Extended serial passaging of mammalian neural stem cells in suspension bioreactors
Neural stem cells (NSCs) are primitive cells that are the “parent” cells of all the cells in the central nervous system (CNS). Their discovery in 1992 opened the door to a multitude of potential therapies and treatments to cure neurodegenerative diseases such as Parkinson's disease, multiple sc...
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Veröffentlicht in: | Biotechnology and bioengineering 1999-12, Vol.65 (5), p.589-599 |
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creator | Kallos, Michael S. Behie, Leo A. Vescovi, Angelo L. |
description | Neural stem cells (NSCs) are primitive cells that are the “parent” cells of all the cells in the central nervous system (CNS). Their discovery in 1992 opened the door to a multitude of potential therapies and treatments to cure neurodegenerative diseases such as Parkinson's disease, multiple sclerosis, and Huntington's disease, which affect millions of people worldwide and cost billions of dollars in health care each year. This study proposes optimal serial passaging protocols so that mammalian neural stem cells can effectively be grown in suspension culture. We examined stationary culture passaging protocols and developed our own optimal procedure. Also examined was the effect of serially cultivating the neural stem cells in suspension culture for an extended period of time. The cells were grown for over 35 days in suspension with an overall multiplication ratio of over 107 with no decrease in growth rate, maximum cell density, or viability. The cells also remained karyotypically normal through 25 doublings and retained their ability to be differentiated into all the major cell types of the CNS—neurons, astrocytes, and oligodendrocytes. For the first time, mammalian neural stem cells were grown on a larger scale in suspension culture and maintained their stem cell characteristics. A semicontinuous scheme for large‐scale production is also presented. © 1999 John Wiley & Sons, Inc. Biotechnol Bioeng 65: 589–599, 1999. |
doi_str_mv | 10.1002/(SICI)1097-0290(19991205)65:5<589::AID-BIT12>3.0.CO;2-S |
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Their discovery in 1992 opened the door to a multitude of potential therapies and treatments to cure neurodegenerative diseases such as Parkinson's disease, multiple sclerosis, and Huntington's disease, which affect millions of people worldwide and cost billions of dollars in health care each year. This study proposes optimal serial passaging protocols so that mammalian neural stem cells can effectively be grown in suspension culture. We examined stationary culture passaging protocols and developed our own optimal procedure. Also examined was the effect of serially cultivating the neural stem cells in suspension culture for an extended period of time. The cells were grown for over 35 days in suspension with an overall multiplication ratio of over 107 with no decrease in growth rate, maximum cell density, or viability. The cells also remained karyotypically normal through 25 doublings and retained their ability to be differentiated into all the major cell types of the CNS—neurons, astrocytes, and oligodendrocytes. For the first time, mammalian neural stem cells were grown on a larger scale in suspension culture and maintained their stem cell characteristics. A semicontinuous scheme for large‐scale production is also presented. © 1999 John Wiley & Sons, Inc. Biotechnol Bioeng 65: 589–599, 1999.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/(SICI)1097-0290(19991205)65:5<589::AID-BIT12>3.0.CO;2-S</identifier><identifier>PMID: 10516585</identifier><identifier>CODEN: BIBIAU</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Agglomeration ; aggregates ; Animal cells ; Animals ; Astrocytes - cytology ; Biological and medical sciences ; Bioreactors ; Biotechnology ; Cell Culture Techniques - methods ; Cell Differentiation ; Cell Division ; Cell Line ; Cell Separation - methods ; Central Nervous System - cytology ; Establishment of new cell lines, improvement of cultural methods, mass cultures ; Eukaryotic cell cultures ; expansion ; extended culture ; Fundamental and applied biological sciences. Psychology ; mammalian neural stem cells ; Methods. Procedures. Technologies ; Mice ; Neurons - cytology ; Oligodendroglia - cytology ; serial passaging ; Stem Cells - cytology ; suspension bioreactor ; Suspensions (fluids)</subject><ispartof>Biotechnology and bioengineering, 1999-12, Vol.65 (5), p.589-599</ispartof><rights>Copyright © 1999 John Wiley & Sons, Inc.</rights><rights>1999 INIST-CNRS</rights><rights>Copyright 1999 John Wiley & Sons, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c5352-457989707f450d7ccc94eda4870f41e5d590cfe09d8287b9d1452a409d2798e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291097-0290%2819991205%2965%3A5%3C589%3A%3AAID-BIT12%3E3.0.CO%3B2-S$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291097-0290%2819991205%2965%3A5%3C589%3A%3AAID-BIT12%3E3.0.CO%3B2-S$$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=1984033$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10516585$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kallos, Michael S.</creatorcontrib><creatorcontrib>Behie, Leo A.</creatorcontrib><creatorcontrib>Vescovi, Angelo L.</creatorcontrib><title>Extended serial passaging of mammalian neural stem cells in suspension bioreactors</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol. Bioeng</addtitle><description>Neural stem cells (NSCs) are primitive cells that are the “parent” cells of all the cells in the central nervous system (CNS). Their discovery in 1992 opened the door to a multitude of potential therapies and treatments to cure neurodegenerative diseases such as Parkinson's disease, multiple sclerosis, and Huntington's disease, which affect millions of people worldwide and cost billions of dollars in health care each year. This study proposes optimal serial passaging protocols so that mammalian neural stem cells can effectively be grown in suspension culture. We examined stationary culture passaging protocols and developed our own optimal procedure. Also examined was the effect of serially cultivating the neural stem cells in suspension culture for an extended period of time. The cells were grown for over 35 days in suspension with an overall multiplication ratio of over 107 with no decrease in growth rate, maximum cell density, or viability. The cells also remained karyotypically normal through 25 doublings and retained their ability to be differentiated into all the major cell types of the CNS—neurons, astrocytes, and oligodendrocytes. For the first time, mammalian neural stem cells were grown on a larger scale in suspension culture and maintained their stem cell characteristics. A semicontinuous scheme for large‐scale production is also presented. © 1999 John Wiley & Sons, Inc. Biotechnol Bioeng 65: 589–599, 1999.</description><subject>Agglomeration</subject><subject>aggregates</subject><subject>Animal cells</subject><subject>Animals</subject><subject>Astrocytes - cytology</subject><subject>Biological and medical sciences</subject><subject>Bioreactors</subject><subject>Biotechnology</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell Differentiation</subject><subject>Cell Division</subject><subject>Cell Line</subject><subject>Cell Separation - methods</subject><subject>Central Nervous System - cytology</subject><subject>Establishment of new cell lines, improvement of cultural methods, mass cultures</subject><subject>Eukaryotic cell cultures</subject><subject>expansion</subject><subject>extended culture</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>mammalian neural stem cells</subject><subject>Methods. Procedures. Technologies</subject><subject>Mice</subject><subject>Neurons - cytology</subject><subject>Oligodendroglia - cytology</subject><subject>serial passaging</subject><subject>Stem Cells - cytology</subject><subject>suspension bioreactor</subject><subject>Suspensions (fluids)</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkl1rFDEUhgdRbK3-BZkLkfZi1pOvSbKKUse6XakuuCsVbw7ZmUyJzsea7GL77806axUUllyEJM95eeFJkrwiMCIA9NnxfFpMTwhomQHVcEy01oSCOMnFWLwQSo_Hp9M32evpgtCXbASjYvacZvM7yeHtzN3kEADyjAlND5IHIXyNR6ny_H5yQECQXChxmHw8u17brrJVGqx3pklXJgRz5bqrtK_T1rStaZzp0s5ufHwNa9umpW2akLouDZuwsl1wfZcuXe-tKde9Dw-Te7Vpgn2024-ST2_PFsV5djGbTIvTi6wUTNCMC6mVliBrLqCSZVlqbivDlYSaEysqoaGsLehKUSWXuiJcUMPjmcZBS9lR8nTIXfn--8aGNbYubLuZzvabgBIUE4KpvSAlTHPI94NE8pxLLSN4OYCl70PwtsaVd63xN0gAtwIRtwJxKwO3MvC3QMwFxqU0YhSIvwQiQ8BihhTnMfnxrsJm2drqr9zBWASe7AATStPU3nSlC384rTgwFrHPA_bDNfbmn3p72_2v3HARo7Mh2sXfcH0bbfw3zCWTAi8_TPDdooAv7yfnyNlPQtbRoA</recordid><startdate>19991205</startdate><enddate>19991205</enddate><creator>Kallos, Michael S.</creator><creator>Behie, Leo A.</creator><creator>Vescovi, Angelo L.</creator><general>John Wiley & Sons, Inc</general><general>Wiley</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>19991205</creationdate><title>Extended serial passaging of mammalian neural stem cells in suspension bioreactors</title><author>Kallos, Michael S. ; Behie, Leo A. ; Vescovi, Angelo L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5352-457989707f450d7ccc94eda4870f41e5d590cfe09d8287b9d1452a409d2798e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Agglomeration</topic><topic>aggregates</topic><topic>Animal cells</topic><topic>Animals</topic><topic>Astrocytes - cytology</topic><topic>Biological and medical sciences</topic><topic>Bioreactors</topic><topic>Biotechnology</topic><topic>Cell Culture Techniques - methods</topic><topic>Cell Differentiation</topic><topic>Cell Division</topic><topic>Cell Line</topic><topic>Cell Separation - methods</topic><topic>Central Nervous System - cytology</topic><topic>Establishment of new cell lines, improvement of cultural methods, mass cultures</topic><topic>Eukaryotic cell cultures</topic><topic>expansion</topic><topic>extended culture</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>mammalian neural stem cells</topic><topic>Methods. Procedures. Technologies</topic><topic>Mice</topic><topic>Neurons - cytology</topic><topic>Oligodendroglia - cytology</topic><topic>serial passaging</topic><topic>Stem Cells - cytology</topic><topic>suspension bioreactor</topic><topic>Suspensions (fluids)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kallos, Michael S.</creatorcontrib><creatorcontrib>Behie, Leo A.</creatorcontrib><creatorcontrib>Vescovi, Angelo L.</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 and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kallos, Michael S.</au><au>Behie, Leo A.</au><au>Vescovi, Angelo L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extended serial passaging of mammalian neural stem cells in suspension bioreactors</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>1999-12-05</date><risdate>1999</risdate><volume>65</volume><issue>5</issue><spage>589</spage><epage>599</epage><pages>589-599</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><coden>BIBIAU</coden><abstract>Neural stem cells (NSCs) are primitive cells that are the “parent” cells of all the cells in the central nervous system (CNS). Their discovery in 1992 opened the door to a multitude of potential therapies and treatments to cure neurodegenerative diseases such as Parkinson's disease, multiple sclerosis, and Huntington's disease, which affect millions of people worldwide and cost billions of dollars in health care each year. This study proposes optimal serial passaging protocols so that mammalian neural stem cells can effectively be grown in suspension culture. We examined stationary culture passaging protocols and developed our own optimal procedure. Also examined was the effect of serially cultivating the neural stem cells in suspension culture for an extended period of time. The cells were grown for over 35 days in suspension with an overall multiplication ratio of over 107 with no decrease in growth rate, maximum cell density, or viability. The cells also remained karyotypically normal through 25 doublings and retained their ability to be differentiated into all the major cell types of the CNS—neurons, astrocytes, and oligodendrocytes. For the first time, mammalian neural stem cells were grown on a larger scale in suspension culture and maintained their stem cell characteristics. A semicontinuous scheme for large‐scale production is also presented. © 1999 John Wiley & Sons, Inc. Biotechnol Bioeng 65: 589–599, 1999.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>10516585</pmid><doi>10.1002/(SICI)1097-0290(19991205)65:5<589::AID-BIT12>3.0.CO;2-S</doi><tpages>11</tpages></addata></record> |
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subjects | Agglomeration aggregates Animal cells Animals Astrocytes - cytology Biological and medical sciences Bioreactors Biotechnology Cell Culture Techniques - methods Cell Differentiation Cell Division Cell Line Cell Separation - methods Central Nervous System - cytology Establishment of new cell lines, improvement of cultural methods, mass cultures Eukaryotic cell cultures expansion extended culture Fundamental and applied biological sciences. Psychology mammalian neural stem cells Methods. Procedures. Technologies Mice Neurons - cytology Oligodendroglia - cytology serial passaging Stem Cells - cytology suspension bioreactor Suspensions (fluids) |
title | Extended serial passaging of mammalian neural stem cells in suspension bioreactors |
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