Cargando…
In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors
The demand for equine cloning as a tool to preserve high genetic value is growing worldwide; however, nuclear transfer efficiency is still very low. To address this issue, we first evaluated the effects of time from cell fusion to activation (<1h, n = 1261; 1-2h, n = 1773; 2-3h, n = 1647) on in v...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061425/ https://www.ncbi.nlm.nih.gov/pubmed/27732616 http://dx.doi.org/10.1371/journal.pone.0164049 |
_version_ | 1782459604331921408 |
---|---|
author | Olivera, Ramiro Moro, Lucia Natalia Jordan, Roberto Luzzani, Carlos Miriuka, Santiago Radrizzani, Martin Donadeu, F. Xavier Vichera, Gabriel |
author_facet | Olivera, Ramiro Moro, Lucia Natalia Jordan, Roberto Luzzani, Carlos Miriuka, Santiago Radrizzani, Martin Donadeu, F. Xavier Vichera, Gabriel |
author_sort | Olivera, Ramiro |
collection | PubMed |
description | The demand for equine cloning as a tool to preserve high genetic value is growing worldwide; however, nuclear transfer efficiency is still very low. To address this issue, we first evaluated the effects of time from cell fusion to activation (<1h, n = 1261; 1-2h, n = 1773; 2-3h, n = 1647) on in vitro and in vivo development of equine embryos generated by cloning. Then, we evaluated the effects of using different nuclear donor cell types in two successive experiments: I) induced pluripotent stem cells (iPSCs) vs. adult fibroblasts (AF) fused to ooplasts injected with the pluripotency-inducing genes OCT4, SOX2, MYC and KLF4, vs. AF alone as controls; II) umbilical cord-derived mesenchymal stromal cells (UC-MSCs) vs. fetal fibroblasts derived from an unborn cloned foetus (FF) vs. AF from the original individual. In the first experiment, both blastocyst production and pregnancy rates were higher in the 2-3h group (11.5% and 9.5%, respectively), respect to <1h (5.2% and 2%, respectively) and 1-2h (5.6% and 4.7%, respectively) groups (P<0.05). However, percentages of born foals/pregnancies were similar when intervals of 2-3h (35.2%) or 1-2h (35.7%) were used. In contrast to AF, the iPSCs did not generate any blastocyst-stage embryos. Moreover, injection of oocytes with the pluripotency-inducing genes did not improve blastocyst production nor pregnancy rates respect to AF controls. Finally, higher blastocyst production was obtained using UC-MSC (15.6%) than using FF (8.9%) or AF (9.3%), (P<0.05). Despite pregnancy rates were similar for these 3 groups (17.6%, 18.2% and 22%, respectively), viable foals (two) were obtained only by using FF. In summary, optimum blastocyst production rates can be obtained using a 2-3h interval between cell fusion and activation as well as using UC-MSCs as nuclear donors. Moreover, FF line can improve the efficiency of an inefficient AF line. Overall, 24 healthy foals were obtained from a total of 29 born foals. |
format | Online Article Text |
id | pubmed-5061425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-50614252016-10-27 In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors Olivera, Ramiro Moro, Lucia Natalia Jordan, Roberto Luzzani, Carlos Miriuka, Santiago Radrizzani, Martin Donadeu, F. Xavier Vichera, Gabriel PLoS One Research Article The demand for equine cloning as a tool to preserve high genetic value is growing worldwide; however, nuclear transfer efficiency is still very low. To address this issue, we first evaluated the effects of time from cell fusion to activation (<1h, n = 1261; 1-2h, n = 1773; 2-3h, n = 1647) on in vitro and in vivo development of equine embryos generated by cloning. Then, we evaluated the effects of using different nuclear donor cell types in two successive experiments: I) induced pluripotent stem cells (iPSCs) vs. adult fibroblasts (AF) fused to ooplasts injected with the pluripotency-inducing genes OCT4, SOX2, MYC and KLF4, vs. AF alone as controls; II) umbilical cord-derived mesenchymal stromal cells (UC-MSCs) vs. fetal fibroblasts derived from an unborn cloned foetus (FF) vs. AF from the original individual. In the first experiment, both blastocyst production and pregnancy rates were higher in the 2-3h group (11.5% and 9.5%, respectively), respect to <1h (5.2% and 2%, respectively) and 1-2h (5.6% and 4.7%, respectively) groups (P<0.05). However, percentages of born foals/pregnancies were similar when intervals of 2-3h (35.2%) or 1-2h (35.7%) were used. In contrast to AF, the iPSCs did not generate any blastocyst-stage embryos. Moreover, injection of oocytes with the pluripotency-inducing genes did not improve blastocyst production nor pregnancy rates respect to AF controls. Finally, higher blastocyst production was obtained using UC-MSC (15.6%) than using FF (8.9%) or AF (9.3%), (P<0.05). Despite pregnancy rates were similar for these 3 groups (17.6%, 18.2% and 22%, respectively), viable foals (two) were obtained only by using FF. In summary, optimum blastocyst production rates can be obtained using a 2-3h interval between cell fusion and activation as well as using UC-MSCs as nuclear donors. Moreover, FF line can improve the efficiency of an inefficient AF line. Overall, 24 healthy foals were obtained from a total of 29 born foals. Public Library of Science 2016-10-12 /pmc/articles/PMC5061425/ /pubmed/27732616 http://dx.doi.org/10.1371/journal.pone.0164049 Text en © 2016 Olivera 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Olivera, Ramiro Moro, Lucia Natalia Jordan, Roberto Luzzani, Carlos Miriuka, Santiago Radrizzani, Martin Donadeu, F. Xavier Vichera, Gabriel In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors |
title | In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors |
title_full | In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors |
title_fullStr | In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors |
title_full_unstemmed | In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors |
title_short | In Vitro and In Vivo Development of Horse Cloned Embryos Generated with iPSCs, Mesenchymal Stromal Cells and Fetal or Adult Fibroblasts as Nuclear Donors |
title_sort | in vitro and in vivo development of horse cloned embryos generated with ipscs, mesenchymal stromal cells and fetal or adult fibroblasts as nuclear donors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5061425/ https://www.ncbi.nlm.nih.gov/pubmed/27732616 http://dx.doi.org/10.1371/journal.pone.0164049 |
work_keys_str_mv | AT oliveraramiro invitroandinvivodevelopmentofhorseclonedembryosgeneratedwithipscsmesenchymalstromalcellsandfetaloradultfibroblastsasnucleardonors AT morolucianatalia invitroandinvivodevelopmentofhorseclonedembryosgeneratedwithipscsmesenchymalstromalcellsandfetaloradultfibroblastsasnucleardonors AT jordanroberto invitroandinvivodevelopmentofhorseclonedembryosgeneratedwithipscsmesenchymalstromalcellsandfetaloradultfibroblastsasnucleardonors AT luzzanicarlos invitroandinvivodevelopmentofhorseclonedembryosgeneratedwithipscsmesenchymalstromalcellsandfetaloradultfibroblastsasnucleardonors AT miriukasantiago invitroandinvivodevelopmentofhorseclonedembryosgeneratedwithipscsmesenchymalstromalcellsandfetaloradultfibroblastsasnucleardonors AT radrizzanimartin invitroandinvivodevelopmentofhorseclonedembryosgeneratedwithipscsmesenchymalstromalcellsandfetaloradultfibroblastsasnucleardonors AT donadeufxavier invitroandinvivodevelopmentofhorseclonedembryosgeneratedwithipscsmesenchymalstromalcellsandfetaloradultfibroblastsasnucleardonors AT vicheragabriel invitroandinvivodevelopmentofhorseclonedembryosgeneratedwithipscsmesenchymalstromalcellsandfetaloradultfibroblastsasnucleardonors |