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Survival of Skin Graft between Transgenic Cloned Dogs and Non-Transgenic Cloned Dogs
Whereas it has been assumed that genetically modified tissues or cells derived from somatic cell nuclear transfer (SCNT) should be accepted by a host of the same species, their immune compatibility has not been extensively explored. To identify acceptance of SCNT-derived cells or tissues, skin graft...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220905/ https://www.ncbi.nlm.nih.gov/pubmed/25372489 http://dx.doi.org/10.1371/journal.pone.0108330 |
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author | Kim, Geon A Oh, Hyun Ju Kim, Min Jung Jo, Young Kwang Choi, Jin Park, Jung Eun Park, Eun Jung Lim, Sang Hyun Yoon, Byung Il Kang, Sung Keun Jang, Goo Lee, Byeong Chun |
author_facet | Kim, Geon A Oh, Hyun Ju Kim, Min Jung Jo, Young Kwang Choi, Jin Park, Jung Eun Park, Eun Jung Lim, Sang Hyun Yoon, Byung Il Kang, Sung Keun Jang, Goo Lee, Byeong Chun |
author_sort | Kim, Geon A |
collection | PubMed |
description | Whereas it has been assumed that genetically modified tissues or cells derived from somatic cell nuclear transfer (SCNT) should be accepted by a host of the same species, their immune compatibility has not been extensively explored. To identify acceptance of SCNT-derived cells or tissues, skin grafts were performed between cloned dogs that were identical except for their mitochondrial DNA (mtDNA) haplotypes and foreign gene. We showed here that differences in mtDNA haplotypes and genetic modification did not elicit immune responses in these dogs: 1) skin tissues from genetically-modified cloned dogs were successfully transplanted into genetically-modified cloned dogs with different mtDNA haplotype under three successive grafts over 63 days; and 2) non-transgenic cloned tissues were accepted into transgenic cloned syngeneic recipients with different mtDNA haplotypes and vice versa under two successive grafts over 63 days. In addition, expression of the inserted gene was maintained, being functional without eliciting graft rejection. In conclusion, these results show that transplanting genetically-modified tissues into normal, syngeneic or genetically-modified recipient dogs with different mtDNA haplotypes do not elicit skin graft rejection or affect expression of the inserted gene. Therefore, therapeutically valuable tissue derived from SCNT with genetic modification might be used safely in clinical applications for patients with diseased tissues. |
format | Online Article Text |
id | pubmed-4220905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42209052014-11-12 Survival of Skin Graft between Transgenic Cloned Dogs and Non-Transgenic Cloned Dogs Kim, Geon A Oh, Hyun Ju Kim, Min Jung Jo, Young Kwang Choi, Jin Park, Jung Eun Park, Eun Jung Lim, Sang Hyun Yoon, Byung Il Kang, Sung Keun Jang, Goo Lee, Byeong Chun PLoS One Research Article Whereas it has been assumed that genetically modified tissues or cells derived from somatic cell nuclear transfer (SCNT) should be accepted by a host of the same species, their immune compatibility has not been extensively explored. To identify acceptance of SCNT-derived cells or tissues, skin grafts were performed between cloned dogs that were identical except for their mitochondrial DNA (mtDNA) haplotypes and foreign gene. We showed here that differences in mtDNA haplotypes and genetic modification did not elicit immune responses in these dogs: 1) skin tissues from genetically-modified cloned dogs were successfully transplanted into genetically-modified cloned dogs with different mtDNA haplotype under three successive grafts over 63 days; and 2) non-transgenic cloned tissues were accepted into transgenic cloned syngeneic recipients with different mtDNA haplotypes and vice versa under two successive grafts over 63 days. In addition, expression of the inserted gene was maintained, being functional without eliciting graft rejection. In conclusion, these results show that transplanting genetically-modified tissues into normal, syngeneic or genetically-modified recipient dogs with different mtDNA haplotypes do not elicit skin graft rejection or affect expression of the inserted gene. Therefore, therapeutically valuable tissue derived from SCNT with genetic modification might be used safely in clinical applications for patients with diseased tissues. Public Library of Science 2014-11-05 /pmc/articles/PMC4220905/ /pubmed/25372489 http://dx.doi.org/10.1371/journal.pone.0108330 Text en © 2014 Kim et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kim, Geon A Oh, Hyun Ju Kim, Min Jung Jo, Young Kwang Choi, Jin Park, Jung Eun Park, Eun Jung Lim, Sang Hyun Yoon, Byung Il Kang, Sung Keun Jang, Goo Lee, Byeong Chun Survival of Skin Graft between Transgenic Cloned Dogs and Non-Transgenic Cloned Dogs |
title | Survival of Skin Graft between Transgenic Cloned Dogs and Non-Transgenic Cloned Dogs |
title_full | Survival of Skin Graft between Transgenic Cloned Dogs and Non-Transgenic Cloned Dogs |
title_fullStr | Survival of Skin Graft between Transgenic Cloned Dogs and Non-Transgenic Cloned Dogs |
title_full_unstemmed | Survival of Skin Graft between Transgenic Cloned Dogs and Non-Transgenic Cloned Dogs |
title_short | Survival of Skin Graft between Transgenic Cloned Dogs and Non-Transgenic Cloned Dogs |
title_sort | survival of skin graft between transgenic cloned dogs and non-transgenic cloned dogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220905/ https://www.ncbi.nlm.nih.gov/pubmed/25372489 http://dx.doi.org/10.1371/journal.pone.0108330 |
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