Cargando…
Production of transgenic cattle by somatic cell nuclear transfer (SCNT) with the human granulocyte colony-stimulation factor (hG-CSF)
The hG-CSF (human Granulocyte Colony-Stimulating Factor) is a growth and stimulation factor capable of inducing the proliferation of bone marrow cells, several types of leukocytes, among other hematopoietic tissue cells. hG-CSF is used in used to treat anomalies that reder a small number of circulat...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Animal Science and Technology
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582935/ https://www.ncbi.nlm.nih.gov/pubmed/31333863 http://dx.doi.org/10.5187/jast.2019.61.2.61 |
_version_ | 1783428430522482688 |
---|---|
author | Carvalho, Bruno P. Cunha, Andrielle T. M. Silva, Bianca D. M. Sousa, Regivaldo V. Leme, Ligiane O. Dode, Margot A. N. Melo, Eduardo O. |
author_facet | Carvalho, Bruno P. Cunha, Andrielle T. M. Silva, Bianca D. M. Sousa, Regivaldo V. Leme, Ligiane O. Dode, Margot A. N. Melo, Eduardo O. |
author_sort | Carvalho, Bruno P. |
collection | PubMed |
description | The hG-CSF (human Granulocyte Colony-Stimulating Factor) is a growth and stimulation factor capable of inducing the proliferation of bone marrow cells, several types of leukocytes, among other hematopoietic tissue cells. hG-CSF is used in used to treat anomalies that reder a small number of circulating white blood cells, which may compromise the immune defenses of the affected person. For these reasons, the production of hG-CSF in a bioreactor system using the mammary gland of genetic modified animals is a possibility of adding value to the bovine genetic material and reducing the costs of hG-CSF production in pharmaceutical industry. In this study, we aimed the production of transgenic hG-CSF bovine through the lipofection of bovine primary fibroblasts with an hG-CSF expression cassette and cloning these fibroblasts by the somatic cell nuclear transfer (SCNT) technique. The bovine fibroblasts transfected with the hG-CSF cassette presented a stable insertion of this construct into their genome and were efficiently synchronized to G0/G1 cell cycle stage. The transgenic fibroblasts were cloned by SCNT and produced 103 transferred embryos and 2 pregnancies, one of which reached 7 months of gestation. |
format | Online Article Text |
id | pubmed-6582935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society of Animal Science and Technology |
record_format | MEDLINE/PubMed |
spelling | pubmed-65829352019-07-22 Production of transgenic cattle by somatic cell nuclear transfer (SCNT) with the human granulocyte colony-stimulation factor (hG-CSF) Carvalho, Bruno P. Cunha, Andrielle T. M. Silva, Bianca D. M. Sousa, Regivaldo V. Leme, Ligiane O. Dode, Margot A. N. Melo, Eduardo O. J Anim Sci Technol Research The hG-CSF (human Granulocyte Colony-Stimulating Factor) is a growth and stimulation factor capable of inducing the proliferation of bone marrow cells, several types of leukocytes, among other hematopoietic tissue cells. hG-CSF is used in used to treat anomalies that reder a small number of circulating white blood cells, which may compromise the immune defenses of the affected person. For these reasons, the production of hG-CSF in a bioreactor system using the mammary gland of genetic modified animals is a possibility of adding value to the bovine genetic material and reducing the costs of hG-CSF production in pharmaceutical industry. In this study, we aimed the production of transgenic hG-CSF bovine through the lipofection of bovine primary fibroblasts with an hG-CSF expression cassette and cloning these fibroblasts by the somatic cell nuclear transfer (SCNT) technique. The bovine fibroblasts transfected with the hG-CSF cassette presented a stable insertion of this construct into their genome and were efficiently synchronized to G0/G1 cell cycle stage. The transgenic fibroblasts were cloned by SCNT and produced 103 transferred embryos and 2 pregnancies, one of which reached 7 months of gestation. Korean Society of Animal Science and Technology 2019-03 2019-03-31 /pmc/articles/PMC6582935/ /pubmed/31333863 http://dx.doi.org/10.5187/jast.2019.61.2.61 Text en © Copyright 2019 Korean Society of Animal Science and Technology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Carvalho, Bruno P. Cunha, Andrielle T. M. Silva, Bianca D. M. Sousa, Regivaldo V. Leme, Ligiane O. Dode, Margot A. N. Melo, Eduardo O. Production of transgenic cattle by somatic cell nuclear transfer (SCNT) with the human granulocyte colony-stimulation factor (hG-CSF) |
title | Production of transgenic cattle by somatic cell nuclear transfer
(SCNT) with the human granulocyte colony-stimulation factor
(hG-CSF) |
title_full | Production of transgenic cattle by somatic cell nuclear transfer
(SCNT) with the human granulocyte colony-stimulation factor
(hG-CSF) |
title_fullStr | Production of transgenic cattle by somatic cell nuclear transfer
(SCNT) with the human granulocyte colony-stimulation factor
(hG-CSF) |
title_full_unstemmed | Production of transgenic cattle by somatic cell nuclear transfer
(SCNT) with the human granulocyte colony-stimulation factor
(hG-CSF) |
title_short | Production of transgenic cattle by somatic cell nuclear transfer
(SCNT) with the human granulocyte colony-stimulation factor
(hG-CSF) |
title_sort | production of transgenic cattle by somatic cell nuclear transfer
(scnt) with the human granulocyte colony-stimulation factor
(hg-csf) |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582935/ https://www.ncbi.nlm.nih.gov/pubmed/31333863 http://dx.doi.org/10.5187/jast.2019.61.2.61 |
work_keys_str_mv | AT carvalhobrunop productionoftransgeniccattlebysomaticcellnucleartransferscntwiththehumangranulocytecolonystimulationfactorhgcsf AT cunhaandrielletm productionoftransgeniccattlebysomaticcellnucleartransferscntwiththehumangranulocytecolonystimulationfactorhgcsf AT silvabiancadm productionoftransgeniccattlebysomaticcellnucleartransferscntwiththehumangranulocytecolonystimulationfactorhgcsf AT sousaregivaldov productionoftransgeniccattlebysomaticcellnucleartransferscntwiththehumangranulocytecolonystimulationfactorhgcsf AT lemeligianeo productionoftransgeniccattlebysomaticcellnucleartransferscntwiththehumangranulocytecolonystimulationfactorhgcsf AT dodemargotan productionoftransgeniccattlebysomaticcellnucleartransferscntwiththehumangranulocytecolonystimulationfactorhgcsf AT meloeduardoo productionoftransgeniccattlebysomaticcellnucleartransferscntwiththehumangranulocytecolonystimulationfactorhgcsf |