Effects of Cloned Gene Dosage on the Response of Recombinant CHO Cells to Hyperosmotic Pressure in Regard to Cell Growth and Antibody Production
The effect of cloned gene dosage on growth and product formation under hyperosmotic conditions has been studied using recombinant Chinese hamster ovary (rCHO) cell lines producing chimeric antibody. Batch cultures of four rCHO cell lines carrying different numbers of antibody gene copies were carrie...
Gespeichert in:
Veröffentlicht in: | Biotechnology progress 2001-11, Vol.17 (6), p.993-999 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 999 |
---|---|
container_issue | 6 |
container_start_page | 993 |
container_title | Biotechnology progress |
container_volume | 17 |
creator | Ryu, Joon Soo Lee, Moon Sue Lee, Gyun Min |
description | The effect of cloned gene dosage on growth and product formation under hyperosmotic conditions has been studied using recombinant Chinese hamster ovary (rCHO) cell lines producing chimeric antibody. Batch cultures of four rCHO cell lines carrying different numbers of antibody gene copies were carried out using the hyperosmolar medium. Depending on cloned gene dosage, hyperosmotic pressure decreased specific growth rate (μ) and increased specific antibody productivity (qAb) to a different degree. The cell line with lower cloned gene dosage displayed more significant enhancement in qAb and less reduction in μ at hyperosmolalities. However, the cell line with higher cloned gene dosage still yielded higher maximum antibody concentration at hyperosmolality up to 469 mOsm/kg. Northern blot analysis showed a positive relationship between immunoglobulin mRNA level per cell and qAb, indicating that transcriptional regulation was involved in the response of rCHO cells to hyperosmotic pressure. Cell cycle analysis showed that hyperosmotic pressure induced G1‐phase arrest, suggesting that the increase of cell population in G1‐phase may contribute in part to enhanced
qAb at hyperosmolality. Taken together, although the cell line with lower cloned gene dosage displayed more significant enhancement in qAb at hyperosmolality, the factor that determined the maximum antibody concentration in hyperosmotic rCHO cell cultures was almost exclusively the gene dosage. |
doi_str_mv | 10.1021/bp010116e |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72336875</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18367857</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4876-90eb3086b49547e6c9ebbd9a271f9c184d8f3bfda056551281b156f849a4e2bf3</originalsourceid><addsrcrecordid>eNqF0c1u1DAUBeAIgehQWPACyBuQWATsOP7JsqTtDFKhZRiExMaynes2kNjBTlTmLXhkMsyoXSFW9uI719Y9Wfac4DcEF-StGTDBhHB4kC0IK3DOMaUPs4UUjOeiovIoe5LSd4yxxLx4nB0RIigrKVlkv8-cAzsmFByqu-ChQUvwgE5D0teAgkfjDaA1pCH4BDu1Bht603rtR1SvLlENXZfQGNBqO0AMqQ9ja9FVhJSmCKj1c-Jax2ZHdhYtY7gdb5D2DTrxY2tCs515aCY7tsE_zR453SV4djiPsy_nZ5t6lV9cLt_XJxe5LaXgeYXBUCy5KStWCuC2AmOaSheCuMoSWTbSUeMajRlnjBSSGMK4k2WlSyiMo8fZq_3cIYafE6RR9W2y8_-0hzAlJQpK-bzA_0IiKReSiRm-3kM7byFFcGqIba_jVhGsdj2pu55m--IwdDI9NPfyUMwMXh6ATlZ3Lmpv23TvSsLKqixmh_futu1g--8X1bvN1frvdY7k-0ibRvh1F9Hxh-KCCqa-flyqc_bpdPNBfFbf6B8VYri1</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18367857</pqid></control><display><type>article</type><title>Effects of Cloned Gene Dosage on the Response of Recombinant CHO Cells to Hyperosmotic Pressure in Regard to Cell Growth and Antibody Production</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Ryu, Joon Soo ; Lee, Moon Sue ; Lee, Gyun Min</creator><creatorcontrib>Ryu, Joon Soo ; Lee, Moon Sue ; Lee, Gyun Min</creatorcontrib><description>The effect of cloned gene dosage on growth and product formation under hyperosmotic conditions has been studied using recombinant Chinese hamster ovary (rCHO) cell lines producing chimeric antibody. Batch cultures of four rCHO cell lines carrying different numbers of antibody gene copies were carried out using the hyperosmolar medium. Depending on cloned gene dosage, hyperosmotic pressure decreased specific growth rate (μ) and increased specific antibody productivity (qAb) to a different degree. The cell line with lower cloned gene dosage displayed more significant enhancement in qAb and less reduction in μ at hyperosmolalities. However, the cell line with higher cloned gene dosage still yielded higher maximum antibody concentration at hyperosmolality up to 469 mOsm/kg. Northern blot analysis showed a positive relationship between immunoglobulin mRNA level per cell and qAb, indicating that transcriptional regulation was involved in the response of rCHO cells to hyperosmotic pressure. Cell cycle analysis showed that hyperosmotic pressure induced G1‐phase arrest, suggesting that the increase of cell population in G1‐phase may contribute in part to enhanced
qAb at hyperosmolality. Taken together, although the cell line with lower cloned gene dosage displayed more significant enhancement in qAb at hyperosmolality, the factor that determined the maximum antibody concentration in hyperosmotic rCHO cell cultures was almost exclusively the gene dosage.</description><identifier>ISSN: 8756-7938</identifier><identifier>EISSN: 1520-6033</identifier><identifier>DOI: 10.1021/bp010116e</identifier><identifier>PMID: 11735431</identifier><identifier>CODEN: BIPRET</identifier><language>eng</language><publisher>USA: American Chemical Society</publisher><subject>Animals ; Antibody Formation - physiology ; Biological and medical sciences ; Biotechnology ; Blotting, Northern ; Cell Cycle ; Cell Division - physiology ; CHO Cells - cytology ; CHO Cells - metabolism ; Cloning, Molecular ; Cricetinae ; Culture Media ; DNA - biosynthesis ; Fundamental and applied biological sciences. Psychology ; Gene Dosage ; Glucose - metabolism ; Health. Pharmaceutical industry ; Industrial applications and implications. Economical aspects ; Lactic Acid - metabolism ; Monoclonal antibodies ; Osmotic Pressure ; Production of active biomolecules ; Recombinant Proteins - biosynthesis ; Recombinant Proteins - genetics ; RNA, Messenger - biosynthesis ; Tissue Engineering</subject><ispartof>Biotechnology progress, 2001-11, Vol.17 (6), p.993-999</ispartof><rights>Copyright © 2001 American Institute of Chemical Engineers (AIChE)</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4876-90eb3086b49547e6c9ebbd9a271f9c184d8f3bfda056551281b156f849a4e2bf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1021%2Fbp010116e$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1021%2Fbp010116e$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14154942$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11735431$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ryu, Joon Soo</creatorcontrib><creatorcontrib>Lee, Moon Sue</creatorcontrib><creatorcontrib>Lee, Gyun Min</creatorcontrib><title>Effects of Cloned Gene Dosage on the Response of Recombinant CHO Cells to Hyperosmotic Pressure in Regard to Cell Growth and Antibody Production</title><title>Biotechnology progress</title><addtitle>Biotechnol Progress</addtitle><description>The effect of cloned gene dosage on growth and product formation under hyperosmotic conditions has been studied using recombinant Chinese hamster ovary (rCHO) cell lines producing chimeric antibody. Batch cultures of four rCHO cell lines carrying different numbers of antibody gene copies were carried out using the hyperosmolar medium. Depending on cloned gene dosage, hyperosmotic pressure decreased specific growth rate (μ) and increased specific antibody productivity (qAb) to a different degree. The cell line with lower cloned gene dosage displayed more significant enhancement in qAb and less reduction in μ at hyperosmolalities. However, the cell line with higher cloned gene dosage still yielded higher maximum antibody concentration at hyperosmolality up to 469 mOsm/kg. Northern blot analysis showed a positive relationship between immunoglobulin mRNA level per cell and qAb, indicating that transcriptional regulation was involved in the response of rCHO cells to hyperosmotic pressure. Cell cycle analysis showed that hyperosmotic pressure induced G1‐phase arrest, suggesting that the increase of cell population in G1‐phase may contribute in part to enhanced
qAb at hyperosmolality. Taken together, although the cell line with lower cloned gene dosage displayed more significant enhancement in qAb at hyperosmolality, the factor that determined the maximum antibody concentration in hyperosmotic rCHO cell cultures was almost exclusively the gene dosage.</description><subject>Animals</subject><subject>Antibody Formation - physiology</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Blotting, Northern</subject><subject>Cell Cycle</subject><subject>Cell Division - physiology</subject><subject>CHO Cells - cytology</subject><subject>CHO Cells - metabolism</subject><subject>Cloning, Molecular</subject><subject>Cricetinae</subject><subject>Culture Media</subject><subject>DNA - biosynthesis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Dosage</subject><subject>Glucose - metabolism</subject><subject>Health. Pharmaceutical industry</subject><subject>Industrial applications and implications. Economical aspects</subject><subject>Lactic Acid - metabolism</subject><subject>Monoclonal antibodies</subject><subject>Osmotic Pressure</subject><subject>Production of active biomolecules</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Recombinant Proteins - genetics</subject><subject>RNA, Messenger - biosynthesis</subject><subject>Tissue Engineering</subject><issn>8756-7938</issn><issn>1520-6033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0c1u1DAUBeAIgehQWPACyBuQWATsOP7JsqTtDFKhZRiExMaynes2kNjBTlTmLXhkMsyoXSFW9uI719Y9Wfac4DcEF-StGTDBhHB4kC0IK3DOMaUPs4UUjOeiovIoe5LSd4yxxLx4nB0RIigrKVlkv8-cAzsmFByqu-ChQUvwgE5D0teAgkfjDaA1pCH4BDu1Bht603rtR1SvLlENXZfQGNBqO0AMqQ9ja9FVhJSmCKj1c-Jax2ZHdhYtY7gdb5D2DTrxY2tCs515aCY7tsE_zR453SV4djiPsy_nZ5t6lV9cLt_XJxe5LaXgeYXBUCy5KStWCuC2AmOaSheCuMoSWTbSUeMajRlnjBSSGMK4k2WlSyiMo8fZq_3cIYafE6RR9W2y8_-0hzAlJQpK-bzA_0IiKReSiRm-3kM7byFFcGqIba_jVhGsdj2pu55m--IwdDI9NPfyUMwMXh6ATlZ3Lmpv23TvSsLKqixmh_futu1g--8X1bvN1frvdY7k-0ibRvh1F9Hxh-KCCqa-flyqc_bpdPNBfFbf6B8VYri1</recordid><startdate>20011101</startdate><enddate>20011101</enddate><creator>Ryu, Joon Soo</creator><creator>Lee, Moon Sue</creator><creator>Lee, Gyun Min</creator><general>American Chemical Society</general><general>American Institute of Chemical Engineers</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20011101</creationdate><title>Effects of Cloned Gene Dosage on the Response of Recombinant CHO Cells to Hyperosmotic Pressure in Regard to Cell Growth and Antibody Production</title><author>Ryu, Joon Soo ; Lee, Moon Sue ; Lee, Gyun Min</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4876-90eb3086b49547e6c9ebbd9a271f9c184d8f3bfda056551281b156f849a4e2bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Antibody Formation - physiology</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Blotting, Northern</topic><topic>Cell Cycle</topic><topic>Cell Division - physiology</topic><topic>CHO Cells - cytology</topic><topic>CHO Cells - metabolism</topic><topic>Cloning, Molecular</topic><topic>Cricetinae</topic><topic>Culture Media</topic><topic>DNA - biosynthesis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Dosage</topic><topic>Glucose - metabolism</topic><topic>Health. Pharmaceutical industry</topic><topic>Industrial applications and implications. Economical aspects</topic><topic>Lactic Acid - metabolism</topic><topic>Monoclonal antibodies</topic><topic>Osmotic Pressure</topic><topic>Production of active biomolecules</topic><topic>Recombinant Proteins - biosynthesis</topic><topic>Recombinant Proteins - genetics</topic><topic>RNA, Messenger - biosynthesis</topic><topic>Tissue Engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ryu, Joon Soo</creatorcontrib><creatorcontrib>Lee, Moon Sue</creatorcontrib><creatorcontrib>Lee, Gyun Min</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</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>Ryu, Joon Soo</au><au>Lee, Moon Sue</au><au>Lee, Gyun Min</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Cloned Gene Dosage on the Response of Recombinant CHO Cells to Hyperosmotic Pressure in Regard to Cell Growth and Antibody Production</atitle><jtitle>Biotechnology progress</jtitle><addtitle>Biotechnol Progress</addtitle><date>2001-11-01</date><risdate>2001</risdate><volume>17</volume><issue>6</issue><spage>993</spage><epage>999</epage><pages>993-999</pages><issn>8756-7938</issn><eissn>1520-6033</eissn><coden>BIPRET</coden><abstract>The effect of cloned gene dosage on growth and product formation under hyperosmotic conditions has been studied using recombinant Chinese hamster ovary (rCHO) cell lines producing chimeric antibody. Batch cultures of four rCHO cell lines carrying different numbers of antibody gene copies were carried out using the hyperosmolar medium. Depending on cloned gene dosage, hyperosmotic pressure decreased specific growth rate (μ) and increased specific antibody productivity (qAb) to a different degree. The cell line with lower cloned gene dosage displayed more significant enhancement in qAb and less reduction in μ at hyperosmolalities. However, the cell line with higher cloned gene dosage still yielded higher maximum antibody concentration at hyperosmolality up to 469 mOsm/kg. Northern blot analysis showed a positive relationship between immunoglobulin mRNA level per cell and qAb, indicating that transcriptional regulation was involved in the response of rCHO cells to hyperosmotic pressure. Cell cycle analysis showed that hyperosmotic pressure induced G1‐phase arrest, suggesting that the increase of cell population in G1‐phase may contribute in part to enhanced
qAb at hyperosmolality. Taken together, although the cell line with lower cloned gene dosage displayed more significant enhancement in qAb at hyperosmolality, the factor that determined the maximum antibody concentration in hyperosmotic rCHO cell cultures was almost exclusively the gene dosage.</abstract><cop>USA</cop><pub>American Chemical Society</pub><pmid>11735431</pmid><doi>10.1021/bp010116e</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 8756-7938 |
ispartof | Biotechnology progress, 2001-11, Vol.17 (6), p.993-999 |
issn | 8756-7938 1520-6033 |
language | eng |
recordid | cdi_proquest_miscellaneous_72336875 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Animals Antibody Formation - physiology Biological and medical sciences Biotechnology Blotting, Northern Cell Cycle Cell Division - physiology CHO Cells - cytology CHO Cells - metabolism Cloning, Molecular Cricetinae Culture Media DNA - biosynthesis Fundamental and applied biological sciences. Psychology Gene Dosage Glucose - metabolism Health. Pharmaceutical industry Industrial applications and implications. Economical aspects Lactic Acid - metabolism Monoclonal antibodies Osmotic Pressure Production of active biomolecules Recombinant Proteins - biosynthesis Recombinant Proteins - genetics RNA, Messenger - biosynthesis Tissue Engineering |
title | Effects of Cloned Gene Dosage on the Response of Recombinant CHO Cells to Hyperosmotic Pressure in Regard to Cell Growth and Antibody Production |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T11%3A18%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Effects%20of%20Cloned%20Gene%20Dosage%20on%20the%20Response%20of%20Recombinant%20CHO%20Cells%20to%20Hyperosmotic%20Pressure%20in%20Regard%20to%20Cell%20Growth%20and%20Antibody%20Production&rft.jtitle=Biotechnology%20progress&rft.au=Ryu,%20Joon%20Soo&rft.date=2001-11-01&rft.volume=17&rft.issue=6&rft.spage=993&rft.epage=999&rft.pages=993-999&rft.issn=8756-7938&rft.eissn=1520-6033&rft.coden=BIPRET&rft_id=info:doi/10.1021/bp010116e&rft_dat=%3Cproquest_cross%3E18367857%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=18367857&rft_id=info:pmid/11735431&rfr_iscdi=true |