wound healing. Full article
(This article belongs to the Special Issue Advanced Research on Wound Healing 2.0)
Show Figures

Figure 1

14 pages, 1735 KiB  
Article
Screening of the Skin-Regenerative Potential of Antimicrobial Peptides: Clavanin A, Clavanin-MO, and Mastoparan-MO
by Thuany Alencar-Silva, Rubén D Díaz-Martín, Mickelly Sousa dos Santos, Rivaldo Varejão Pasqual Saraiva, Michel Lopes Leite, Maria Tereza de Oliveira Rodrigues, Robert Pogue, Rosângela Andrade, Fabrício Falconi Costa, Nicolau Brito, Simoni Campos Dias and Juliana Lott Carvalho
Int. J. Mol. Sci. 2024, 25(13), 6851; https://doi.org/10.3390/ijms25136851 - 22 Jun 2024
Viewed by 961
Abstract
Skin wound healing is coordinated by a delicate balance between proinflammatory and anti-inflammatory responses, which can be affected by opportunistic pathogens and metabolic or vascular diseases. Several antimicrobial peptides (AMPs) possess immunomodulatory properties, suggesting their potential to support skin wound healing. Here, we [...] Read more.
Skin wound healing is coordinated by a delicate balance between proinflammatory and anti-inflammatory responses, which can be affected by opportunistic pathogens and metabolic or vascular diseases. Several antimicrobial peptides (AMPs) possess immunomodulatory properties, suggesting their potential to support skin wound healing. Here, we evaluated the proregenerative activity of three recently described AMPs (Clavanin A, Clavanin-MO, and Mastoparan-MO). Human primary dermal fibroblasts (hFibs) were used to determine peptide toxicity and their capacity to induce cell proliferation and migration. Furthermore, mRNA analysis was used to investigate the modulation of genes associated with skin regeneration. Subsequently, the regenerative potential of the peptides was further confirmed using an ex vivo organotypic model of human skin (hOSEC)-based lesion. Our results indicate that the three molecules evaluated in this study have regenerative potential at nontoxic doses (i.e., 200 μM for Clavanin-A and Clavanin-MO, and 6.25 μM for Mastoparan-MO). At these concentrations, all peptides promoted the proliferation and migration of hFibs during in vitro assays. Such processes were accompanied by gene expression signatures related to skin regenerative processes, including significantly higher KI67, HAS2 and CXCR4 mRNA levels induced by Clavanin A and Mastoparan-MO. Such findings translated into significantly accelerated wound healing promoted by both Clavanin A and Mastoparan-MO in hOSEC-based lesions. Overall, the data demonstrate the proregenerative properties of these peptides using human experimental skin models, with Mastoparan-MO and Clavanin A showing much greater potential for inducing wound healing compared to Clavanin-MO. Full article
(This article belongs to the Special Issue Advanced Research on Wound Healing 2.0)
Show Figures

Figure 1

Back to TopTop