Cargando…

Maintaining bovine satellite cells stemness through p38 pathway

Isolating and maintaining the appropriate stem cell for large scale cell culture is essential in tissue engineering or food production. For bovine satellite cells an optimized isolation and purification protocol is lacking and there is also no detailed understanding on the factors that maintain stem...

Descripción completa

Detalles Bibliográficos
Autores principales: Ding, Shijie, Swennen, G. N. M, Messmer, Tobias, Gagliardi, Mick, Molin, Daniël G. M., Li, Chunbao, Zhou, Guanghong, Post, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050236/
https://www.ncbi.nlm.nih.gov/pubmed/30018348
http://dx.doi.org/10.1038/s41598-018-28746-7
_version_ 1783340289875771392
author Ding, Shijie
Swennen, G. N. M
Messmer, Tobias
Gagliardi, Mick
Molin, Daniël G. M.
Li, Chunbao
Zhou, Guanghong
Post, Mark J.
author_facet Ding, Shijie
Swennen, G. N. M
Messmer, Tobias
Gagliardi, Mick
Molin, Daniël G. M.
Li, Chunbao
Zhou, Guanghong
Post, Mark J.
author_sort Ding, Shijie
collection PubMed
description Isolating and maintaining the appropriate stem cell for large scale cell culture is essential in tissue engineering or food production. For bovine satellite cells an optimized isolation and purification protocol is lacking and there is also no detailed understanding on the factors that maintain stemness of these cells. Here, we set up a fluorescence-activated cell sorting strategy to enrich bovine satellite cells. We found that p38-MAPK signalling is activated and PAX7 expression is gradually lost during satellite cell proliferation. The p38 inhibitor (SB203580) treatment maintained PAX7 expression but inhibited the fusion of satellite cells in a concentration-dependent way in short-term incubation. The mechanism of p38 inhibition was confirmed by inhibiting canonical p38 signalling, i.e. HSP27. Long-term culture with an appropriate concentration of p38i enhanced the proliferation and PAX7 expression, while the differentiation capacity recovered and was enhanced compared to vehicle control. These studies indicate that bovine satellite cells maintenance depends on cell purity and p38 MAPK signalling. Inhibition of p38 MAPK signaling is a promising strategy to facilitate large scale cell expansion of primary cells for tissue engineering and cultured meat purposes.
format Online
Article
Text
id pubmed-6050236
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-60502362018-07-19 Maintaining bovine satellite cells stemness through p38 pathway Ding, Shijie Swennen, G. N. M Messmer, Tobias Gagliardi, Mick Molin, Daniël G. M. Li, Chunbao Zhou, Guanghong Post, Mark J. Sci Rep Article Isolating and maintaining the appropriate stem cell for large scale cell culture is essential in tissue engineering or food production. For bovine satellite cells an optimized isolation and purification protocol is lacking and there is also no detailed understanding on the factors that maintain stemness of these cells. Here, we set up a fluorescence-activated cell sorting strategy to enrich bovine satellite cells. We found that p38-MAPK signalling is activated and PAX7 expression is gradually lost during satellite cell proliferation. The p38 inhibitor (SB203580) treatment maintained PAX7 expression but inhibited the fusion of satellite cells in a concentration-dependent way in short-term incubation. The mechanism of p38 inhibition was confirmed by inhibiting canonical p38 signalling, i.e. HSP27. Long-term culture with an appropriate concentration of p38i enhanced the proliferation and PAX7 expression, while the differentiation capacity recovered and was enhanced compared to vehicle control. These studies indicate that bovine satellite cells maintenance depends on cell purity and p38 MAPK signalling. Inhibition of p38 MAPK signaling is a promising strategy to facilitate large scale cell expansion of primary cells for tissue engineering and cultured meat purposes. Nature Publishing Group UK 2018-07-17 /pmc/articles/PMC6050236/ /pubmed/30018348 http://dx.doi.org/10.1038/s41598-018-28746-7 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Ding, Shijie
Swennen, G. N. M
Messmer, Tobias
Gagliardi, Mick
Molin, Daniël G. M.
Li, Chunbao
Zhou, Guanghong
Post, Mark J.
Maintaining bovine satellite cells stemness through p38 pathway
title Maintaining bovine satellite cells stemness through p38 pathway
title_full Maintaining bovine satellite cells stemness through p38 pathway
title_fullStr Maintaining bovine satellite cells stemness through p38 pathway
title_full_unstemmed Maintaining bovine satellite cells stemness through p38 pathway
title_short Maintaining bovine satellite cells stemness through p38 pathway
title_sort maintaining bovine satellite cells stemness through p38 pathway
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6050236/
https://www.ncbi.nlm.nih.gov/pubmed/30018348
http://dx.doi.org/10.1038/s41598-018-28746-7
work_keys_str_mv AT dingshijie maintainingbovinesatellitecellsstemnessthroughp38pathway
AT swennengnm maintainingbovinesatellitecellsstemnessthroughp38pathway
AT messmertobias maintainingbovinesatellitecellsstemnessthroughp38pathway
AT gagliardimick maintainingbovinesatellitecellsstemnessthroughp38pathway
AT molindanielgm maintainingbovinesatellitecellsstemnessthroughp38pathway
AT lichunbao maintainingbovinesatellitecellsstemnessthroughp38pathway
AT zhouguanghong maintainingbovinesatellitecellsstemnessthroughp38pathway
AT postmarkj maintainingbovinesatellitecellsstemnessthroughp38pathway