Optimization of pre-enrichment strategies for mouse hematopoietic stem cell isolation and metabolomic analysis
•Performing a pre-enrichment can increase HSC frequency more than 30-fold.•Lineage depletion is the fastest strategy, while c-Kit or Sca-1 selection give the highest enrichment.•Combining two pre-enrichment strategies increases stem cell frequency at the cost of final yield.•c-Kit enrichment appears...
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Veröffentlicht in: | Experimental hematology 2024-11, Vol.139, p.104588, Article 104588 |
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creator | Nielsen, Célina Liu, Youzhong Leguay, Fleur Tirado, Hernán A. Dauguet, Nicolas van Gastel, Nick |
description | •Performing a pre-enrichment can increase HSC frequency more than 30-fold.•Lineage depletion is the fastest strategy, while c-Kit or Sca-1 selection give the highest enrichment.•Combining two pre-enrichment strategies increases stem cell frequency at the cost of final yield.•c-Kit enrichment appears optimal for metabolomics analysis of HSCs.
Blood cell production arises from the activity of hematopoietic stem cells (HSCs), defined by their self-renewal capacity and ability to give rise to all mature blood cell types. The mouse remains one of the most studied species in hematological research, and markers to define and isolate mouse HSCs are well-established. Given the very low frequency of HSCs in the bone marrow, stem cell pre-enrichment by red blood cell lysis and magnetic cell separation is often performed as part of the isolation process to reduce sorting times. Several pre-enrichment strategies are available, differing in their speed, degree of enrichment, final cell yield, and cost. In the current study, we performed a side-by-side comparison and provide a decision tree to help researchers select a pre-enrichment strategy for mouse HSC isolation depending on their downstream application. We then compared different pre-enrichment techniques in combination with metabolomics analysis of HSCs, where speed, yield and temperature during pre-enrichment are crucial factors, and found that the choice of pre-enrichment strategy significantly impacts the number of metabolites detected and levels of individual metabolites in HSCs. |
doi_str_mv | 10.1016/j.exphem.2024.104588 |
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Blood cell production arises from the activity of hematopoietic stem cells (HSCs), defined by their self-renewal capacity and ability to give rise to all mature blood cell types. The mouse remains one of the most studied species in hematological research, and markers to define and isolate mouse HSCs are well-established. Given the very low frequency of HSCs in the bone marrow, stem cell pre-enrichment by red blood cell lysis and magnetic cell separation is often performed as part of the isolation process to reduce sorting times. Several pre-enrichment strategies are available, differing in their speed, degree of enrichment, final cell yield, and cost. In the current study, we performed a side-by-side comparison and provide a decision tree to help researchers select a pre-enrichment strategy for mouse HSC isolation depending on their downstream application. We then compared different pre-enrichment techniques in combination with metabolomics analysis of HSCs, where speed, yield and temperature during pre-enrichment are crucial factors, and found that the choice of pre-enrichment strategy significantly impacts the number of metabolites detected and levels of individual metabolites in HSCs.</description><identifier>ISSN: 0301-472X</identifier><identifier>ISSN: 1873-2399</identifier><identifier>EISSN: 1873-2399</identifier><identifier>DOI: 10.1016/j.exphem.2024.104588</identifier><identifier>PMID: 39097159</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><ispartof>Experimental hematology, 2024-11, Vol.139, p.104588, Article 104588</ispartof><rights>2024 International Society for Experimental Hematology</rights><rights>Copyright © 2024 International Society for Experimental Hematology. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c241t-494f6dad1308aa3391fa16e725e94e10e47cc439d370d225f3842e988694d2103</cites><orcidid>0000-0002-0563-3590 ; 0009-0006-0299-6480</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.exphem.2024.104588$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39097159$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nielsen, Célina</creatorcontrib><creatorcontrib>Liu, Youzhong</creatorcontrib><creatorcontrib>Leguay, Fleur</creatorcontrib><creatorcontrib>Tirado, Hernán A.</creatorcontrib><creatorcontrib>Dauguet, Nicolas</creatorcontrib><creatorcontrib>van Gastel, Nick</creatorcontrib><title>Optimization of pre-enrichment strategies for mouse hematopoietic stem cell isolation and metabolomic analysis</title><title>Experimental hematology</title><addtitle>Exp Hematol</addtitle><description>•Performing a pre-enrichment can increase HSC frequency more than 30-fold.•Lineage depletion is the fastest strategy, while c-Kit or Sca-1 selection give the highest enrichment.•Combining two pre-enrichment strategies increases stem cell frequency at the cost of final yield.•c-Kit enrichment appears optimal for metabolomics analysis of HSCs.
Blood cell production arises from the activity of hematopoietic stem cells (HSCs), defined by their self-renewal capacity and ability to give rise to all mature blood cell types. The mouse remains one of the most studied species in hematological research, and markers to define and isolate mouse HSCs are well-established. Given the very low frequency of HSCs in the bone marrow, stem cell pre-enrichment by red blood cell lysis and magnetic cell separation is often performed as part of the isolation process to reduce sorting times. Several pre-enrichment strategies are available, differing in their speed, degree of enrichment, final cell yield, and cost. In the current study, we performed a side-by-side comparison and provide a decision tree to help researchers select a pre-enrichment strategy for mouse HSC isolation depending on their downstream application. We then compared different pre-enrichment techniques in combination with metabolomics analysis of HSCs, where speed, yield and temperature during pre-enrichment are crucial factors, and found that the choice of pre-enrichment strategy significantly impacts the number of metabolites detected and levels of individual metabolites in HSCs.</description><issn>0301-472X</issn><issn>1873-2399</issn><issn>1873-2399</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kM1KJDEUhYMo2tP6BiJZuqk2f_WTjSAyOgOCGwV3IZ3c0jSVSpmkRX36SVPqclaBy3fPyf0QOqVkRQltLjYreJ9ewK8YYaKMRN11e2hBu5ZXjEu5jxaEE1qJlj0doV8pbQghdS3JITriksiW1nKBxvspO-8-dXZhxKHHU4QKxujMi4cx45SjzvDsIOE-ROzDNgEurTqHKTjIzhQEPDYwDNilMMxBerTYQ9brMARfGD3q4SO5dIwOej0kOPl6l-jx5vfD9Z_q7v727_XVXWWYoLkSUvSN1ZZy0mnNuaS9pg20rAYpgBIQrTGCS8tbYhmre94JBrLrGikso4Qv0fmcO8XwuoWUlXdp90c9QjlBldy2kV3d8oKKGTUxpBShV1N0XscPRYnamVYbNZtWO9NqNl3Wzr4atmsP9mfpW20BLmcAyp1vDqJKxsFowLoIJisb3P8b_gHvxpL2</recordid><startdate>20241101</startdate><enddate>20241101</enddate><creator>Nielsen, Célina</creator><creator>Liu, Youzhong</creator><creator>Leguay, Fleur</creator><creator>Tirado, Hernán A.</creator><creator>Dauguet, Nicolas</creator><creator>van Gastel, Nick</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0563-3590</orcidid><orcidid>https://orcid.org/0009-0006-0299-6480</orcidid></search><sort><creationdate>20241101</creationdate><title>Optimization of pre-enrichment strategies for mouse hematopoietic stem cell isolation and metabolomic analysis</title><author>Nielsen, Célina ; Liu, Youzhong ; Leguay, Fleur ; Tirado, Hernán A. ; Dauguet, Nicolas ; van Gastel, Nick</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-494f6dad1308aa3391fa16e725e94e10e47cc439d370d225f3842e988694d2103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nielsen, Célina</creatorcontrib><creatorcontrib>Liu, Youzhong</creatorcontrib><creatorcontrib>Leguay, Fleur</creatorcontrib><creatorcontrib>Tirado, Hernán A.</creatorcontrib><creatorcontrib>Dauguet, Nicolas</creatorcontrib><creatorcontrib>van Gastel, Nick</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nielsen, Célina</au><au>Liu, Youzhong</au><au>Leguay, Fleur</au><au>Tirado, Hernán A.</au><au>Dauguet, Nicolas</au><au>van Gastel, Nick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimization of pre-enrichment strategies for mouse hematopoietic stem cell isolation and metabolomic analysis</atitle><jtitle>Experimental hematology</jtitle><addtitle>Exp Hematol</addtitle><date>2024-11-01</date><risdate>2024</risdate><volume>139</volume><spage>104588</spage><pages>104588-</pages><artnum>104588</artnum><issn>0301-472X</issn><issn>1873-2399</issn><eissn>1873-2399</eissn><abstract>•Performing a pre-enrichment can increase HSC frequency more than 30-fold.•Lineage depletion is the fastest strategy, while c-Kit or Sca-1 selection give the highest enrichment.•Combining two pre-enrichment strategies increases stem cell frequency at the cost of final yield.•c-Kit enrichment appears optimal for metabolomics analysis of HSCs.
Blood cell production arises from the activity of hematopoietic stem cells (HSCs), defined by their self-renewal capacity and ability to give rise to all mature blood cell types. The mouse remains one of the most studied species in hematological research, and markers to define and isolate mouse HSCs are well-established. Given the very low frequency of HSCs in the bone marrow, stem cell pre-enrichment by red blood cell lysis and magnetic cell separation is often performed as part of the isolation process to reduce sorting times. Several pre-enrichment strategies are available, differing in their speed, degree of enrichment, final cell yield, and cost. In the current study, we performed a side-by-side comparison and provide a decision tree to help researchers select a pre-enrichment strategy for mouse HSC isolation depending on their downstream application. We then compared different pre-enrichment techniques in combination with metabolomics analysis of HSCs, where speed, yield and temperature during pre-enrichment are crucial factors, and found that the choice of pre-enrichment strategy significantly impacts the number of metabolites detected and levels of individual metabolites in HSCs.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>39097159</pmid><doi>10.1016/j.exphem.2024.104588</doi><orcidid>https://orcid.org/0000-0002-0563-3590</orcidid><orcidid>https://orcid.org/0009-0006-0299-6480</orcidid><oa>free_for_read</oa></addata></record> |
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title | Optimization of pre-enrichment strategies for mouse hematopoietic stem cell isolation and metabolomic analysis |
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