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Comparative analysis of immune related genes between domestic pig and germ-free minipig
Recently, minipig has been considered as an animal model that is appropriate for human disease model to study toxicology, pharmacology, and xenotransplantation. Nevertheless, minipigs are bred in various environment according to their use. Here, we suggest that minipigs used for research should be b...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709342/ https://www.ncbi.nlm.nih.gov/pubmed/33292811 http://dx.doi.org/10.1186/s42826-020-00077-7 |
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author | Lee, Ju Young Kim, Sang Eun Lee, Hoon Taek Hwang, Jeong Ho |
author_facet | Lee, Ju Young Kim, Sang Eun Lee, Hoon Taek Hwang, Jeong Ho |
author_sort | Lee, Ju Young |
collection | PubMed |
description | Recently, minipig has been considered as an animal model that is appropriate for human disease model to study toxicology, pharmacology, and xenotransplantation. Nevertheless, minipigs are bred in various environment according to their use. Here, we suggest that minipigs used for research should be bred in well-controlled facility, comparing immune status of pigs raised in different breeding environment. DNA microarray was performed with ear skin and placenta of Landrace domestic pigs (DPs) and Minnesota germ-free minipigs (GPs). Their immune transcriptome was analyzed by gene ontology (GO) annotation database, based on criteria of |log(2) fold change| ≥1 with P ≤ 0.05. As a result, we found that immune related genes in the ear skin of DPs were highly activated, compared to GPs. On the other hand, no significant s were found in the placenta. Quantitative real-time PCR (qRT-PCR) was performed in five candidate immune genes. Their fold changes were consistent with the results from DNA microarray (P ≤ 0.05). In conclusion, we experimentally proved that porcine immune system was affected by different breeding environment, suggesting the importance of controlling microbes in animal room for the qualified research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42826-020-00077-7. |
format | Online Article Text |
id | pubmed-7709342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77093422020-12-03 Comparative analysis of immune related genes between domestic pig and germ-free minipig Lee, Ju Young Kim, Sang Eun Lee, Hoon Taek Hwang, Jeong Ho Lab Anim Res Research Recently, minipig has been considered as an animal model that is appropriate for human disease model to study toxicology, pharmacology, and xenotransplantation. Nevertheless, minipigs are bred in various environment according to their use. Here, we suggest that minipigs used for research should be bred in well-controlled facility, comparing immune status of pigs raised in different breeding environment. DNA microarray was performed with ear skin and placenta of Landrace domestic pigs (DPs) and Minnesota germ-free minipigs (GPs). Their immune transcriptome was analyzed by gene ontology (GO) annotation database, based on criteria of |log(2) fold change| ≥1 with P ≤ 0.05. As a result, we found that immune related genes in the ear skin of DPs were highly activated, compared to GPs. On the other hand, no significant s were found in the placenta. Quantitative real-time PCR (qRT-PCR) was performed in five candidate immune genes. Their fold changes were consistent with the results from DNA microarray (P ≤ 0.05). In conclusion, we experimentally proved that porcine immune system was affected by different breeding environment, suggesting the importance of controlling microbes in animal room for the qualified research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42826-020-00077-7. BioMed Central 2020-12-01 /pmc/articles/PMC7709342/ /pubmed/33292811 http://dx.doi.org/10.1186/s42826-020-00077-7 Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lee, Ju Young Kim, Sang Eun Lee, Hoon Taek Hwang, Jeong Ho Comparative analysis of immune related genes between domestic pig and germ-free minipig |
title | Comparative analysis of immune related genes between domestic pig and germ-free minipig |
title_full | Comparative analysis of immune related genes between domestic pig and germ-free minipig |
title_fullStr | Comparative analysis of immune related genes between domestic pig and germ-free minipig |
title_full_unstemmed | Comparative analysis of immune related genes between domestic pig and germ-free minipig |
title_short | Comparative analysis of immune related genes between domestic pig and germ-free minipig |
title_sort | comparative analysis of immune related genes between domestic pig and germ-free minipig |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7709342/ https://www.ncbi.nlm.nih.gov/pubmed/33292811 http://dx.doi.org/10.1186/s42826-020-00077-7 |
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