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Serum-free media for the growth of primary bovine myoblasts
The demand for meat is expected to exceed production capacity by livestock in the coming decennia. Therefore, cultured beef might be a viable alternative to traditional livestock-derived beef. One of the problems however is the sustainability of cultured beef through the use of fetal bovine serum. W...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002633/ https://www.ncbi.nlm.nih.gov/pubmed/31884572 http://dx.doi.org/10.1007/s10616-019-00361-y |
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author | Kolkmann, A. M. Post, M. J. Rutjens, M. A. M. van Essen, A. L. M. Moutsatsou, P. |
author_facet | Kolkmann, A. M. Post, M. J. Rutjens, M. A. M. van Essen, A. L. M. Moutsatsou, P. |
author_sort | Kolkmann, A. M. |
collection | PubMed |
description | The demand for meat is expected to exceed production capacity by livestock in the coming decennia. Therefore, cultured beef might be a viable alternative to traditional livestock-derived beef. One of the problems however is the sustainability of cultured beef through the use of fetal bovine serum. We aimed to identify a serum-free medium or a serum-replacement that is as effective as the current method used for culturing bovine myoblasts. Cells were harvested from a female Blanc Bleu Belge cow and myoblasts were subsequently isolated. Cells were cultured in either Advanced DMEM containing 20% FBS and 10% HS or one of the chemically-defined, serum-free media for 6 days. MTS was used as a measure of cell proliferation at day 1, 4 or 6 and microscopic pictures were taken to assess cell morphology. FBM™, TesR™ and Essential 8™ are commercially available xeno-free media developed for human PSCs and fibroblasts, with the highest potential to sustain bovine myoblast proliferation. Of the supplements tested, XenoFree™ and a custom-prepared growth factor mix failed to stimulate cell proliferation. LipoGro™ stimulated cell proliferation in some cases but also changed the phenotype of myoblasts to an adipocyte-like phenotype. We conclude that serum-free media stimulate exponential cell expansion, albeit not to the extent of the current growth medium containing up to 30% serum. Further research is needed to investigate whether prolonged cell culture or an adaptation period could further increase cell proliferation. |
format | Online Article Text |
id | pubmed-7002633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-70026332020-02-25 Serum-free media for the growth of primary bovine myoblasts Kolkmann, A. M. Post, M. J. Rutjens, M. A. M. van Essen, A. L. M. Moutsatsou, P. Cytotechnology Original Article The demand for meat is expected to exceed production capacity by livestock in the coming decennia. Therefore, cultured beef might be a viable alternative to traditional livestock-derived beef. One of the problems however is the sustainability of cultured beef through the use of fetal bovine serum. We aimed to identify a serum-free medium or a serum-replacement that is as effective as the current method used for culturing bovine myoblasts. Cells were harvested from a female Blanc Bleu Belge cow and myoblasts were subsequently isolated. Cells were cultured in either Advanced DMEM containing 20% FBS and 10% HS or one of the chemically-defined, serum-free media for 6 days. MTS was used as a measure of cell proliferation at day 1, 4 or 6 and microscopic pictures were taken to assess cell morphology. FBM™, TesR™ and Essential 8™ are commercially available xeno-free media developed for human PSCs and fibroblasts, with the highest potential to sustain bovine myoblast proliferation. Of the supplements tested, XenoFree™ and a custom-prepared growth factor mix failed to stimulate cell proliferation. LipoGro™ stimulated cell proliferation in some cases but also changed the phenotype of myoblasts to an adipocyte-like phenotype. We conclude that serum-free media stimulate exponential cell expansion, albeit not to the extent of the current growth medium containing up to 30% serum. Further research is needed to investigate whether prolonged cell culture or an adaptation period could further increase cell proliferation. Springer Netherlands 2019-12-28 2020-02 /pmc/articles/PMC7002633/ /pubmed/31884572 http://dx.doi.org/10.1007/s10616-019-00361-y Text en © The Author(s) 2019 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/. |
spellingShingle | Original Article Kolkmann, A. M. Post, M. J. Rutjens, M. A. M. van Essen, A. L. M. Moutsatsou, P. Serum-free media for the growth of primary bovine myoblasts |
title | Serum-free media for the growth of primary bovine myoblasts |
title_full | Serum-free media for the growth of primary bovine myoblasts |
title_fullStr | Serum-free media for the growth of primary bovine myoblasts |
title_full_unstemmed | Serum-free media for the growth of primary bovine myoblasts |
title_short | Serum-free media for the growth of primary bovine myoblasts |
title_sort | serum-free media for the growth of primary bovine myoblasts |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002633/ https://www.ncbi.nlm.nih.gov/pubmed/31884572 http://dx.doi.org/10.1007/s10616-019-00361-y |
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