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Research progress and insights on the role of ferroptosis in wound healing

Ferroptosis is a newly discovered cell death type which is different from apoptosis, autophagy, pyroptosis as well as necrosis in the following aspects: morphology, biochemistry, gene and regulatory mechanisms. Ferroptosis is regulated by multiples of mechanisms such as system Xc(−) mechanism, gluta...

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Detalles Bibliográficos
Autores principales: Bi, Minglei, Li, Danyi, Zhang, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333008/
https://www.ncbi.nlm.nih.gov/pubmed/36788729
http://dx.doi.org/10.1111/iwj.14102
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author Bi, Minglei
Li, Danyi
Zhang, Jin
author_facet Bi, Minglei
Li, Danyi
Zhang, Jin
author_sort Bi, Minglei
collection PubMed
description Ferroptosis is a newly discovered cell death type which is different from apoptosis, autophagy, pyroptosis as well as necrosis in the following aspects: morphology, biochemistry, gene and regulatory mechanisms. Ferroptosis is regulated by multiples of mechanisms such as system Xc(−) mechanism, glutathione peroxidase 4 (GPX4) mechanism, iron metabolism and lipid metabolism. Currently, ferroptosis has been revealed to be significant in wound healing such as diabetic wound, irradiated wound and ultraviolet (UV)‐driven wound. Hence, how to intervene in the pathogenesis as well as the development of wounds and promote the wound healing by the regulation of ferroptosis have become a research hotspot. This review systematically summarises the latest scientific advances of ferroptosis and wound healing fields, with hoping to propose a new insight and advance in the wound treatment.
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spelling pubmed-103330082023-07-12 Research progress and insights on the role of ferroptosis in wound healing Bi, Minglei Li, Danyi Zhang, Jin Int Wound J Review Articles Ferroptosis is a newly discovered cell death type which is different from apoptosis, autophagy, pyroptosis as well as necrosis in the following aspects: morphology, biochemistry, gene and regulatory mechanisms. Ferroptosis is regulated by multiples of mechanisms such as system Xc(−) mechanism, glutathione peroxidase 4 (GPX4) mechanism, iron metabolism and lipid metabolism. Currently, ferroptosis has been revealed to be significant in wound healing such as diabetic wound, irradiated wound and ultraviolet (UV)‐driven wound. Hence, how to intervene in the pathogenesis as well as the development of wounds and promote the wound healing by the regulation of ferroptosis have become a research hotspot. This review systematically summarises the latest scientific advances of ferroptosis and wound healing fields, with hoping to propose a new insight and advance in the wound treatment. Blackwell Publishing Ltd 2023-02-14 /pmc/articles/PMC10333008/ /pubmed/36788729 http://dx.doi.org/10.1111/iwj.14102 Text en © 2023 The Authors. International Wound Journal published by Medicalhelplines.com Inc and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review Articles
Bi, Minglei
Li, Danyi
Zhang, Jin
Research progress and insights on the role of ferroptosis in wound healing
title Research progress and insights on the role of ferroptosis in wound healing
title_full Research progress and insights on the role of ferroptosis in wound healing
title_fullStr Research progress and insights on the role of ferroptosis in wound healing
title_full_unstemmed Research progress and insights on the role of ferroptosis in wound healing
title_short Research progress and insights on the role of ferroptosis in wound healing
title_sort research progress and insights on the role of ferroptosis in wound healing
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333008/
https://www.ncbi.nlm.nih.gov/pubmed/36788729
http://dx.doi.org/10.1111/iwj.14102
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