Scalable mesenchymal stem cell enrichment from bone marrow aspirate using deterministic lateral displacement (DLD) microfluidic sorting
The growing interest in regenerative medicine has opened new avenues for novel cell therapies using stem cells. Bone marrow aspirate (BMA) is an important source of stromal mesenchymal stem cells (MSCs). Conventional MSC harvesting from BMA relies on archaic centrifugation methods, often leading to...
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Veröffentlicht in: | Lab on a chip 2023-09, Vol.23 (19), p.4313-4323 |
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creator | Tan Kwan Zen, Nicholas Zeming, Kerwin Kwek Teo, Kim Leng Loberas, Mavis Lee, Jialing Goh, Chin Ren Yang, Da Hou Oh, Steve Hui Hoi Po, James Cool, Simon M Hou, Han Wei Han, Jongyoon |
description | The growing interest in regenerative medicine has opened new avenues for novel cell therapies using stem cells. Bone marrow aspirate (BMA) is an important source of stromal mesenchymal stem cells (MSCs). Conventional MSC harvesting from BMA relies on archaic centrifugation methods, often leading to poor yield due to osmotic stress, high centrifugation force, convoluted workflow, and long experimental time (∼2-3 hours). To address these issues, we have developed a scalable microfluidic technology based on deterministic lateral displacement (DLD) for MSC isolation. This passive, label-free cell sorting method capitalizes on the morphological differences between MSCs and blood cells (platelets and RBCs) for effective separation using an inverted L-shaped pillar array. To improve throughput, we developed a novel multi-chip DLD system that can process 2.5 mL of raw BMA in 20 ± 5 minutes, achieving a 2-fold increase in MSC recovery compared to centrifugation methods. Taken together, we envision that the developed DLD platform will enable fast and efficient isolation of MSCs from BMA for effective downstream cell therapy in clinical settings.
MSCs are enriched twice more efficiently with 10-fold shorten processing time from undiluted human bone marrow aspirate. |
doi_str_mv | 10.1039/d3lc00379e |
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MSCs are enriched twice more efficiently with 10-fold shorten processing time from undiluted human bone marrow aspirate.</description><identifier>ISSN: 1473-0197</identifier><identifier>EISSN: 1473-0189</identifier><identifier>DOI: 10.1039/d3lc00379e</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Blood cells ; Bone marrow ; Lateral displacement ; Microfluidics ; Stem cells ; Workflow</subject><ispartof>Lab on a chip, 2023-09, Vol.23 (19), p.4313-4323</ispartof><rights>Copyright Royal Society of Chemistry 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c350t-b53dfd46170ebc5b7a75c6e1c49307b87a204ed7c76540fcbf6b196bad0b59fc3</citedby><cites>FETCH-LOGICAL-c350t-b53dfd46170ebc5b7a75c6e1c49307b87a204ed7c76540fcbf6b196bad0b59fc3</cites><orcidid>0000-0001-6631-6321 ; 0009-0004-0453-8577 ; 0000-0001-8543-3056 ; 0000-0001-7215-1439 ; 0000-0002-3088-3604</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27926,27927</link.rule.ids></links><search><creatorcontrib>Tan Kwan Zen, Nicholas</creatorcontrib><creatorcontrib>Zeming, Kerwin Kwek</creatorcontrib><creatorcontrib>Teo, Kim Leng</creatorcontrib><creatorcontrib>Loberas, Mavis</creatorcontrib><creatorcontrib>Lee, Jialing</creatorcontrib><creatorcontrib>Goh, Chin Ren</creatorcontrib><creatorcontrib>Yang, Da Hou</creatorcontrib><creatorcontrib>Oh, Steve</creatorcontrib><creatorcontrib>Hui Hoi Po, James</creatorcontrib><creatorcontrib>Cool, Simon M</creatorcontrib><creatorcontrib>Hou, Han Wei</creatorcontrib><creatorcontrib>Han, Jongyoon</creatorcontrib><title>Scalable mesenchymal stem cell enrichment from bone marrow aspirate using deterministic lateral displacement (DLD) microfluidic sorting</title><title>Lab on a chip</title><description>The growing interest in regenerative medicine has opened new avenues for novel cell therapies using stem cells. Bone marrow aspirate (BMA) is an important source of stromal mesenchymal stem cells (MSCs). Conventional MSC harvesting from BMA relies on archaic centrifugation methods, often leading to poor yield due to osmotic stress, high centrifugation force, convoluted workflow, and long experimental time (∼2-3 hours). To address these issues, we have developed a scalable microfluidic technology based on deterministic lateral displacement (DLD) for MSC isolation. This passive, label-free cell sorting method capitalizes on the morphological differences between MSCs and blood cells (platelets and RBCs) for effective separation using an inverted L-shaped pillar array. To improve throughput, we developed a novel multi-chip DLD system that can process 2.5 mL of raw BMA in 20 ± 5 minutes, achieving a 2-fold increase in MSC recovery compared to centrifugation methods. Taken together, we envision that the developed DLD platform will enable fast and efficient isolation of MSCs from BMA for effective downstream cell therapy in clinical settings.
MSCs are enriched twice more efficiently with 10-fold shorten processing time from undiluted human bone marrow aspirate.</description><subject>Blood cells</subject><subject>Bone marrow</subject><subject>Lateral displacement</subject><subject>Microfluidics</subject><subject>Stem cells</subject><subject>Workflow</subject><issn>1473-0197</issn><issn>1473-0189</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpd0U1LwzAYB_AiCs7pxbsQ8KJCNWnapD3KNl-g4EE9lyR96jLSF5MU2Sfwa5ttMsFTAvnlT578o-ic4FuCaXFXU6MwpryAg2hCUk5jTPLicL8v-HF04twKY5KlLJ9E369KGCENoBYcdGq5boVBzkOLFBiDoLNaLVvoPGps3yLZd4EKa_svJNygrfCARqe7D1SDB9vqTjuvFTLhwIaoWrvBCAXbiKt5Ob9GrVa2b8yo6-Bcb324fRodNcI4OPtdp9H7w-Jt9hSXL4_Ps_syVjTDPpYZrZs6ZYRjkCqTXPBMMSAqLSjmMuciwSnUXHGWpbhRsmGSFEyKGsusaBSdRle73MH2nyM4X7XabSYVHfSjq5KcpSwhjCeBXv6jq360XXjdRuWM5BkmQd3sVJjJOQtNNVgdPmhdEVxtOqnmtJxtO1kEfLHD1qm9--uM_gBhrot5</recordid><startdate>20230926</startdate><enddate>20230926</enddate><creator>Tan Kwan Zen, Nicholas</creator><creator>Zeming, Kerwin Kwek</creator><creator>Teo, Kim Leng</creator><creator>Loberas, Mavis</creator><creator>Lee, Jialing</creator><creator>Goh, Chin Ren</creator><creator>Yang, Da Hou</creator><creator>Oh, Steve</creator><creator>Hui Hoi Po, James</creator><creator>Cool, Simon M</creator><creator>Hou, Han Wei</creator><creator>Han, Jongyoon</creator><general>Royal Society of Chemistry</general><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/0000-0001-6631-6321</orcidid><orcidid>https://orcid.org/0009-0004-0453-8577</orcidid><orcidid>https://orcid.org/0000-0001-8543-3056</orcidid><orcidid>https://orcid.org/0000-0001-7215-1439</orcidid><orcidid>https://orcid.org/0000-0002-3088-3604</orcidid></search><sort><creationdate>20230926</creationdate><title>Scalable mesenchymal stem cell enrichment from bone marrow aspirate using deterministic lateral displacement (DLD) microfluidic sorting</title><author>Tan Kwan Zen, Nicholas ; Zeming, Kerwin Kwek ; Teo, Kim Leng ; Loberas, Mavis ; Lee, Jialing ; Goh, Chin Ren ; Yang, Da Hou ; Oh, Steve ; Hui Hoi Po, James ; Cool, Simon M ; Hou, Han Wei ; Han, Jongyoon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-b53dfd46170ebc5b7a75c6e1c49307b87a204ed7c76540fcbf6b196bad0b59fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Blood cells</topic><topic>Bone marrow</topic><topic>Lateral displacement</topic><topic>Microfluidics</topic><topic>Stem cells</topic><topic>Workflow</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tan Kwan Zen, Nicholas</creatorcontrib><creatorcontrib>Zeming, Kerwin Kwek</creatorcontrib><creatorcontrib>Teo, Kim Leng</creatorcontrib><creatorcontrib>Loberas, Mavis</creatorcontrib><creatorcontrib>Lee, Jialing</creatorcontrib><creatorcontrib>Goh, Chin Ren</creatorcontrib><creatorcontrib>Yang, Da Hou</creatorcontrib><creatorcontrib>Oh, Steve</creatorcontrib><creatorcontrib>Hui Hoi Po, James</creatorcontrib><creatorcontrib>Cool, Simon M</creatorcontrib><creatorcontrib>Hou, Han Wei</creatorcontrib><creatorcontrib>Han, Jongyoon</creatorcontrib><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>Tan Kwan Zen, Nicholas</au><au>Zeming, Kerwin Kwek</au><au>Teo, Kim Leng</au><au>Loberas, Mavis</au><au>Lee, Jialing</au><au>Goh, Chin Ren</au><au>Yang, Da Hou</au><au>Oh, Steve</au><au>Hui Hoi Po, James</au><au>Cool, Simon M</au><au>Hou, Han Wei</au><au>Han, Jongyoon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Scalable mesenchymal stem cell enrichment from bone marrow aspirate using deterministic lateral displacement (DLD) microfluidic sorting</atitle><jtitle>Lab on a chip</jtitle><date>2023-09-26</date><risdate>2023</risdate><volume>23</volume><issue>19</issue><spage>4313</spage><epage>4323</epage><pages>4313-4323</pages><issn>1473-0197</issn><eissn>1473-0189</eissn><abstract>The growing interest in regenerative medicine has opened new avenues for novel cell therapies using stem cells. Bone marrow aspirate (BMA) is an important source of stromal mesenchymal stem cells (MSCs). Conventional MSC harvesting from BMA relies on archaic centrifugation methods, often leading to poor yield due to osmotic stress, high centrifugation force, convoluted workflow, and long experimental time (∼2-3 hours). To address these issues, we have developed a scalable microfluidic technology based on deterministic lateral displacement (DLD) for MSC isolation. This passive, label-free cell sorting method capitalizes on the morphological differences between MSCs and blood cells (platelets and RBCs) for effective separation using an inverted L-shaped pillar array. To improve throughput, we developed a novel multi-chip DLD system that can process 2.5 mL of raw BMA in 20 ± 5 minutes, achieving a 2-fold increase in MSC recovery compared to centrifugation methods. Taken together, we envision that the developed DLD platform will enable fast and efficient isolation of MSCs from BMA for effective downstream cell therapy in clinical settings.
MSCs are enriched twice more efficiently with 10-fold shorten processing time from undiluted human bone marrow aspirate.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d3lc00379e</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-6631-6321</orcidid><orcidid>https://orcid.org/0009-0004-0453-8577</orcidid><orcidid>https://orcid.org/0000-0001-8543-3056</orcidid><orcidid>https://orcid.org/0000-0001-7215-1439</orcidid><orcidid>https://orcid.org/0000-0002-3088-3604</orcidid><oa>free_for_read</oa></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Blood cells Bone marrow Lateral displacement Microfluidics Stem cells Workflow |
title | Scalable mesenchymal stem cell enrichment from bone marrow aspirate using deterministic lateral displacement (DLD) microfluidic sorting |
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