An automatic cell culture platform for differentiation of human induced pluripotent stem cells
We developed an automatic cell culture platform to facilitate the research and development of stem cell differentiation. This platform consists of a distributor of culture media containing different cell factors, a culture unit allowing either static or dynamic exchange of the medium and a central u...
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Veröffentlicht in: | Microelectronic engineering 2020-07, Vol.231, p.111371, Article 111371 |
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creator | Pitingolo, Gabriele He, Yong Huang, Boxin Wang, Li Shi, Jian Chen, Yong |
description | We developed an automatic cell culture platform to facilitate the research and development of stem cell differentiation. This platform consists of a distributor of culture media containing different cell factors, a culture unit allowing either static or dynamic exchange of the medium and a central unit for pumping and process control, respectively. This platform was firstly used for cell culture with a tissue culture dish at a high medium exchange rate, showing an increased cell growth due to enhanced uptake of the nutrients and enhanced clearance of the metabolites. Then, the platform was used for automatic differentiation of human induced pluripotent stem cells (hiPSCs) toward cardiomyocytes which involved six types of culture media. As results, functional cardiomyocytes could be obtained after automatic processing during two weeks, showing regular beating over a large area. Details are described to promote the application of the platform to other types of stem cell differentiation or cell-based assays.
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•Development of a laboratory platform for automatic differentiation of stem cells.•Demonstration of automatic cell culture with either static or dynamic medium renewal.•Demonstration of automated cardiac differentiation of human induced pluripotent stem cells. |
doi_str_mv | 10.1016/j.mee.2020.111371 |
format | Article |
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•Development of a laboratory platform for automatic differentiation of stem cells.•Demonstration of automatic cell culture with either static or dynamic medium renewal.•Demonstration of automated cardiac differentiation of human induced pluripotent stem cells.</description><identifier>ISSN: 0167-9317</identifier><identifier>EISSN: 1873-5568</identifier><identifier>DOI: 10.1016/j.mee.2020.111371</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Automation ; Biotechnology ; Cardiomyocytes ; Cell culture ; Cell growth ; Differentiation (biology) ; Distributors ; Life Sciences ; Metabolites ; Nutrients ; Process controls ; R&D ; Research & development ; Stem cell differentiation ; Stem cells ; Tissue engineering</subject><ispartof>Microelectronic engineering, 2020-07, Vol.231, p.111371, Article 111371</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright Elsevier BV Jul 15, 2020</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-6e6d27b662a1e6ebf610f540650ab46522822685856e1691bbaff99e3c0ba8953</citedby><cites>FETCH-LOGICAL-c402t-6e6d27b662a1e6ebf610f540650ab46522822685856e1691bbaff99e3c0ba8953</cites><orcidid>0000-0002-2903-8753 ; 0000-0002-4232-3348 ; 0000-0002-1969-7579</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mee.2020.111371$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://hal.science/hal-03013336$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Pitingolo, Gabriele</creatorcontrib><creatorcontrib>He, Yong</creatorcontrib><creatorcontrib>Huang, Boxin</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Shi, Jian</creatorcontrib><creatorcontrib>Chen, Yong</creatorcontrib><title>An automatic cell culture platform for differentiation of human induced pluripotent stem cells</title><title>Microelectronic engineering</title><description>We developed an automatic cell culture platform to facilitate the research and development of stem cell differentiation. This platform consists of a distributor of culture media containing different cell factors, a culture unit allowing either static or dynamic exchange of the medium and a central unit for pumping and process control, respectively. This platform was firstly used for cell culture with a tissue culture dish at a high medium exchange rate, showing an increased cell growth due to enhanced uptake of the nutrients and enhanced clearance of the metabolites. Then, the platform was used for automatic differentiation of human induced pluripotent stem cells (hiPSCs) toward cardiomyocytes which involved six types of culture media. As results, functional cardiomyocytes could be obtained after automatic processing during two weeks, showing regular beating over a large area. Details are described to promote the application of the platform to other types of stem cell differentiation or cell-based assays.
[Display omitted]
•Development of a laboratory platform for automatic differentiation of stem cells.•Demonstration of automatic cell culture with either static or dynamic medium renewal.•Demonstration of automated cardiac differentiation of human induced pluripotent stem cells.</description><subject>Automation</subject><subject>Biotechnology</subject><subject>Cardiomyocytes</subject><subject>Cell culture</subject><subject>Cell growth</subject><subject>Differentiation (biology)</subject><subject>Distributors</subject><subject>Life Sciences</subject><subject>Metabolites</subject><subject>Nutrients</subject><subject>Process controls</subject><subject>R&D</subject><subject>Research & development</subject><subject>Stem cell differentiation</subject><subject>Stem cells</subject><subject>Tissue engineering</subject><issn>0167-9317</issn><issn>1873-5568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kMtKxDAUhoMoOF4ewF3AlYuOuTRpi6th8AYDbnRrSNMTzNA2Y5IO-PZmrLh0k3DC9_-cfAhdUbKkhMrb7XIAWDLC8kwpr-gRWtC64oUQsj5Gi8xURcNpdYrOYtySPJekXqD31Yj1lPygkzPYQN9jM_VpCoB3vU7WhwHnA3fOWggwJpdBP2Jv8cc06BG7sZsMdJmegtv5lBEcEww_XfECnVjdR7j8vc_R28P96_qp2Lw8Pq9Xm8KUhKVCguxY1UrJNAUJrZWUWFESKYhuSykYqxmTtaiFBCob2rba2qYBbkir60bwc3Qz937oXu2CG3T4Ul479bTaqMMb4YRyzuWeZvZ6ZnfBf04Qk9r6KYx5PcXKshJVXqPKFJ0pE3yMAexfLSXqoFxtVVauDsrVrDxn7uYM5K_uHQQVjYMx63EBTFKdd_-kvwF964hq</recordid><startdate>20200715</startdate><enddate>20200715</enddate><creator>Pitingolo, Gabriele</creator><creator>He, Yong</creator><creator>Huang, Boxin</creator><creator>Wang, Li</creator><creator>Shi, Jian</creator><creator>Chen, Yong</creator><general>Elsevier B.V</general><general>Elsevier BV</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>8FD</scope><scope>L7M</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0002-2903-8753</orcidid><orcidid>https://orcid.org/0000-0002-4232-3348</orcidid><orcidid>https://orcid.org/0000-0002-1969-7579</orcidid></search><sort><creationdate>20200715</creationdate><title>An automatic cell culture platform for differentiation of human induced pluripotent stem cells</title><author>Pitingolo, Gabriele ; He, Yong ; Huang, Boxin ; Wang, Li ; Shi, Jian ; Chen, Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-6e6d27b662a1e6ebf610f540650ab46522822685856e1691bbaff99e3c0ba8953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Automation</topic><topic>Biotechnology</topic><topic>Cardiomyocytes</topic><topic>Cell culture</topic><topic>Cell growth</topic><topic>Differentiation (biology)</topic><topic>Distributors</topic><topic>Life Sciences</topic><topic>Metabolites</topic><topic>Nutrients</topic><topic>Process controls</topic><topic>R&D</topic><topic>Research & development</topic><topic>Stem cell differentiation</topic><topic>Stem cells</topic><topic>Tissue engineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pitingolo, Gabriele</creatorcontrib><creatorcontrib>He, Yong</creatorcontrib><creatorcontrib>Huang, Boxin</creatorcontrib><creatorcontrib>Wang, Li</creatorcontrib><creatorcontrib>Shi, Jian</creatorcontrib><creatorcontrib>Chen, Yong</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Microelectronic engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pitingolo, Gabriele</au><au>He, Yong</au><au>Huang, Boxin</au><au>Wang, Li</au><au>Shi, Jian</au><au>Chen, Yong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An automatic cell culture platform for differentiation of human induced pluripotent stem cells</atitle><jtitle>Microelectronic engineering</jtitle><date>2020-07-15</date><risdate>2020</risdate><volume>231</volume><spage>111371</spage><pages>111371-</pages><artnum>111371</artnum><issn>0167-9317</issn><eissn>1873-5568</eissn><abstract>We developed an automatic cell culture platform to facilitate the research and development of stem cell differentiation. This platform consists of a distributor of culture media containing different cell factors, a culture unit allowing either static or dynamic exchange of the medium and a central unit for pumping and process control, respectively. This platform was firstly used for cell culture with a tissue culture dish at a high medium exchange rate, showing an increased cell growth due to enhanced uptake of the nutrients and enhanced clearance of the metabolites. Then, the platform was used for automatic differentiation of human induced pluripotent stem cells (hiPSCs) toward cardiomyocytes which involved six types of culture media. As results, functional cardiomyocytes could be obtained after automatic processing during two weeks, showing regular beating over a large area. Details are described to promote the application of the platform to other types of stem cell differentiation or cell-based assays.
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•Development of a laboratory platform for automatic differentiation of stem cells.•Demonstration of automatic cell culture with either static or dynamic medium renewal.•Demonstration of automated cardiac differentiation of human induced pluripotent stem cells.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.mee.2020.111371</doi><orcidid>https://orcid.org/0000-0002-2903-8753</orcidid><orcidid>https://orcid.org/0000-0002-4232-3348</orcidid><orcidid>https://orcid.org/0000-0002-1969-7579</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Automation Biotechnology Cardiomyocytes Cell culture Cell growth Differentiation (biology) Distributors Life Sciences Metabolites Nutrients Process controls R&D Research & development Stem cell differentiation Stem cells Tissue engineering |
title | An automatic cell culture platform for differentiation of human induced pluripotent stem cells |
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