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External administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice

INTRODUCTION: Artificial dermis is an effective therapeutic method for full-thickness dermal defects. However, the currently available artificial dermis made of porcine or bovine type I collagen has several limitations such as incomplete epithelialization and delayed migration of fibrogenic and angi...

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Autores principales: Sumiyoshi, Hideaki, Okamura, Yosuke, Kawaguchi, Akira T., Kubota, Tomoko, Endo, Hitoshi, Yanagawa, Takayo, Yasuda, Junpei, Matsuki, Yuki, Nakao, Sachie, Inagaki, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319749/
https://www.ncbi.nlm.nih.gov/pubmed/34377752
http://dx.doi.org/10.1016/j.reth.2021.06.008
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author Sumiyoshi, Hideaki
Okamura, Yosuke
Kawaguchi, Akira T.
Kubota, Tomoko
Endo, Hitoshi
Yanagawa, Takayo
Yasuda, Junpei
Matsuki, Yuki
Nakao, Sachie
Inagaki, Yutaka
author_facet Sumiyoshi, Hideaki
Okamura, Yosuke
Kawaguchi, Akira T.
Kubota, Tomoko
Endo, Hitoshi
Yanagawa, Takayo
Yasuda, Junpei
Matsuki, Yuki
Nakao, Sachie
Inagaki, Yutaka
author_sort Sumiyoshi, Hideaki
collection PubMed
description INTRODUCTION: Artificial dermis is an effective therapeutic method for full-thickness dermal defects. However, the currently available artificial dermis made of porcine or bovine type I collagen has several limitations such as incomplete epithelialization and delayed migration of fibrogenic and angiogenic cells into the graft. We previously developed a composite dermal graft containing a mixture of moon jellyfish collagen and porcine type I collagen, and reported its stimulatory effect on both the re-epithelialization of the epidermis and the migration of fibrogenic and angiogenic cells into the graft. In the present study, we examined whether the same effect was observed by administering jellyfish collagen solution externally onto an artificial dermal graft made of bovine type I collagen. METHODS: We used a 6 mm full-thickness wound defect model. Moon jellyfish collagen was prepared as a concentrated 0.5% solution and dripped externally onto a transplanted artificial dermal graft made of bovine type I collagen. Wound repair and long-term dermal tissue remodeling were compared between mice administered jellyfish collagen solution on the bovine collagen graft and those transplanted with a composite dermal graft containing the same amounts of jellyfish and bovine collagens. The stimulatory effect of jellyfish collagen solution was also evaluated using diabetic dB/dB mice. RESULTS: External administration of jellyfish collagen solution onto the bovine collagen graft significantly accelerated wound closure compared to control saline. It also decreased the number of inflammatory cells infiltrating the wound and suppressed absorption of the transplanted graft, as well as reduced subsequent scar formation. Furthermore, external administration of jellyfish collagen solution onto the bovine collagen graft improved the delayed wound healing in diabetic model mice, and this effect was superior to that of the currently used basic fibroblast growth factor. CONCLUSIONS: External administration of moon jellyfish collagen solution onto a bovine collagen graft significantly accelerated physiological wound healing and prevented excessive scar formation. It also improved wound closure in diabetic model mice, confirming its therapeutic application for intractable skin ulcers caused by impaired wound healing.
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spelling pubmed-83197492021-08-09 External administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice Sumiyoshi, Hideaki Okamura, Yosuke Kawaguchi, Akira T. Kubota, Tomoko Endo, Hitoshi Yanagawa, Takayo Yasuda, Junpei Matsuki, Yuki Nakao, Sachie Inagaki, Yutaka Regen Ther Original Article INTRODUCTION: Artificial dermis is an effective therapeutic method for full-thickness dermal defects. However, the currently available artificial dermis made of porcine or bovine type I collagen has several limitations such as incomplete epithelialization and delayed migration of fibrogenic and angiogenic cells into the graft. We previously developed a composite dermal graft containing a mixture of moon jellyfish collagen and porcine type I collagen, and reported its stimulatory effect on both the re-epithelialization of the epidermis and the migration of fibrogenic and angiogenic cells into the graft. In the present study, we examined whether the same effect was observed by administering jellyfish collagen solution externally onto an artificial dermal graft made of bovine type I collagen. METHODS: We used a 6 mm full-thickness wound defect model. Moon jellyfish collagen was prepared as a concentrated 0.5% solution and dripped externally onto a transplanted artificial dermal graft made of bovine type I collagen. Wound repair and long-term dermal tissue remodeling were compared between mice administered jellyfish collagen solution on the bovine collagen graft and those transplanted with a composite dermal graft containing the same amounts of jellyfish and bovine collagens. The stimulatory effect of jellyfish collagen solution was also evaluated using diabetic dB/dB mice. RESULTS: External administration of jellyfish collagen solution onto the bovine collagen graft significantly accelerated wound closure compared to control saline. It also decreased the number of inflammatory cells infiltrating the wound and suppressed absorption of the transplanted graft, as well as reduced subsequent scar formation. Furthermore, external administration of jellyfish collagen solution onto the bovine collagen graft improved the delayed wound healing in diabetic model mice, and this effect was superior to that of the currently used basic fibroblast growth factor. CONCLUSIONS: External administration of moon jellyfish collagen solution onto a bovine collagen graft significantly accelerated physiological wound healing and prevented excessive scar formation. It also improved wound closure in diabetic model mice, confirming its therapeutic application for intractable skin ulcers caused by impaired wound healing. Japanese Society for Regenerative Medicine 2021-07-19 /pmc/articles/PMC8319749/ /pubmed/34377752 http://dx.doi.org/10.1016/j.reth.2021.06.008 Text en © 2021 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Sumiyoshi, Hideaki
Okamura, Yosuke
Kawaguchi, Akira T.
Kubota, Tomoko
Endo, Hitoshi
Yanagawa, Takayo
Yasuda, Junpei
Matsuki, Yuki
Nakao, Sachie
Inagaki, Yutaka
External administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice
title External administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice
title_full External administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice
title_fullStr External administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice
title_full_unstemmed External administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice
title_short External administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice
title_sort external administration of moon jellyfish collagen solution accelerates physiological wound healing and improves delayed wound closure in diabetic model mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319749/
https://www.ncbi.nlm.nih.gov/pubmed/34377752
http://dx.doi.org/10.1016/j.reth.2021.06.008
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