Cargando…

Single-Cell Analysis of CHO Cells Reveals Clonal Heterogeneity in Hyperosmolality-Induced Stress Response

Hyperosmolality can occur during industrial fed-batch cultivation processes of Chinese hamster ovary (CHO) cells as highly concentrated feed and base solutions are added to replenish nutrients and regulate pH values. Some effects of hyperosmolality, such as increased cell size and growth inhibition,...

Descripción completa

Detalles Bibliográficos
Autores principales: Romanova, Nadiya, Schmitz, Julian, Strakeljahn, Marie, Grünberger, Alexander, Bahnemann, Janina, Noll, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9179406/
https://www.ncbi.nlm.nih.gov/pubmed/35681457
http://dx.doi.org/10.3390/cells11111763
_version_ 1784723266076672000
author Romanova, Nadiya
Schmitz, Julian
Strakeljahn, Marie
Grünberger, Alexander
Bahnemann, Janina
Noll, Thomas
author_facet Romanova, Nadiya
Schmitz, Julian
Strakeljahn, Marie
Grünberger, Alexander
Bahnemann, Janina
Noll, Thomas
author_sort Romanova, Nadiya
collection PubMed
description Hyperosmolality can occur during industrial fed-batch cultivation processes of Chinese hamster ovary (CHO) cells as highly concentrated feed and base solutions are added to replenish nutrients and regulate pH values. Some effects of hyperosmolality, such as increased cell size and growth inhibition, have been elucidated by previous research, but the impact of hyperosmolality and the specific effects of the added osmotic-active reagents have rarely been disentangled. In this study, CHO cells were exposed to four osmotic conditions between 300 mOsm/kg (physiologic condition) and 530 mOsm/kg (extreme hyperosmolality) caused by the addition of either high-glucose-supplemented industrial feed or mannitol as an osmotic control. We present novel single-cell cultivation data revealing heterogeneity in mass gain and cell division in response to these treatments. Exposure to extreme mannitol-induced hyperosmolality and to high-glucose-oversupplemented feed causes cell cycle termination, mtDNA damage, and mitochondrial membrane depolarization, which hints at the onset of premature stress-induced senescence. Thus, this study shows that both mannitol-induced hyperosmolality (530 mOsm/kg) and glucose overfeeding induce severe negative effects on cell growth and mitochondrial activity; therefore, they need to be considered during process development for commercial production.
format Online
Article
Text
id pubmed-9179406
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-91794062022-06-10 Single-Cell Analysis of CHO Cells Reveals Clonal Heterogeneity in Hyperosmolality-Induced Stress Response Romanova, Nadiya Schmitz, Julian Strakeljahn, Marie Grünberger, Alexander Bahnemann, Janina Noll, Thomas Cells Article Hyperosmolality can occur during industrial fed-batch cultivation processes of Chinese hamster ovary (CHO) cells as highly concentrated feed and base solutions are added to replenish nutrients and regulate pH values. Some effects of hyperosmolality, such as increased cell size and growth inhibition, have been elucidated by previous research, but the impact of hyperosmolality and the specific effects of the added osmotic-active reagents have rarely been disentangled. In this study, CHO cells were exposed to four osmotic conditions between 300 mOsm/kg (physiologic condition) and 530 mOsm/kg (extreme hyperosmolality) caused by the addition of either high-glucose-supplemented industrial feed or mannitol as an osmotic control. We present novel single-cell cultivation data revealing heterogeneity in mass gain and cell division in response to these treatments. Exposure to extreme mannitol-induced hyperosmolality and to high-glucose-oversupplemented feed causes cell cycle termination, mtDNA damage, and mitochondrial membrane depolarization, which hints at the onset of premature stress-induced senescence. Thus, this study shows that both mannitol-induced hyperosmolality (530 mOsm/kg) and glucose overfeeding induce severe negative effects on cell growth and mitochondrial activity; therefore, they need to be considered during process development for commercial production. MDPI 2022-05-27 /pmc/articles/PMC9179406/ /pubmed/35681457 http://dx.doi.org/10.3390/cells11111763 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Romanova, Nadiya
Schmitz, Julian
Strakeljahn, Marie
Grünberger, Alexander
Bahnemann, Janina
Noll, Thomas
Single-Cell Analysis of CHO Cells Reveals Clonal Heterogeneity in Hyperosmolality-Induced Stress Response
title Single-Cell Analysis of CHO Cells Reveals Clonal Heterogeneity in Hyperosmolality-Induced Stress Response
title_full Single-Cell Analysis of CHO Cells Reveals Clonal Heterogeneity in Hyperosmolality-Induced Stress Response
title_fullStr Single-Cell Analysis of CHO Cells Reveals Clonal Heterogeneity in Hyperosmolality-Induced Stress Response
title_full_unstemmed Single-Cell Analysis of CHO Cells Reveals Clonal Heterogeneity in Hyperosmolality-Induced Stress Response
title_short Single-Cell Analysis of CHO Cells Reveals Clonal Heterogeneity in Hyperosmolality-Induced Stress Response
title_sort single-cell analysis of cho cells reveals clonal heterogeneity in hyperosmolality-induced stress response
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9179406/
https://www.ncbi.nlm.nih.gov/pubmed/35681457
http://dx.doi.org/10.3390/cells11111763
work_keys_str_mv AT romanovanadiya singlecellanalysisofchocellsrevealsclonalheterogeneityinhyperosmolalityinducedstressresponse
AT schmitzjulian singlecellanalysisofchocellsrevealsclonalheterogeneityinhyperosmolalityinducedstressresponse
AT strakeljahnmarie singlecellanalysisofchocellsrevealsclonalheterogeneityinhyperosmolalityinducedstressresponse
AT grunbergeralexander singlecellanalysisofchocellsrevealsclonalheterogeneityinhyperosmolalityinducedstressresponse
AT bahnemannjanina singlecellanalysisofchocellsrevealsclonalheterogeneityinhyperosmolalityinducedstressresponse
AT nollthomas singlecellanalysisofchocellsrevealsclonalheterogeneityinhyperosmolalityinducedstressresponse