OxInflammation Affects Transdifferentiation to Myofibroblasts, Prolonging Wound Healing in Diabetes: A Systematic Review

• Published in: International journal of molecular sciences Vol. 25; no. 16; p. 8992
• Main Authors: Silveira, Leonardo L., Sarandy, Mariáurea M., Novaes, Rômulo D., Morais-Santos, Mônica, Gonçalves, Reggiani V.
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 19.08.2024; MDPI
• Subjects: Angiogenesis; Animals; Cell Transdifferentiation; Diabetes; Diabetes Mellitus - metabolism; Diabetes Mellitus - pathology; Extracellular matrix; Fibroblasts; Growth factors; Inflammation; Inflammation - metabolism; Inflammation - pathology; Kinases; Laboratory animals; Medical Subject Headings-MeSH; Mice; Myofibroblasts - metabolism; Myofibroblasts - pathology; Oxidative stress; Product development; Review; Skin; Smooth muscle; Systematic review; Transforming Growth Factor beta - metabolism; Tumor necrosis factor-TNF; Ulcers; Wound Healing; TGF-beta; wound healing; OxInflammation process; inflammasome; NLRP3; cytokines; diabetes mellitus; myofibroblasts
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25168992

Skin wounds, primarily in association with type I diabetes mellitus, are a public health problem generating significant health impacts. Therefore, identifying the main pathways/mechanisms involved in differentiating fibroblasts into myofibroblasts is fundamental to guide research into effective treatments. Adopting the PRISMA guidelines, this study aimed to verify the main pathways/mechanisms using diabetic murine models and analyze the advances and limitations of this area. The Medline (PubMed), Scopus, and Web of Science platforms were used for the search. The studies included were limited to those that used diabetic murine models with excisional wounds. Bias analysis and methodological quality assessments were undertaken using the SYRCLE bias risk tool. Eighteen studies were selected. The systematic review results confirm that diabetes impairs the transformation of fibroblasts into myofibroblasts by affecting the expression of several growth factors, most notably transforming growth factor beta (TGF-beta) and NLRP3. Diabetes also compromises pathways such as the SMAD, c-Jun N-terminal kinase, protein kinase C, and nuclear factor kappa beta activating caspase pathways, leading to cell death. Furthermore, diabetes renders the wound environment highly pro-oxidant and inflammatory, which is known as OxInflammation. As a consequence of this OxInflammation, delays in the collagenization process occur. The protocol details for this systematic review were registered with PROSPERO: CRD42021267776.