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Co-expression of mFat-1 and pig IGF-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity
To develop a cost-effective molecular regulator to improve growth metabolism and immunity of animals, a recombinant plasmid co-expressing fatty acid desaturase (mFat-1) and pig insulin growth like factor 1 (IGF-1) genes was constructed by the 2 A self-cleavage technique. After entrapment within modi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719438/ https://www.ncbi.nlm.nih.gov/pubmed/29215025 http://dx.doi.org/10.1038/s41598-017-17341-x |
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author | Xiong, Qi Chen, Jianlin Li, Fei-Lin Zhao, Shiji Wan, Xiaoping Yang, Xiao Li, Jianglin Luo, Danyu Wang, Zezhou Lv, Xuebin Gao, Rong |
author_facet | Xiong, Qi Chen, Jianlin Li, Fei-Lin Zhao, Shiji Wan, Xiaoping Yang, Xiao Li, Jianglin Luo, Danyu Wang, Zezhou Lv, Xuebin Gao, Rong |
author_sort | Xiong, Qi |
collection | PubMed |
description | To develop a cost-effective molecular regulator to improve growth metabolism and immunity of animals, a recombinant plasmid co-expressing fatty acid desaturase (mFat-1) and pig insulin growth like factor 1 (IGF-1) genes was constructed by the 2 A self-cleavage technique. After entrapment within modified chitosan nanoparticles (chitosan modified with polyethyleneglycol–polyethylenimine, CPP), the recombinant plasmid was injected intramuscularly into mice. Compared with controls, co-expression of mFat-1 and IGF-1 significantly raised the level of serum IGF-1, and increased the liver and muscle docosa hexaenoic acid (DHA) content. Th and Tc cell levels were also elevated, as were expression levels of serum IL-4 and IL-6 genes. These results demonstrate that the immunity and metabolism of an animal can be effectively improved by co-expression of mFat-1 and IGF-1 genes in vivo, which may contribute to further development of novel immunomodulators with beneficial effects on growth metabolism and immunity. |
format | Online Article Text |
id | pubmed-5719438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57194382017-12-11 Co-expression of mFat-1 and pig IGF-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity Xiong, Qi Chen, Jianlin Li, Fei-Lin Zhao, Shiji Wan, Xiaoping Yang, Xiao Li, Jianglin Luo, Danyu Wang, Zezhou Lv, Xuebin Gao, Rong Sci Rep Article To develop a cost-effective molecular regulator to improve growth metabolism and immunity of animals, a recombinant plasmid co-expressing fatty acid desaturase (mFat-1) and pig insulin growth like factor 1 (IGF-1) genes was constructed by the 2 A self-cleavage technique. After entrapment within modified chitosan nanoparticles (chitosan modified with polyethyleneglycol–polyethylenimine, CPP), the recombinant plasmid was injected intramuscularly into mice. Compared with controls, co-expression of mFat-1 and IGF-1 significantly raised the level of serum IGF-1, and increased the liver and muscle docosa hexaenoic acid (DHA) content. Th and Tc cell levels were also elevated, as were expression levels of serum IL-4 and IL-6 genes. These results demonstrate that the immunity and metabolism of an animal can be effectively improved by co-expression of mFat-1 and IGF-1 genes in vivo, which may contribute to further development of novel immunomodulators with beneficial effects on growth metabolism and immunity. Nature Publishing Group UK 2017-12-07 /pmc/articles/PMC5719438/ /pubmed/29215025 http://dx.doi.org/10.1038/s41598-017-17341-x Text en © The Author(s) 2017 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 Xiong, Qi Chen, Jianlin Li, Fei-Lin Zhao, Shiji Wan, Xiaoping Yang, Xiao Li, Jianglin Luo, Danyu Wang, Zezhou Lv, Xuebin Gao, Rong Co-expression of mFat-1 and pig IGF-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity |
title | Co-expression of mFat-1 and pig IGF-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity |
title_full | Co-expression of mFat-1 and pig IGF-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity |
title_fullStr | Co-expression of mFat-1 and pig IGF-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity |
title_full_unstemmed | Co-expression of mFat-1 and pig IGF-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity |
title_short | Co-expression of mFat-1 and pig IGF-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity |
title_sort | co-expression of mfat-1 and pig igf-1 genes by recombinant plasmids in modified chitosan nanoparticles and its synergistic effect on mouse immunity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719438/ https://www.ncbi.nlm.nih.gov/pubmed/29215025 http://dx.doi.org/10.1038/s41598-017-17341-x |
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