Cargando…
Quantification of the dynamics of population heterogeneities in CHO cultures with stably integrated fluorescent markers
Cell population heterogeneities and their changes in mammalian cell culture processes are still not well characterized. In this study, the formation and dynamics of cell population heterogeneities were investigated with flow cytometry and stably integrated fluorescent markers based on the lentiviral...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072063/ https://www.ncbi.nlm.nih.gov/pubmed/32130440 http://dx.doi.org/10.1007/s00216-020-02401-5 |
_version_ | 1783506318419558400 |
---|---|
author | Möller, Johannes Rosenberg, Marcel Riecken, Kristoffer Pörtner, Ralf Zeng, An-Ping Jandt, Uwe |
author_facet | Möller, Johannes Rosenberg, Marcel Riecken, Kristoffer Pörtner, Ralf Zeng, An-Ping Jandt, Uwe |
author_sort | Möller, Johannes |
collection | PubMed |
description | Cell population heterogeneities and their changes in mammalian cell culture processes are still not well characterized. In this study, the formation and dynamics of cell population heterogeneities were investigated with flow cytometry and stably integrated fluorescent markers based on the lentiviral gene ontology (LeGO) vector system. To achieve this, antibody-producing CHO cells were transduced with different LeGO vectors to stably express single or multiple fluorescent proteins. This enables the tracking of the transduced populations and is discussed in two case studies from the field of bioprocess engineering: In case study I, cells were co-transduced to express red, green, and blue fluorescent proteins and the development of sub-populations and expression heterogeneities were investigated in high passage cultivations (total 130 days). The formation of a fast-growing and more productive population was observed with a simultaneous increase in cell density and product titer. In case study II, different preculture growth phases and their influence on the population dynamics were investigated in mixed batch cultures with flow cytometry (offline and automated). Four cell line derivatives, each expressing a different fluorescent protein, were generated and cultivated for different time intervals, corresponding to different growth phases. Mixed cultures were inoculated from them, and changes in the composition of the cell populations were observed during the first 48 h of cultivation with reduced process productivity. In summary, we showed how the dynamics of population heterogeneities can be characterized. This represents a novel approach to investigate the dynamics of cell population heterogeneities under near-physiological conditions with changing productivity in mammalian cell culture processes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-020-02401-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7072063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-70720632020-03-23 Quantification of the dynamics of population heterogeneities in CHO cultures with stably integrated fluorescent markers Möller, Johannes Rosenberg, Marcel Riecken, Kristoffer Pörtner, Ralf Zeng, An-Ping Jandt, Uwe Anal Bioanal Chem Paper in Forefront Cell population heterogeneities and their changes in mammalian cell culture processes are still not well characterized. In this study, the formation and dynamics of cell population heterogeneities were investigated with flow cytometry and stably integrated fluorescent markers based on the lentiviral gene ontology (LeGO) vector system. To achieve this, antibody-producing CHO cells were transduced with different LeGO vectors to stably express single or multiple fluorescent proteins. This enables the tracking of the transduced populations and is discussed in two case studies from the field of bioprocess engineering: In case study I, cells were co-transduced to express red, green, and blue fluorescent proteins and the development of sub-populations and expression heterogeneities were investigated in high passage cultivations (total 130 days). The formation of a fast-growing and more productive population was observed with a simultaneous increase in cell density and product titer. In case study II, different preculture growth phases and their influence on the population dynamics were investigated in mixed batch cultures with flow cytometry (offline and automated). Four cell line derivatives, each expressing a different fluorescent protein, were generated and cultivated for different time intervals, corresponding to different growth phases. Mixed cultures were inoculated from them, and changes in the composition of the cell populations were observed during the first 48 h of cultivation with reduced process productivity. In summary, we showed how the dynamics of population heterogeneities can be characterized. This represents a novel approach to investigate the dynamics of cell population heterogeneities under near-physiological conditions with changing productivity in mammalian cell culture processes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-020-02401-5) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-03-04 2020 /pmc/articles/PMC7072063/ /pubmed/32130440 http://dx.doi.org/10.1007/s00216-020-02401-5 Text en © The Author(s) 2020 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 | Paper in Forefront Möller, Johannes Rosenberg, Marcel Riecken, Kristoffer Pörtner, Ralf Zeng, An-Ping Jandt, Uwe Quantification of the dynamics of population heterogeneities in CHO cultures with stably integrated fluorescent markers |
title | Quantification of the dynamics of population heterogeneities in CHO cultures with stably integrated fluorescent markers |
title_full | Quantification of the dynamics of population heterogeneities in CHO cultures with stably integrated fluorescent markers |
title_fullStr | Quantification of the dynamics of population heterogeneities in CHO cultures with stably integrated fluorescent markers |
title_full_unstemmed | Quantification of the dynamics of population heterogeneities in CHO cultures with stably integrated fluorescent markers |
title_short | Quantification of the dynamics of population heterogeneities in CHO cultures with stably integrated fluorescent markers |
title_sort | quantification of the dynamics of population heterogeneities in cho cultures with stably integrated fluorescent markers |
topic | Paper in Forefront |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072063/ https://www.ncbi.nlm.nih.gov/pubmed/32130440 http://dx.doi.org/10.1007/s00216-020-02401-5 |
work_keys_str_mv | AT mollerjohannes quantificationofthedynamicsofpopulationheterogeneitiesinchocultureswithstablyintegratedfluorescentmarkers AT rosenbergmarcel quantificationofthedynamicsofpopulationheterogeneitiesinchocultureswithstablyintegratedfluorescentmarkers AT rieckenkristoffer quantificationofthedynamicsofpopulationheterogeneitiesinchocultureswithstablyintegratedfluorescentmarkers AT portnerralf quantificationofthedynamicsofpopulationheterogeneitiesinchocultureswithstablyintegratedfluorescentmarkers AT zenganping quantificationofthedynamicsofpopulationheterogeneitiesinchocultureswithstablyintegratedfluorescentmarkers AT jandtuwe quantificationofthedynamicsofpopulationheterogeneitiesinchocultureswithstablyintegratedfluorescentmarkers |