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Modularized dynamic cell culture platform for efficient production of extracellular vesicles and sequential analysis
Extracellular vesicles (EVs) are nanometer-sized particles naturally secreted by cells for intercellular communication that encapsulate bioactive cargo, such as proteins and RNA, with a lipid bilayer. Tumor cell-derived EVs (tdEVs) are particularly promising biomarkers for cancer research because th...
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Published in: | Lab on a chip 2023-03, Vol.23 (7), p.1852-1864 |
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container_title | Lab on a chip |
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creator | Kim, Seo Yeon Ha, Seong Min Kim, Dong-Uk Park, Junhyun Park, Sunyoung Hyun, Kyung-A Jung, Hyo-Il |
description | Extracellular vesicles (EVs) are nanometer-sized particles naturally secreted by cells for intercellular communication that encapsulate bioactive cargo, such as proteins and RNA, with a lipid bilayer. Tumor cell-derived EVs (tdEVs) are particularly promising biomarkers for cancer research because their contents reflect the cell of origin. In most studies, tdEVs have been obtained from cancer cells cultured under static conditions, thus lacking the ability to recapitulate the microenvironment of cells
in vivo
. Recent developments in perfusable cell culture systems have allowed oxygen and a nutrient gradient to mimic the physiological and cellular microenvironment. However, as these systems are perfused by circulating the culture medium within the unified structure, independently harvesting cells and EVs at each time point for analysis presents a limitation. In this study, a modularized cell culture system is designed for the perfusion and real-time collection of EVs. The system consists of three detachable chambers, one each for fresh medium, cell culture, and EV collection. The fresh medium flows from the medium chamber to the culture chamber at a flow rate controlled by the hydraulic pressure injected with a syringe pump. When the culture medium containing EVs exceeds a certain volume within the chamber, it overflows into the collection chamber to harvest EVs. The compact and modularized chambers are highly interoperable with conventional cell culture modalities used in the laboratory, thus enabling various EV-based assays.
A modularized system is designed to replicate cellular environment and sequentially harvest extracellular vesicles released from cells. The system allows long-term culture under interstitial flow and simple metabolite collection
via
modularization. |
doi_str_mv | 10.1039/d2lc01129h |
format | article |
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in vivo
. Recent developments in perfusable cell culture systems have allowed oxygen and a nutrient gradient to mimic the physiological and cellular microenvironment. However, as these systems are perfused by circulating the culture medium within the unified structure, independently harvesting cells and EVs at each time point for analysis presents a limitation. In this study, a modularized cell culture system is designed for the perfusion and real-time collection of EVs. The system consists of three detachable chambers, one each for fresh medium, cell culture, and EV collection. The fresh medium flows from the medium chamber to the culture chamber at a flow rate controlled by the hydraulic pressure injected with a syringe pump. When the culture medium containing EVs exceeds a certain volume within the chamber, it overflows into the collection chamber to harvest EVs. The compact and modularized chambers are highly interoperable with conventional cell culture modalities used in the laboratory, thus enabling various EV-based assays.
A modularized system is designed to replicate cellular environment and sequentially harvest extracellular vesicles released from cells. The system allows long-term culture under interstitial flow and simple metabolite collection
via
modularization.</description><identifier>ISSN: 1473-0197</identifier><identifier>EISSN: 1473-0189</identifier><identifier>DOI: 10.1039/d2lc01129h</identifier><identifier>PMID: 36825402</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Biomarkers ; Biomarkers - metabolism ; Cancer ; Cell culture ; Cell Culture Techniques ; Chambers ; Collection ; Extracellular vesicles ; Extracellular Vesicles - metabolism ; Flow velocity ; Hydraulic pressure ; Lipids ; Perfusion ; Sequential analysis ; Vesicles</subject><ispartof>Lab on a chip, 2023-03, Vol.23 (7), p.1852-1864</ispartof><rights>Copyright Royal Society of Chemistry 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c337t-53e31bec999b213e3ab125011dcbb296dd03d5fab1f361fcfb3f617fc3c4dafc3</citedby><cites>FETCH-LOGICAL-c337t-53e31bec999b213e3ab125011dcbb296dd03d5fab1f361fcfb3f617fc3c4dafc3</cites><orcidid>0000-0003-1923-9997 ; 0000-0002-7474-9378</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36825402$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Seo Yeon</creatorcontrib><creatorcontrib>Ha, Seong Min</creatorcontrib><creatorcontrib>Kim, Dong-Uk</creatorcontrib><creatorcontrib>Park, Junhyun</creatorcontrib><creatorcontrib>Park, Sunyoung</creatorcontrib><creatorcontrib>Hyun, Kyung-A</creatorcontrib><creatorcontrib>Jung, Hyo-Il</creatorcontrib><title>Modularized dynamic cell culture platform for efficient production of extracellular vesicles and sequential analysis</title><title>Lab on a chip</title><addtitle>Lab Chip</addtitle><description>Extracellular vesicles (EVs) are nanometer-sized particles naturally secreted by cells for intercellular communication that encapsulate bioactive cargo, such as proteins and RNA, with a lipid bilayer. Tumor cell-derived EVs (tdEVs) are particularly promising biomarkers for cancer research because their contents reflect the cell of origin. In most studies, tdEVs have been obtained from cancer cells cultured under static conditions, thus lacking the ability to recapitulate the microenvironment of cells
in vivo
. Recent developments in perfusable cell culture systems have allowed oxygen and a nutrient gradient to mimic the physiological and cellular microenvironment. However, as these systems are perfused by circulating the culture medium within the unified structure, independently harvesting cells and EVs at each time point for analysis presents a limitation. In this study, a modularized cell culture system is designed for the perfusion and real-time collection of EVs. The system consists of three detachable chambers, one each for fresh medium, cell culture, and EV collection. The fresh medium flows from the medium chamber to the culture chamber at a flow rate controlled by the hydraulic pressure injected with a syringe pump. When the culture medium containing EVs exceeds a certain volume within the chamber, it overflows into the collection chamber to harvest EVs. The compact and modularized chambers are highly interoperable with conventional cell culture modalities used in the laboratory, thus enabling various EV-based assays.
A modularized system is designed to replicate cellular environment and sequentially harvest extracellular vesicles released from cells. The system allows long-term culture under interstitial flow and simple metabolite collection
via
modularization.</description><subject>Biomarkers</subject><subject>Biomarkers - metabolism</subject><subject>Cancer</subject><subject>Cell culture</subject><subject>Cell Culture Techniques</subject><subject>Chambers</subject><subject>Collection</subject><subject>Extracellular vesicles</subject><subject>Extracellular Vesicles - metabolism</subject><subject>Flow velocity</subject><subject>Hydraulic pressure</subject><subject>Lipids</subject><subject>Perfusion</subject><subject>Sequential analysis</subject><subject>Vesicles</subject><issn>1473-0197</issn><issn>1473-0189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpdkUtLAzEUhYMoVqsb90rAjQjVPOaVpdRHhYobXQ-ZPDAlM1OTGbH-eu_YWsFNbm7yncNJLkInlFxRwsW1Zl4RSpl420EHNMn5hNBC7G73Ih-hwxgXhNA0yYp9NOJZwdKEsAPUPbW69zK4L6OxXjWydgor4z1Wve_6YPDSy862ocawYGOtU840HV4GEKrOtQ1uLTafXZCDbPDCHyY65U3EstE4mvceBE56aKVfRReP0J6VPprjTR2j1_u7l-lsMn9-eJzezCeK87ybpNxwWhklhKgYhUZWlKXwUq2qiolMa8J1auHU8oxaZStuM5pbxVWiJZQxulj7QlgIEbuydnFIKRvT9rFkeUFIJjjlgJ7_QxdtHyDvQAmakRxgoC7XlAptjMHYchlcLcOqpKQcZlHesvn0ZxYzgM82ln1VG71Ffz8fgNM1EKLa3v4Nk38D_fiRHA</recordid><startdate>20230328</startdate><enddate>20230328</enddate><creator>Kim, Seo Yeon</creator><creator>Ha, Seong Min</creator><creator>Kim, Dong-Uk</creator><creator>Park, Junhyun</creator><creator>Park, Sunyoung</creator><creator>Hyun, Kyung-A</creator><creator>Jung, Hyo-Il</creator><general>Royal Society of Chemistry</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>7SP</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1923-9997</orcidid><orcidid>https://orcid.org/0000-0002-7474-9378</orcidid></search><sort><creationdate>20230328</creationdate><title>Modularized dynamic cell culture platform for efficient production of extracellular vesicles and sequential analysis</title><author>Kim, Seo Yeon ; Ha, Seong Min ; Kim, Dong-Uk ; Park, Junhyun ; Park, Sunyoung ; Hyun, Kyung-A ; Jung, Hyo-Il</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-53e31bec999b213e3ab125011dcbb296dd03d5fab1f361fcfb3f617fc3c4dafc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biomarkers</topic><topic>Biomarkers - metabolism</topic><topic>Cancer</topic><topic>Cell culture</topic><topic>Cell Culture Techniques</topic><topic>Chambers</topic><topic>Collection</topic><topic>Extracellular vesicles</topic><topic>Extracellular Vesicles - metabolism</topic><topic>Flow velocity</topic><topic>Hydraulic pressure</topic><topic>Lipids</topic><topic>Perfusion</topic><topic>Sequential analysis</topic><topic>Vesicles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Seo Yeon</creatorcontrib><creatorcontrib>Ha, Seong Min</creatorcontrib><creatorcontrib>Kim, Dong-Uk</creatorcontrib><creatorcontrib>Park, Junhyun</creatorcontrib><creatorcontrib>Park, Sunyoung</creatorcontrib><creatorcontrib>Hyun, Kyung-A</creatorcontrib><creatorcontrib>Jung, Hyo-Il</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Lab on a chip</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Seo Yeon</au><au>Ha, Seong Min</au><au>Kim, Dong-Uk</au><au>Park, Junhyun</au><au>Park, Sunyoung</au><au>Hyun, Kyung-A</au><au>Jung, Hyo-Il</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modularized dynamic cell culture platform for efficient production of extracellular vesicles and sequential analysis</atitle><jtitle>Lab on a chip</jtitle><addtitle>Lab Chip</addtitle><date>2023-03-28</date><risdate>2023</risdate><volume>23</volume><issue>7</issue><spage>1852</spage><epage>1864</epage><pages>1852-1864</pages><issn>1473-0197</issn><eissn>1473-0189</eissn><abstract>Extracellular vesicles (EVs) are nanometer-sized particles naturally secreted by cells for intercellular communication that encapsulate bioactive cargo, such as proteins and RNA, with a lipid bilayer. Tumor cell-derived EVs (tdEVs) are particularly promising biomarkers for cancer research because their contents reflect the cell of origin. In most studies, tdEVs have been obtained from cancer cells cultured under static conditions, thus lacking the ability to recapitulate the microenvironment of cells
in vivo
. Recent developments in perfusable cell culture systems have allowed oxygen and a nutrient gradient to mimic the physiological and cellular microenvironment. However, as these systems are perfused by circulating the culture medium within the unified structure, independently harvesting cells and EVs at each time point for analysis presents a limitation. In this study, a modularized cell culture system is designed for the perfusion and real-time collection of EVs. The system consists of three detachable chambers, one each for fresh medium, cell culture, and EV collection. The fresh medium flows from the medium chamber to the culture chamber at a flow rate controlled by the hydraulic pressure injected with a syringe pump. When the culture medium containing EVs exceeds a certain volume within the chamber, it overflows into the collection chamber to harvest EVs. The compact and modularized chambers are highly interoperable with conventional cell culture modalities used in the laboratory, thus enabling various EV-based assays.
A modularized system is designed to replicate cellular environment and sequentially harvest extracellular vesicles released from cells. The system allows long-term culture under interstitial flow and simple metabolite collection
via
modularization.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>36825402</pmid><doi>10.1039/d2lc01129h</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-1923-9997</orcidid><orcidid>https://orcid.org/0000-0002-7474-9378</orcidid></addata></record> |
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subjects | Biomarkers Biomarkers - metabolism Cancer Cell culture Cell Culture Techniques Chambers Collection Extracellular vesicles Extracellular Vesicles - metabolism Flow velocity Hydraulic pressure Lipids Perfusion Sequential analysis Vesicles |
title | Modularized dynamic cell culture platform for efficient production of extracellular vesicles and sequential analysis |
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