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Primed Pluripotent Cell Lines Derived from Various Embryonic Origins and Somatic Cells in Pig

Since pluripotent embryonic stem cell (ESC) lines were first derived from the mouse, tremendous efforts have been made to establish ESC lines in several domestic species including the pig; however, authentic porcine ESCs have not yet been established. It has proven difficult to maintain an ESC-like...

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Autores principales: Park, Jin-Kyu, Kim, Hye-Sun, Uh, Kyung-Jun, Choi, Kwang-Hwan, Kim, Hyeong-Min, Lee, Taeheon, Yang, Byung-Chul, Kim, Hyun-Jong, Ka, Hak-Hyun, Kim, Heebal, Lee, Chang-Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543426/
https://www.ncbi.nlm.nih.gov/pubmed/23326334
http://dx.doi.org/10.1371/journal.pone.0052481
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author Park, Jin-Kyu
Kim, Hye-Sun
Uh, Kyung-Jun
Choi, Kwang-Hwan
Kim, Hyeong-Min
Lee, Taeheon
Yang, Byung-Chul
Kim, Hyun-Jong
Ka, Hak-Hyun
Kim, Heebal
Lee, Chang-Kyu
author_facet Park, Jin-Kyu
Kim, Hye-Sun
Uh, Kyung-Jun
Choi, Kwang-Hwan
Kim, Hyeong-Min
Lee, Taeheon
Yang, Byung-Chul
Kim, Hyun-Jong
Ka, Hak-Hyun
Kim, Heebal
Lee, Chang-Kyu
author_sort Park, Jin-Kyu
collection PubMed
description Since pluripotent embryonic stem cell (ESC) lines were first derived from the mouse, tremendous efforts have been made to establish ESC lines in several domestic species including the pig; however, authentic porcine ESCs have not yet been established. It has proven difficult to maintain an ESC-like state in pluripotent porcine cell lines due to the frequent occurrence of spontaneous differentiation into an epiblast stem cell (EpiSC)-like state during culture. We have been able to derive EpiSC-like porcine ESC (pESC) lines from blastocyst stage porcine embryos of various origins, including in vitro fertilized (IVF), in vivo derived, IVF aggregated, and parthenogenetic embryos. In addition, we have generated induced pluripotent stem cells (piPSCs) via plasmid transfection of reprogramming factors (Oct4, Sox2, Klf4, and c-Myc) into porcine fibroblast cells. In this study, we analyzed characteristics such as marker expression, pluripotency and the X chromosome inactivation status in female of our EpiSC-like pESC lines along with our piPSC line. Our results show that these cell lines demonstrate the expression of genes associated with the Activin/Nodal and FGF2 pathways along with the expression of pluripotent markers Oct4, Sox2, Nanog, SSEA4, TRA 1–60 and TRA 1–81. Furthermore all of these cell lines showed in vitro differentiation potential, the X chromosome inactivation in female and a normal karyotype. Here we suggest that the porcine species undergoes reprogramming into a primed state during the establishment of pluripotent stem cell lines.
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spelling pubmed-35434262013-01-16 Primed Pluripotent Cell Lines Derived from Various Embryonic Origins and Somatic Cells in Pig Park, Jin-Kyu Kim, Hye-Sun Uh, Kyung-Jun Choi, Kwang-Hwan Kim, Hyeong-Min Lee, Taeheon Yang, Byung-Chul Kim, Hyun-Jong Ka, Hak-Hyun Kim, Heebal Lee, Chang-Kyu PLoS One Research Article Since pluripotent embryonic stem cell (ESC) lines were first derived from the mouse, tremendous efforts have been made to establish ESC lines in several domestic species including the pig; however, authentic porcine ESCs have not yet been established. It has proven difficult to maintain an ESC-like state in pluripotent porcine cell lines due to the frequent occurrence of spontaneous differentiation into an epiblast stem cell (EpiSC)-like state during culture. We have been able to derive EpiSC-like porcine ESC (pESC) lines from blastocyst stage porcine embryos of various origins, including in vitro fertilized (IVF), in vivo derived, IVF aggregated, and parthenogenetic embryos. In addition, we have generated induced pluripotent stem cells (piPSCs) via plasmid transfection of reprogramming factors (Oct4, Sox2, Klf4, and c-Myc) into porcine fibroblast cells. In this study, we analyzed characteristics such as marker expression, pluripotency and the X chromosome inactivation status in female of our EpiSC-like pESC lines along with our piPSC line. Our results show that these cell lines demonstrate the expression of genes associated with the Activin/Nodal and FGF2 pathways along with the expression of pluripotent markers Oct4, Sox2, Nanog, SSEA4, TRA 1–60 and TRA 1–81. Furthermore all of these cell lines showed in vitro differentiation potential, the X chromosome inactivation in female and a normal karyotype. Here we suggest that the porcine species undergoes reprogramming into a primed state during the establishment of pluripotent stem cell lines. Public Library of Science 2013-01-11 /pmc/articles/PMC3543426/ /pubmed/23326334 http://dx.doi.org/10.1371/journal.pone.0052481 Text en © 2013 Park 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
Park, Jin-Kyu
Kim, Hye-Sun
Uh, Kyung-Jun
Choi, Kwang-Hwan
Kim, Hyeong-Min
Lee, Taeheon
Yang, Byung-Chul
Kim, Hyun-Jong
Ka, Hak-Hyun
Kim, Heebal
Lee, Chang-Kyu
Primed Pluripotent Cell Lines Derived from Various Embryonic Origins and Somatic Cells in Pig
title Primed Pluripotent Cell Lines Derived from Various Embryonic Origins and Somatic Cells in Pig
title_full Primed Pluripotent Cell Lines Derived from Various Embryonic Origins and Somatic Cells in Pig
title_fullStr Primed Pluripotent Cell Lines Derived from Various Embryonic Origins and Somatic Cells in Pig
title_full_unstemmed Primed Pluripotent Cell Lines Derived from Various Embryonic Origins and Somatic Cells in Pig
title_short Primed Pluripotent Cell Lines Derived from Various Embryonic Origins and Somatic Cells in Pig
title_sort primed pluripotent cell lines derived from various embryonic origins and somatic cells in pig
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3543426/
https://www.ncbi.nlm.nih.gov/pubmed/23326334
http://dx.doi.org/10.1371/journal.pone.0052481
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