Characterization of cell cycle and apoptosis in Chinese hamster ovary cell culture using flow cytometry for bioprocess monitoring
Chinese hamster ovary (CHO) cells are by far the most important mammalian cell lines used for producing antibodies and other therapeutic proteins. It is critical to fully understand their physiological conditions during a bioprocess in order to achieve the highest productivity and the desired produc...
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Veröffentlicht in: | Biotechnology progress 2022-01, Vol.38 (1), p.e3211-n/a |
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creator | Ji, Xiaodan Lee, Young Je Eyster, Tom Parrillo, Alexis Galosy, Sybille Ao, Zhaohui Patel, Pramthesh Zhu, Yuan |
description | Chinese hamster ovary (CHO) cells are by far the most important mammalian cell lines used for producing antibodies and other therapeutic proteins. It is critical to fully understand their physiological conditions during a bioprocess in order to achieve the highest productivity and the desired product quality. Flow cytometry technology possesses unique advantages for measuring multiple cellular attributes for a given cell and examining changes in cell culture heterogeneity over time that can be used as metrics for enhanced process understanding and control strategy. Flow cytometry‐based assays were utilized to examine the progression of cell cycle and apoptosis in three case studies using different antibody‐producing CHO cell lines in both fed‐batch and perfusion bioprocesses. In our case studies, we found that G0/G1 phase distribution and early apoptosis accumulation responded to subtle changes in culture conditions, such as pH shifting or momentary glucose depletion. In a perfusion process, flow cytometry provided an insightful understanding of the cell physiological status under a hypothermic condition. More importantly, these changes in cell cycle and apoptosis were not detected by a routine trypan blue exclusion‐based cell counting and viability measurement. In summary, integration of flow cytometry into bioprocesses as a process analytical technology tool can be beneficial for establishing optimum process conditions and process control. |
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It is critical to fully understand their physiological conditions during a bioprocess in order to achieve the highest productivity and the desired product quality. Flow cytometry technology possesses unique advantages for measuring multiple cellular attributes for a given cell and examining changes in cell culture heterogeneity over time that can be used as metrics for enhanced process understanding and control strategy. Flow cytometry‐based assays were utilized to examine the progression of cell cycle and apoptosis in three case studies using different antibody‐producing CHO cell lines in both fed‐batch and perfusion bioprocesses. In our case studies, we found that G0/G1 phase distribution and early apoptosis accumulation responded to subtle changes in culture conditions, such as pH shifting or momentary glucose depletion. In a perfusion process, flow cytometry provided an insightful understanding of the cell physiological status under a hypothermic condition. More importantly, these changes in cell cycle and apoptosis were not detected by a routine trypan blue exclusion‐based cell counting and viability measurement. 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It is critical to fully understand their physiological conditions during a bioprocess in order to achieve the highest productivity and the desired product quality. Flow cytometry technology possesses unique advantages for measuring multiple cellular attributes for a given cell and examining changes in cell culture heterogeneity over time that can be used as metrics for enhanced process understanding and control strategy. Flow cytometry‐based assays were utilized to examine the progression of cell cycle and apoptosis in three case studies using different antibody‐producing CHO cell lines in both fed‐batch and perfusion bioprocesses. In our case studies, we found that G0/G1 phase distribution and early apoptosis accumulation responded to subtle changes in culture conditions, such as pH shifting or momentary glucose depletion. In a perfusion process, flow cytometry provided an insightful understanding of the cell physiological status under a hypothermic condition. 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In summary, integration of flow cytometry into bioprocesses as a process analytical technology tool can be beneficial for establishing optimum process conditions and process control.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Apoptosis</subject><subject>Batch Cell Culture Techniques</subject><subject>Bioreactors</subject><subject>Case studies</subject><subject>Cell culture</subject><subject>Cell Culture Techniques</subject><subject>Cell Cycle</subject><subject>Cell lines</subject><subject>CHO Cells</subject><subject>Cricetinae</subject><subject>Cricetulus</subject><subject>Depletion</subject><subject>fed‐batch process</subject><subject>Flow Cytometry</subject><subject>G1 phase</subject><subject>Heterogeneity</subject><subject>Ovaries</subject><subject>Perfusion</subject><subject>perfusion process</subject><subject>Phase distribution</subject><subject>Physiology</subject><subject>process analytical technology</subject><subject>Process control</subject><subject>Process controls</subject><subject>Technology assessment</subject><issn>8756-7938</issn><issn>1520-6033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1DAURq0KRKeFRV-gssSGLtL6J3biJYxoi1QJhMracuJrxlUSp7ZDNex4czydgQUSK9_Fucef7ofQGSWXlBB21eU5XnJG6RFaUcFIJQnnL9CqbYSsGsXbY3SS0gMhpCWSvULHvBa1EoKt0K_1xkTTZ4j-p8k-TDg43MMw4H7bD4DNZLGZw5xD8gn7Ca83foIEeGPGVLZw-GHi9rCxDHmJgJfkp-_YDeGpSHIYIRfChYg7H-YYekgJj2HyOcQCvkYvnRkSvDm8p-jb9cf79W119_nm0_r9XdVzwWlVW8JZx3unhKqtUI7RhjkLyirRMV4GqVrVUmKpAGisbEHVqnGyri3tupqfond7b4nwuEDKevRpl9tMEJakmWgEb8oReUHf_oM-hCVOJZ1mkpVfiJCyUBd7qo8hpQhOz9GP5RqaEr3rRe960bteCnt-MC7dCPYv-aeIAlztgSc_wPb_Jv3h_svXZ-VvtmyZrQ</recordid><startdate>202201</startdate><enddate>202201</enddate><creator>Ji, Xiaodan</creator><creator>Lee, Young Je</creator><creator>Eyster, Tom</creator><creator>Parrillo, Alexis</creator><creator>Galosy, Sybille</creator><creator>Ao, Zhaohui</creator><creator>Patel, Pramthesh</creator><creator>Zhu, Yuan</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1317-5881</orcidid><orcidid>https://orcid.org/0000-0002-1333-5163</orcidid></search><sort><creationdate>202201</creationdate><title>Characterization of cell cycle and apoptosis in Chinese hamster ovary cell culture using flow cytometry for bioprocess monitoring</title><author>Ji, Xiaodan ; Lee, Young Je ; Eyster, Tom ; Parrillo, Alexis ; Galosy, Sybille ; Ao, Zhaohui ; Patel, Pramthesh ; Zhu, Yuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3531-4d032b3cf9594d59f2172fde9d95b23de96989810d15ee7d68e9497f644d1bb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Apoptosis</topic><topic>Batch Cell Culture Techniques</topic><topic>Bioreactors</topic><topic>Case studies</topic><topic>Cell culture</topic><topic>Cell Culture Techniques</topic><topic>Cell Cycle</topic><topic>Cell lines</topic><topic>CHO Cells</topic><topic>Cricetinae</topic><topic>Cricetulus</topic><topic>Depletion</topic><topic>fed‐batch process</topic><topic>Flow Cytometry</topic><topic>G1 phase</topic><topic>Heterogeneity</topic><topic>Ovaries</topic><topic>Perfusion</topic><topic>perfusion process</topic><topic>Phase distribution</topic><topic>Physiology</topic><topic>process analytical technology</topic><topic>Process control</topic><topic>Process controls</topic><topic>Technology assessment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ji, Xiaodan</creatorcontrib><creatorcontrib>Lee, Young Je</creatorcontrib><creatorcontrib>Eyster, Tom</creatorcontrib><creatorcontrib>Parrillo, Alexis</creatorcontrib><creatorcontrib>Galosy, Sybille</creatorcontrib><creatorcontrib>Ao, Zhaohui</creatorcontrib><creatorcontrib>Patel, Pramthesh</creatorcontrib><creatorcontrib>Zhu, Yuan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biotechnology progress</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ji, Xiaodan</au><au>Lee, Young Je</au><au>Eyster, Tom</au><au>Parrillo, Alexis</au><au>Galosy, Sybille</au><au>Ao, Zhaohui</au><au>Patel, Pramthesh</au><au>Zhu, Yuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of cell cycle and apoptosis in Chinese hamster ovary cell culture using flow cytometry for bioprocess monitoring</atitle><jtitle>Biotechnology progress</jtitle><addtitle>Biotechnol Prog</addtitle><date>2022-01</date><risdate>2022</risdate><volume>38</volume><issue>1</issue><spage>e3211</spage><epage>n/a</epage><pages>e3211-n/a</pages><issn>8756-7938</issn><eissn>1520-6033</eissn><abstract>Chinese hamster ovary (CHO) cells are by far the most important mammalian cell lines used for producing antibodies and other therapeutic proteins. It is critical to fully understand their physiological conditions during a bioprocess in order to achieve the highest productivity and the desired product quality. Flow cytometry technology possesses unique advantages for measuring multiple cellular attributes for a given cell and examining changes in cell culture heterogeneity over time that can be used as metrics for enhanced process understanding and control strategy. Flow cytometry‐based assays were utilized to examine the progression of cell cycle and apoptosis in three case studies using different antibody‐producing CHO cell lines in both fed‐batch and perfusion bioprocesses. In our case studies, we found that G0/G1 phase distribution and early apoptosis accumulation responded to subtle changes in culture conditions, such as pH shifting or momentary glucose depletion. In a perfusion process, flow cytometry provided an insightful understanding of the cell physiological status under a hypothermic condition. 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subjects | Animals Antibodies Apoptosis Batch Cell Culture Techniques Bioreactors Case studies Cell culture Cell Culture Techniques Cell Cycle Cell lines CHO Cells Cricetinae Cricetulus Depletion fed‐batch process Flow Cytometry G1 phase Heterogeneity Ovaries Perfusion perfusion process Phase distribution Physiology process analytical technology Process control Process controls Technology assessment |
title | Characterization of cell cycle and apoptosis in Chinese hamster ovary cell culture using flow cytometry for bioprocess monitoring |
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