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Marine microalgae bioengineered Schizochytrium sp. meal hydrolysates inhibits acute inflammation
Bioengineered marine microalgae Schizochytrium sp. is currently used to produce docosahexaenoic acid (DHA). However, following DHA extraction, the remaining protein-rich materials are not well utilized. In this study, we report that marine microalgae bioengineered Schizochytrium sp. hydrolysate (MES...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026148/ https://www.ncbi.nlm.nih.gov/pubmed/29959357 http://dx.doi.org/10.1038/s41598-018-28064-y |
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author | Wang, Xiaoli Wang, Heng Pierre, Joseph F. Wang, Sheng Huang, Huifang Zhang, Jun Liang, Shuangzhen Zeng, Qingzhu Zhang, Chenqing Huang, Meijuan Ruan, Chengxu Lin, Juan Li, Hao |
author_facet | Wang, Xiaoli Wang, Heng Pierre, Joseph F. Wang, Sheng Huang, Huifang Zhang, Jun Liang, Shuangzhen Zeng, Qingzhu Zhang, Chenqing Huang, Meijuan Ruan, Chengxu Lin, Juan Li, Hao |
author_sort | Wang, Xiaoli |
collection | PubMed |
description | Bioengineered marine microalgae Schizochytrium sp. is currently used to produce docosahexaenoic acid (DHA). However, following DHA extraction, the remaining protein-rich materials are not well utilized. In this study, we report that marine microalgae bioengineered Schizochytrium sp. hydrolysate (MESH), which exhibits a unique peptide profile as identified by Ultra Performance Liquid Chromatography coupled with Q-TOF mass spectrometry(UPLC/Q-TOF-MS), ameliorated bowel inflammation in mice. In a mouse model of experimentalcolitis induced by dextran sulfate sodium, compared with the control mice, the mice treated with MESH were highly resistant to colitis, as demonstrated by marked reductions in body weight loss, clinical colitis scores, colonic histological damage, and colonic inflammation. Mechanistically, MESH attenuated the induction of pro-inflammatory cytokines and increased the induction of anti-inflammatory cytokines. MESH also promoted the proliferation of colonic crypt stem cells and progenitor cells required for crypt repair. Collectively, these results reveal a previously unrecognized role of MESH as a potential anti-inflammatory treatment for colitis. |
format | Online Article Text |
id | pubmed-6026148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60261482018-07-09 Marine microalgae bioengineered Schizochytrium sp. meal hydrolysates inhibits acute inflammation Wang, Xiaoli Wang, Heng Pierre, Joseph F. Wang, Sheng Huang, Huifang Zhang, Jun Liang, Shuangzhen Zeng, Qingzhu Zhang, Chenqing Huang, Meijuan Ruan, Chengxu Lin, Juan Li, Hao Sci Rep Article Bioengineered marine microalgae Schizochytrium sp. is currently used to produce docosahexaenoic acid (DHA). However, following DHA extraction, the remaining protein-rich materials are not well utilized. In this study, we report that marine microalgae bioengineered Schizochytrium sp. hydrolysate (MESH), which exhibits a unique peptide profile as identified by Ultra Performance Liquid Chromatography coupled with Q-TOF mass spectrometry(UPLC/Q-TOF-MS), ameliorated bowel inflammation in mice. In a mouse model of experimentalcolitis induced by dextran sulfate sodium, compared with the control mice, the mice treated with MESH were highly resistant to colitis, as demonstrated by marked reductions in body weight loss, clinical colitis scores, colonic histological damage, and colonic inflammation. Mechanistically, MESH attenuated the induction of pro-inflammatory cytokines and increased the induction of anti-inflammatory cytokines. MESH also promoted the proliferation of colonic crypt stem cells and progenitor cells required for crypt repair. Collectively, these results reveal a previously unrecognized role of MESH as a potential anti-inflammatory treatment for colitis. Nature Publishing Group UK 2018-06-29 /pmc/articles/PMC6026148/ /pubmed/29959357 http://dx.doi.org/10.1038/s41598-018-28064-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Xiaoli Wang, Heng Pierre, Joseph F. Wang, Sheng Huang, Huifang Zhang, Jun Liang, Shuangzhen Zeng, Qingzhu Zhang, Chenqing Huang, Meijuan Ruan, Chengxu Lin, Juan Li, Hao Marine microalgae bioengineered Schizochytrium sp. meal hydrolysates inhibits acute inflammation |
title | Marine microalgae bioengineered Schizochytrium sp. meal hydrolysates inhibits acute inflammation |
title_full | Marine microalgae bioengineered Schizochytrium sp. meal hydrolysates inhibits acute inflammation |
title_fullStr | Marine microalgae bioengineered Schizochytrium sp. meal hydrolysates inhibits acute inflammation |
title_full_unstemmed | Marine microalgae bioengineered Schizochytrium sp. meal hydrolysates inhibits acute inflammation |
title_short | Marine microalgae bioengineered Schizochytrium sp. meal hydrolysates inhibits acute inflammation |
title_sort | marine microalgae bioengineered schizochytrium sp. meal hydrolysates inhibits acute inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026148/ https://www.ncbi.nlm.nih.gov/pubmed/29959357 http://dx.doi.org/10.1038/s41598-018-28064-y |
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