Efficient expansion of clinical-grade human fibroblasts on microcarriers: Cells suitable for ex vivo expansion of clinical-grade hESCs
Human embryonic stem cells hold considerable potential for cell-based treatments of a variety of degenerative diseases, including diabetes, ischemic heart failure, and Parkinson's disease. However, advancing research to provide clinical-grade product requires scale-up to therapeutic quantities...
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Veröffentlicht in: | Journal of biotechnology 2008-03, Vol.134 (1), p.79-87 |
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creator | Phillips, Blaine Wesley Lim, Ricky Yee Meng Tan, Thong Teck Rust, William Lathrop Crook, Jeremy Micah |
description | Human embryonic stem cells hold considerable potential for cell-based treatments of a variety of degenerative diseases, including diabetes, ischemic heart failure, and Parkinson's disease. However, advancing research to provide clinical-grade product requires scale-up to therapeutic quantities of stem cells and their differentiated progeny. Most human embryonic stem cell culture platforms require direct support by a fibroblast feeder layer or indirect support using fibroblast conditioned medium. Accordingly, large numbers of clinically compliant fibroblasts will be requisite for stem cell production. Published platforms for feeder production are insufficient for stem cell scale-up, being costly to operate and requiring considerable effort to prepare, maintain and harvest. Here we describe the expansion of cGMP-grade, FDA-approved human foreskin fibroblasts using cGMP-grade reagents and polystyrene-based cationic trimethyl ammonium-coated microcarriers in spinner flasks. Fibroblasts attach rapidly to the microcarriers (
T
1/2
=75
min), and expand with a maximum doubling time of 22.5
h. Importantly, microcarrier-expanded fibroblasts and their conditioned medium support pluripotent stem cell growth through >5 passages, enabling extended self-renewal and expansion while retaining full differentiation potential. In summary, the method described is an economical and cGMP-compliant means of producing human fibroblast cells in support of cGMP human embryonic stem cell culture. |
doi_str_mv | 10.1016/j.jbiotec.2007.12.007 |
format | Article |
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T
1/2
=75
min), and expand with a maximum doubling time of 22.5
h. Importantly, microcarrier-expanded fibroblasts and their conditioned medium support pluripotent stem cell growth through >5 passages, enabling extended self-renewal and expansion while retaining full differentiation potential. In summary, the method described is an economical and cGMP-compliant means of producing human fibroblast cells in support of cGMP human embryonic stem cell culture.</description><identifier>ISSN: 0168-1656</identifier><identifier>EISSN: 1873-4863</identifier><identifier>DOI: 10.1016/j.jbiotec.2007.12.007</identifier><identifier>PMID: 18261818</identifier><identifier>CODEN: JBITD4</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Biological and medical sciences ; Biotechnology ; Cell Culture Techniques - methods ; Cells, Cultured ; Embryonic Stem Cells - cytology ; Embryonic Stem Cells - metabolism ; ES cells ; Fibroblasts - cytology ; Fibroblasts - metabolism ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; Human embryonic stem cells ; Humans ; Immunohistochemistry ; Microcarriers ; Reverse Transcriptase Polymerase Chain Reaction ; Scale-up</subject><ispartof>Journal of biotechnology, 2008-03, Vol.134 (1), p.79-87</ispartof><rights>2007 Elsevier B.V.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-8312b550efc02fa299c457a03a5679ba25a24e9bb7ff573dcc7e07c515c547db3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168165607017956$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20167468$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18261818$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Phillips, Blaine Wesley</creatorcontrib><creatorcontrib>Lim, Ricky Yee Meng</creatorcontrib><creatorcontrib>Tan, Thong Teck</creatorcontrib><creatorcontrib>Rust, William Lathrop</creatorcontrib><creatorcontrib>Crook, Jeremy Micah</creatorcontrib><title>Efficient expansion of clinical-grade human fibroblasts on microcarriers: Cells suitable for ex vivo expansion of clinical-grade hESCs</title><title>Journal of biotechnology</title><addtitle>J Biotechnol</addtitle><description>Human embryonic stem cells hold considerable potential for cell-based treatments of a variety of degenerative diseases, including diabetes, ischemic heart failure, and Parkinson's disease. However, advancing research to provide clinical-grade product requires scale-up to therapeutic quantities of stem cells and their differentiated progeny. Most human embryonic stem cell culture platforms require direct support by a fibroblast feeder layer or indirect support using fibroblast conditioned medium. Accordingly, large numbers of clinically compliant fibroblasts will be requisite for stem cell production. Published platforms for feeder production are insufficient for stem cell scale-up, being costly to operate and requiring considerable effort to prepare, maintain and harvest. Here we describe the expansion of cGMP-grade, FDA-approved human foreskin fibroblasts using cGMP-grade reagents and polystyrene-based cationic trimethyl ammonium-coated microcarriers in spinner flasks. Fibroblasts attach rapidly to the microcarriers (
T
1/2
=75
min), and expand with a maximum doubling time of 22.5
h. Importantly, microcarrier-expanded fibroblasts and their conditioned medium support pluripotent stem cell growth through >5 passages, enabling extended self-renewal and expansion while retaining full differentiation potential. In summary, the method described is an economical and cGMP-compliant means of producing human fibroblast cells in support of cGMP human embryonic stem cell culture.</description><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell Culture Techniques - methods</subject><subject>Cells, Cultured</subject><subject>Embryonic Stem Cells - cytology</subject><subject>Embryonic Stem Cells - metabolism</subject><subject>ES cells</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - metabolism</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Human embryonic stem cells</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Microcarriers</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Scale-up</subject><issn>0168-1656</issn><issn>1873-4863</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksFu1DAURS0EotPCJwDe0F2C7dhxwqZCoykgVWJRuraeHbt4lMSDnYzKD_S762gi2NHVXfi86-d7jdA7SkpKaP1pX-61D5M1JSNElpSVWV6gDW1kVfCmrl6iTeaagtaiPkPnKe0JIbwV9DU6ow2raUObDXrcOeeNt-OE7cMBxuTDiIPDpvejN9AX9xE6i3_NA4zYeR2D7iFNCWds8CYGAzF6G9NnvLV9n3Ca_QS6t9iFmC3x0R_D_613t9v0Br1y0Cf7dtULdHe9-7n9Vtz8-Pp9--WmMJw3U9FUlGkhiHWGMAesbQ0XEkgFopatBiaAcdtqLZ0TsuqMkZZII6gwgstOVxfo8uR7iOH3bNOkBp9MXhxGG-akJKkEoVX7LMiIkDlwnkFxAnMWKUXr1CH6AeIfRYlamlJ7tTallqYUZSpLnnu_XjDrwXb_ptZqMvBxBSDltFyE0fj0l2PZWvJ64T6cOAdBwX3MzN1tPq0IyV-B18tbrk6Ezckec1kqLY0b2_lozaS64J9Z9gnx5b9a</recordid><startdate>20080320</startdate><enddate>20080320</enddate><creator>Phillips, Blaine Wesley</creator><creator>Lim, Ricky Yee Meng</creator><creator>Tan, Thong Teck</creator><creator>Rust, William Lathrop</creator><creator>Crook, Jeremy Micah</creator><general>Elsevier B.V</general><general>[New York, NY]: Elsevier</general><general>Elsevier</general><scope>FBQ</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>20080320</creationdate><title>Efficient expansion of clinical-grade human fibroblasts on microcarriers: Cells suitable for ex vivo expansion of clinical-grade hESCs</title><author>Phillips, Blaine Wesley ; Lim, Ricky Yee Meng ; Tan, Thong Teck ; Rust, William Lathrop ; Crook, Jeremy Micah</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-8312b550efc02fa299c457a03a5679ba25a24e9bb7ff573dcc7e07c515c547db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell Culture Techniques - methods</topic><topic>Cells, Cultured</topic><topic>Embryonic Stem Cells - cytology</topic><topic>Embryonic Stem Cells - metabolism</topic><topic>ES cells</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - metabolism</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Human embryonic stem cells</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Microcarriers</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Scale-up</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Phillips, Blaine Wesley</creatorcontrib><creatorcontrib>Lim, Ricky Yee Meng</creatorcontrib><creatorcontrib>Tan, Thong Teck</creatorcontrib><creatorcontrib>Rust, William Lathrop</creatorcontrib><creatorcontrib>Crook, Jeremy Micah</creatorcontrib><collection>AGRIS</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>Journal of biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Phillips, Blaine Wesley</au><au>Lim, Ricky Yee Meng</au><au>Tan, Thong Teck</au><au>Rust, William Lathrop</au><au>Crook, Jeremy Micah</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient expansion of clinical-grade human fibroblasts on microcarriers: Cells suitable for ex vivo expansion of clinical-grade hESCs</atitle><jtitle>Journal of biotechnology</jtitle><addtitle>J Biotechnol</addtitle><date>2008-03-20</date><risdate>2008</risdate><volume>134</volume><issue>1</issue><spage>79</spage><epage>87</epage><pages>79-87</pages><issn>0168-1656</issn><eissn>1873-4863</eissn><coden>JBITD4</coden><abstract>Human embryonic stem cells hold considerable potential for cell-based treatments of a variety of degenerative diseases, including diabetes, ischemic heart failure, and Parkinson's disease. 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T
1/2
=75
min), and expand with a maximum doubling time of 22.5
h. Importantly, microcarrier-expanded fibroblasts and their conditioned medium support pluripotent stem cell growth through >5 passages, enabling extended self-renewal and expansion while retaining full differentiation potential. In summary, the method described is an economical and cGMP-compliant means of producing human fibroblast cells in support of cGMP human embryonic stem cell culture.</abstract><cop>Lausanne</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>18261818</pmid><doi>10.1016/j.jbiotec.2007.12.007</doi><tpages>9</tpages></addata></record> |
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subjects | Biological and medical sciences Biotechnology Cell Culture Techniques - methods Cells, Cultured Embryonic Stem Cells - cytology Embryonic Stem Cells - metabolism ES cells Fibroblasts - cytology Fibroblasts - metabolism Flow Cytometry Fundamental and applied biological sciences. Psychology Human embryonic stem cells Humans Immunohistochemistry Microcarriers Reverse Transcriptase Polymerase Chain Reaction Scale-up |
title | Efficient expansion of clinical-grade human fibroblasts on microcarriers: Cells suitable for ex vivo expansion of clinical-grade hESCs |
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