Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide Sublancin

Sublancin is a glycosylated antimicrobial peptide produced by Bacillus subtilis 168 with combined antibacterial and immunomodulatory activities. The purpose of this study was to evaluate the protective effects of sublancin on immunosuppression in cyclophosphamide-treated mice. In normal mice, the ph...

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Main Authors: Shuai Wang, Shuo Huang, Qianhong Ye, Xiangfang Zeng, Haitao Yu, Desheng Qi, Shiyan Qiao
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2018/4353580
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author Shuai Wang
Shuo Huang
Qianhong Ye
Xiangfang Zeng
Haitao Yu
Desheng Qi
Shiyan Qiao
author_facet Shuai Wang
Shuo Huang
Qianhong Ye
Xiangfang Zeng
Haitao Yu
Desheng Qi
Shiyan Qiao
author_sort Shuai Wang
collection DOAJ
description Sublancin is a glycosylated antimicrobial peptide produced by Bacillus subtilis 168 with combined antibacterial and immunomodulatory activities. The purpose of this study was to evaluate the protective effects of sublancin on immunosuppression in cyclophosphamide-treated mice. In normal mice, the phagocytic activity of mouse peritoneal macrophages was significantly enhanced by oral administration of sublancin (1.0 mg/kg body weight) to BALB/c mice for 7 days (P<0.01). In addition, the mRNA expression of IL-1β, IL-6, and TNF-α in peritoneal macrophages from sublancin- (1.0 mg/kg body weight) administered mice was significantly increased (P<0.05). In cyclophosphamide-treated mice, oral sublancin administration accelerated the recovery of peripheral white blood cells, red blood cells, hemoglobins, and platelets and enhanced the macrophage phagocytic activity. Furthermore, sublancin restored the mRNA levels of IL-2, IL-4, and IL-6 in the spleen. Finally, the intestinal absorption of sublancin was poor as detected in the Caco-2 transwell system. Taken together, these findings suggest that sublancin plays a crucial role in the protection against immunosuppression in cyclophosphamide-treated mice and could be a potential candidate for use in immune therapy regimens.
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issn 2314-8861
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publishDate 2018-01-01
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series Journal of Immunology Research
spelling doaj-art-d774ac60b5844174bb56afbb9da227ad2025-02-03T01:11:27ZengWileyJournal of Immunology Research2314-88612314-71562018-01-01201810.1155/2018/43535804353580Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide SublancinShuai Wang0Shuo Huang1Qianhong Ye2Xiangfang Zeng3Haitao Yu4Desheng Qi5Shiyan Qiao6State Key Laboratory of Animal Nutrition, Beijing Key Laboratory of Biofeed Additives, Ministry of Agriculture Feed Industry Centre, China Agricultural University, Beijing 100193, ChinaState Key Laboratory of Animal Nutrition, Beijing Key Laboratory of Biofeed Additives, Ministry of Agriculture Feed Industry Centre, China Agricultural University, Beijing 100193, ChinaState Key Laboratory of Animal Nutrition, Beijing Key Laboratory of Biofeed Additives, Ministry of Agriculture Feed Industry Centre, China Agricultural University, Beijing 100193, ChinaState Key Laboratory of Animal Nutrition, Beijing Key Laboratory of Biofeed Additives, Ministry of Agriculture Feed Industry Centre, China Agricultural University, Beijing 100193, ChinaState Key Laboratory of Animal Nutrition, Beijing Key Laboratory of Biofeed Additives, Ministry of Agriculture Feed Industry Centre, China Agricultural University, Beijing 100193, ChinaDepartment of Animal Nutrition and Feed Science, College of Animal Science and Technology, Huazhong Agricultural University, Wuhan, Hubei 430070, ChinaState Key Laboratory of Animal Nutrition, Beijing Key Laboratory of Biofeed Additives, Ministry of Agriculture Feed Industry Centre, China Agricultural University, Beijing 100193, ChinaSublancin is a glycosylated antimicrobial peptide produced by Bacillus subtilis 168 with combined antibacterial and immunomodulatory activities. The purpose of this study was to evaluate the protective effects of sublancin on immunosuppression in cyclophosphamide-treated mice. In normal mice, the phagocytic activity of mouse peritoneal macrophages was significantly enhanced by oral administration of sublancin (1.0 mg/kg body weight) to BALB/c mice for 7 days (P<0.01). In addition, the mRNA expression of IL-1β, IL-6, and TNF-α in peritoneal macrophages from sublancin- (1.0 mg/kg body weight) administered mice was significantly increased (P<0.05). In cyclophosphamide-treated mice, oral sublancin administration accelerated the recovery of peripheral white blood cells, red blood cells, hemoglobins, and platelets and enhanced the macrophage phagocytic activity. Furthermore, sublancin restored the mRNA levels of IL-2, IL-4, and IL-6 in the spleen. Finally, the intestinal absorption of sublancin was poor as detected in the Caco-2 transwell system. Taken together, these findings suggest that sublancin plays a crucial role in the protection against immunosuppression in cyclophosphamide-treated mice and could be a potential candidate for use in immune therapy regimens.http://dx.doi.org/10.1155/2018/4353580
spellingShingle Shuai Wang
Shuo Huang
Qianhong Ye
Xiangfang Zeng
Haitao Yu
Desheng Qi
Shiyan Qiao
Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide Sublancin
Journal of Immunology Research
title Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide Sublancin
title_full Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide Sublancin
title_fullStr Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide Sublancin
title_full_unstemmed Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide Sublancin
title_short Prevention of Cyclophosphamide-Induced Immunosuppression in Mice with the Antimicrobial Peptide Sublancin
title_sort prevention of cyclophosphamide induced immunosuppression in mice with the antimicrobial peptide sublancin
url http://dx.doi.org/10.1155/2018/4353580
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