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Non-denatured yak type I collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen

Sunburn is one of the most common skin lesions caused by excessive UV exposure, and its incidence is highly correlated with the risks of skin cancer. A variety of drugs including corticosteroids and NSAIDs have been developed to treat acute sunburn, however, they have raised severe concerns such as...

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Autores principales: Fu, Caihong, Shi, Shuangni, Tian, Jing, Gu, Hong, Yao, Linyan, Xiao, Jianxi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791591/
https://www.ncbi.nlm.nih.gov/pubmed/36578365
http://dx.doi.org/10.1016/j.btre.2022.e00778
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author Fu, Caihong
Shi, Shuangni
Tian, Jing
Gu, Hong
Yao, Linyan
Xiao, Jianxi
author_facet Fu, Caihong
Shi, Shuangni
Tian, Jing
Gu, Hong
Yao, Linyan
Xiao, Jianxi
author_sort Fu, Caihong
collection PubMed
description Sunburn is one of the most common skin lesions caused by excessive UV exposure, and its incidence is highly correlated with the risks of skin cancer. A variety of drugs including corticosteroids and NSAIDs have been developed to treat acute sunburn, however, they have raised severe concerns such as poor healing efficacy and long recovery time. We have for the first time extracted non-denatured type I collagen from yak hide, which displays a canonical triple helical structure with melting temperature of 42.7 °C. The highly pure yak collagen type I (YCI) self-assembles to form well-ordered nanofibers with periodic d-bands. YCI is highly biocompatible, and it significantly promotes the proliferation and adhesion of HFF-1 cells. The sunburn healing effects of YCI has been investigated using acute skin injury mouse model. Histological analysis shows that 4 days’ treatment of YCI has resulted in the recovery of sunburned mice skin to a healthy state, indicated by pronounced acceleration of epithelization and collagen deposition. The collagen volume fraction as well as the hydroxyproline (Hyp) content of YCI-treated sunburned skin have been found to be greatly increased, confirming the enhanced regeneration of collagen. YCI creams and dressings have also shown superior healing capacity of sunburn by remarkably shortening the recovery time. Notably, the denatured collagen-targeted staining results indicated a large quantity of denatured collagen in sunburned mice, which became substantially reduced after the YCI treatment. FITC-labeled YCI has been further found to penetrate into the dermis of sunburned mice. The highly biocompatible and bioactive non-denatured YCI provides an improved treatment of sunburn, indicating very promising applications of YCI in cosmetics and dermatology.
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spelling pubmed-97915912022-12-27 Non-denatured yak type I collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen Fu, Caihong Shi, Shuangni Tian, Jing Gu, Hong Yao, Linyan Xiao, Jianxi Biotechnol Rep (Amst) Research Article Sunburn is one of the most common skin lesions caused by excessive UV exposure, and its incidence is highly correlated with the risks of skin cancer. A variety of drugs including corticosteroids and NSAIDs have been developed to treat acute sunburn, however, they have raised severe concerns such as poor healing efficacy and long recovery time. We have for the first time extracted non-denatured type I collagen from yak hide, which displays a canonical triple helical structure with melting temperature of 42.7 °C. The highly pure yak collagen type I (YCI) self-assembles to form well-ordered nanofibers with periodic d-bands. YCI is highly biocompatible, and it significantly promotes the proliferation and adhesion of HFF-1 cells. The sunburn healing effects of YCI has been investigated using acute skin injury mouse model. Histological analysis shows that 4 days’ treatment of YCI has resulted in the recovery of sunburned mice skin to a healthy state, indicated by pronounced acceleration of epithelization and collagen deposition. The collagen volume fraction as well as the hydroxyproline (Hyp) content of YCI-treated sunburned skin have been found to be greatly increased, confirming the enhanced regeneration of collagen. YCI creams and dressings have also shown superior healing capacity of sunburn by remarkably shortening the recovery time. Notably, the denatured collagen-targeted staining results indicated a large quantity of denatured collagen in sunburned mice, which became substantially reduced after the YCI treatment. FITC-labeled YCI has been further found to penetrate into the dermis of sunburned mice. The highly biocompatible and bioactive non-denatured YCI provides an improved treatment of sunburn, indicating very promising applications of YCI in cosmetics and dermatology. Elsevier 2022-12-17 /pmc/articles/PMC9791591/ /pubmed/36578365 http://dx.doi.org/10.1016/j.btre.2022.e00778 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Fu, Caihong
Shi, Shuangni
Tian, Jing
Gu, Hong
Yao, Linyan
Xiao, Jianxi
Non-denatured yak type I collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen
title Non-denatured yak type I collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen
title_full Non-denatured yak type I collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen
title_fullStr Non-denatured yak type I collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen
title_full_unstemmed Non-denatured yak type I collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen
title_short Non-denatured yak type I collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen
title_sort non-denatured yak type i collagen accelerates sunburned skin healing by stimulating and replenishing dermal collagen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791591/
https://www.ncbi.nlm.nih.gov/pubmed/36578365
http://dx.doi.org/10.1016/j.btre.2022.e00778
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