Salmon cartilage proteoglycan promotes the healing process of Staphylococcus aureus-infected wound

Wound healing is the critical event for maintaining skin function and barrier. Inflammatory state in which a variety of cells are activated and accumulated is important for wound healing. Bacterial infection in cutaneous wound is a common problem and causes delay of wound healing. Our previous study...

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Main Authors: Shouhei Hirose, Kouji Narita, Krisana Asano, Akio Nakane
Format: Article
Language:English
Published: Elsevier 2018-03-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844017330426
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spelling doaj-80e2c75bfc2c46269c90b67c95bee9fd2020-11-25T02:14:04ZengElsevierHeliyon2405-84402018-03-0143e00587Salmon cartilage proteoglycan promotes the healing process of Staphylococcus aureus-infected woundShouhei Hirose0Kouji Narita1Krisana Asano2Akio Nakane3Department of Microbiology and Immunology, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori 036-8562, Japan; Department of Biopolymer and Health Science, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori 036-8562, JapanDepartment of Microbiology and Immunology, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori 036-8562, Japan; Institute for Animal Experimentation, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori 036-8562, JapanDepartment of Microbiology and Immunology, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori 036-8562, Japan; Department of Biopolymer and Health Science, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori 036-8562, Japan; Corresponding authors.Department of Microbiology and Immunology, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori 036-8562, Japan; Department of Biopolymer and Health Science, Hirosaki University Graduate School of Medicine, 5 Zaifu-cho, Hirosaki, Aomori 036-8562, Japan; Corresponding authors.Wound healing is the critical event for maintaining skin function and barrier. Inflammatory state in which a variety of cells are activated and accumulated is important for wound healing. Bacterial infection in cutaneous wound is a common problem and causes delay of wound healing. Our previous study demonstrated that the salmon nasal cartilage proteoglycan (PG) has an immunomodulatory effect in various mouse models of inflammatory disease. In this study, we investigated the effect of PG on healing process of Staphylococcus aureus-infected wound. PG accelerated wound closure in the initial phase of both infected and non-infected wound healing. In addition, the bacterial number in wounds of the PG-treated mice was significantly lower than that in the vehicle group. Neutrophil and macrophage infiltration was intensively observed in the PG-treated mice on day 2 after S. aureus inoculation, whereas neutrophil and macrophage influx was highly detected on day 6 in the vehicle control. Moreover, the production of TGF-β and IL-6 in the wound tissue was significantly promoted compared to the vehicle control on day 1. In contrast, the production of IL-1β and TNF-α in PG-treated mice was significantly decreased compared to the vehicle control on day 5. These data suggested that PG modulates the inflammatory state in infected wounds leading to promote wound healing.http://www.sciencedirect.com/science/article/pii/S2405844017330426MicrobiologyPharmaceutical chemistry
collection DOAJ
language English
format Article
sources DOAJ
author Shouhei Hirose
Kouji Narita
Krisana Asano
Akio Nakane
spellingShingle Shouhei Hirose
Kouji Narita
Krisana Asano
Akio Nakane
Salmon cartilage proteoglycan promotes the healing process of Staphylococcus aureus-infected wound
Heliyon
Microbiology
Pharmaceutical chemistry
author_facet Shouhei Hirose
Kouji Narita
Krisana Asano
Akio Nakane
author_sort Shouhei Hirose
title Salmon cartilage proteoglycan promotes the healing process of Staphylococcus aureus-infected wound
title_short Salmon cartilage proteoglycan promotes the healing process of Staphylococcus aureus-infected wound
title_full Salmon cartilage proteoglycan promotes the healing process of Staphylococcus aureus-infected wound
title_fullStr Salmon cartilage proteoglycan promotes the healing process of Staphylococcus aureus-infected wound
title_full_unstemmed Salmon cartilage proteoglycan promotes the healing process of Staphylococcus aureus-infected wound
title_sort salmon cartilage proteoglycan promotes the healing process of staphylococcus aureus-infected wound
publisher Elsevier
series Heliyon
issn 2405-8440
publishDate 2018-03-01
description Wound healing is the critical event for maintaining skin function and barrier. Inflammatory state in which a variety of cells are activated and accumulated is important for wound healing. Bacterial infection in cutaneous wound is a common problem and causes delay of wound healing. Our previous study demonstrated that the salmon nasal cartilage proteoglycan (PG) has an immunomodulatory effect in various mouse models of inflammatory disease. In this study, we investigated the effect of PG on healing process of Staphylococcus aureus-infected wound. PG accelerated wound closure in the initial phase of both infected and non-infected wound healing. In addition, the bacterial number in wounds of the PG-treated mice was significantly lower than that in the vehicle group. Neutrophil and macrophage infiltration was intensively observed in the PG-treated mice on day 2 after S. aureus inoculation, whereas neutrophil and macrophage influx was highly detected on day 6 in the vehicle control. Moreover, the production of TGF-β and IL-6 in the wound tissue was significantly promoted compared to the vehicle control on day 1. In contrast, the production of IL-1β and TNF-α in PG-treated mice was significantly decreased compared to the vehicle control on day 5. These data suggested that PG modulates the inflammatory state in infected wounds leading to promote wound healing.
topic Microbiology
Pharmaceutical chemistry
url http://www.sciencedirect.com/science/article/pii/S2405844017330426
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