Five‐in‐One: Simultaneous isolation of multiple major liver cell types from livers of normal and NASH mice
NASH is a chronic liver disease that affects 3%–6% of individuals and requires urgent therapeutic developments. Isolating the key cell types in the liver is a necessary step towards understanding their function and roles in disease pathogenesis. However, traditional isolation methods through gradien...
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Veröffentlicht in: | Journal of cellular and molecular medicine 2021-10, Vol.25 (20), p.9878-9883 |
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description | NASH is a chronic liver disease that affects 3%–6% of individuals and requires urgent therapeutic developments. Isolating the key cell types in the liver is a necessary step towards understanding their function and roles in disease pathogenesis. However, traditional isolation methods through gradient centrifugation can only collect one or a few cell types simultaneously and pose technical difficulties when applied to NASH livers. Taking advantage of identified cell surface markers from liver single‐cell RNAseq, here we established the combination of gradient centrifugation and antibody‐based cell sorting techniques to isolate five key liver cell types (hepatocytes, endothelial cells, stellate cells, macrophages and other immune cells) from a single mouse liver. This method yielded high purity of each cell type from healthy and NASH livers. Our five‐in‐one protocol simultaneously isolates key liver cell types with high purity under normal and NASH conditions, enabling for systematic and accurate exploratory experiments such as RNA sequencing. |
doi_str_mv | 10.1111/jcmm.16933 |
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Isolating the key cell types in the liver is a necessary step towards understanding their function and roles in disease pathogenesis. However, traditional isolation methods through gradient centrifugation can only collect one or a few cell types simultaneously and pose technical difficulties when applied to NASH livers. Taking advantage of identified cell surface markers from liver single‐cell RNAseq, here we established the combination of gradient centrifugation and antibody‐based cell sorting techniques to isolate five key liver cell types (hepatocytes, endothelial cells, stellate cells, macrophages and other immune cells) from a single mouse liver. This method yielded high purity of each cell type from healthy and NASH livers. Our five‐in‐one protocol simultaneously isolates key liver cell types with high purity under normal and NASH conditions, enabling for systematic and accurate exploratory experiments such as RNA sequencing.</description><identifier>ISSN: 1582-1838</identifier><identifier>EISSN: 1582-4934</identifier><identifier>DOI: 10.1111/jcmm.16933</identifier><identifier>PMID: 34558178</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Animals ; Biomarkers ; cell isolation ; Cell Separation - methods ; Cell surface ; Centrifugation ; Diet ; Disease Models, Animal ; Endothelial cells ; Endothelial Cells - metabolism ; Experiments ; Flow cytometry ; fluorescence‐activated cell sorting ; Fluorescent Antibody Technique ; Gene expression ; Hepatocytes ; Hepatocytes - metabolism ; Immunophenotyping ; Liver ; Liver - cytology ; Liver diseases ; Macrophages ; Macrophages - metabolism ; Male ; Methods ; Mice ; Morphology ; Non-alcoholic Fatty Liver Disease - etiology ; Non-alcoholic Fatty Liver Disease - pathology ; non‐alcoholic steatohepatitis ; Pathogenesis ; Short Communication ; Short Communications ; Stellate cells ; Surface markers</subject><ispartof>Journal of cellular and molecular medicine, 2021-10, Vol.25 (20), p.9878-9883</ispartof><rights>2021 Regeneron Pharmaceuticals, Inc. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.</rights><rights>2021 Regeneron Pharmaceuticals, Inc. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4483-3a9784eb4953cf701711a793628b25875eb26a77dbc79b7112dd1c5800b4c7333</citedby><cites>FETCH-LOGICAL-c4483-3a9784eb4953cf701711a793628b25875eb26a77dbc79b7112dd1c5800b4c7333</cites><orcidid>0000-0003-3861-3120</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505823/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505823/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1416,11561,27923,27924,45573,45574,46051,46475,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34558178$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhou, Ye</creatorcontrib><creatorcontrib>Adewale, Funmilola</creatorcontrib><creatorcontrib>Kim, Sun</creatorcontrib><creatorcontrib>Su, Qi</creatorcontrib><creatorcontrib>Glass, David</creatorcontrib><creatorcontrib>Sleeman, Mark W.</creatorcontrib><creatorcontrib>Murphy, Andrew J.</creatorcontrib><creatorcontrib>Cheng, Xiping</creatorcontrib><title>Five‐in‐One: Simultaneous isolation of multiple major liver cell types from livers of normal and NASH mice</title><title>Journal of cellular and molecular medicine</title><addtitle>J Cell Mol Med</addtitle><description>NASH is a chronic liver disease that affects 3%–6% of individuals and requires urgent therapeutic developments. Isolating the key cell types in the liver is a necessary step towards understanding their function and roles in disease pathogenesis. However, traditional isolation methods through gradient centrifugation can only collect one or a few cell types simultaneously and pose technical difficulties when applied to NASH livers. Taking advantage of identified cell surface markers from liver single‐cell RNAseq, here we established the combination of gradient centrifugation and antibody‐based cell sorting techniques to isolate five key liver cell types (hepatocytes, endothelial cells, stellate cells, macrophages and other immune cells) from a single mouse liver. This method yielded high purity of each cell type from healthy and NASH livers. Our five‐in‐one protocol simultaneously isolates key liver cell types with high purity under normal and NASH conditions, enabling for systematic and accurate exploratory experiments such as RNA sequencing.</description><subject>Animals</subject><subject>Biomarkers</subject><subject>cell isolation</subject><subject>Cell Separation - methods</subject><subject>Cell surface</subject><subject>Centrifugation</subject><subject>Diet</subject><subject>Disease Models, Animal</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - metabolism</subject><subject>Experiments</subject><subject>Flow cytometry</subject><subject>fluorescence‐activated cell sorting</subject><subject>Fluorescent Antibody Technique</subject><subject>Gene expression</subject><subject>Hepatocytes</subject><subject>Hepatocytes - metabolism</subject><subject>Immunophenotyping</subject><subject>Liver</subject><subject>Liver - cytology</subject><subject>Liver diseases</subject><subject>Macrophages</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Methods</subject><subject>Mice</subject><subject>Morphology</subject><subject>Non-alcoholic Fatty Liver Disease - etiology</subject><subject>Non-alcoholic Fatty Liver Disease - pathology</subject><subject>non‐alcoholic steatohepatitis</subject><subject>Pathogenesis</subject><subject>Short Communication</subject><subject>Short Communications</subject><subject>Stellate cells</subject><subject>Surface markers</subject><issn>1582-1838</issn><issn>1582-4934</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc9u1DAQxq0K1JaFSx8AWeKCkLbYsR07HJCqFaWglh7ani3HcYpX_rPYSdHeeASekSfBIUsFPdQH25r5zaeZ-QA4wugYl_N2rb0_xnVDyB44xExUS9oQ-mT3x4KIA_As5zVCpMak2QcHhDImMBeHIJzaO_Prx08bynUZzDt4Zf3oBhVMHDO0OTo12Bhg7OEUtxtnoFfrmKArlQlq4xwcthuTYZ-in6N5wkNMXjmoQge_nFydQW-1eQ6e9spl82L3LsDN6Yfr1dny_PLjp9XJ-VJTKsiSqIYLalraMKJ7jjDHWPGG1JVoKyY4M21VK867VvOmLcmq67BmAqGWak4IWYD3s-5mbL3ptAlDUk5ukvUqbWVUVv6fCfarvI13UjBUljYJvN4JpPhtNHmQ3uZp1nkxsmK8rlmFKCroqwfoOo4plPEKJZAgZJppAd7MlE4x52T6-2YwkpONcrJR_rGxwC__bf8e_etbAfAMfLfObB-Rkp9XFxez6G_3PKoS</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Zhou, Ye</creator><creator>Adewale, Funmilola</creator><creator>Kim, Sun</creator><creator>Su, Qi</creator><creator>Glass, David</creator><creator>Sleeman, Mark W.</creator><creator>Murphy, Andrew J.</creator><creator>Cheng, Xiping</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3861-3120</orcidid></search><sort><creationdate>202110</creationdate><title>Five‐in‐One: Simultaneous isolation of multiple major liver cell types from livers of normal and NASH mice</title><author>Zhou, Ye ; Adewale, Funmilola ; Kim, Sun ; Su, Qi ; Glass, David ; Sleeman, Mark W. ; Murphy, Andrew J. ; Cheng, Xiping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4483-3a9784eb4953cf701711a793628b25875eb26a77dbc79b7112dd1c5800b4c7333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Biomarkers</topic><topic>cell isolation</topic><topic>Cell Separation - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cellular and molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Ye</au><au>Adewale, Funmilola</au><au>Kim, Sun</au><au>Su, Qi</au><au>Glass, David</au><au>Sleeman, Mark W.</au><au>Murphy, Andrew J.</au><au>Cheng, Xiping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Five‐in‐One: Simultaneous isolation of multiple major liver cell types from livers of normal and NASH mice</atitle><jtitle>Journal of cellular and molecular medicine</jtitle><addtitle>J Cell Mol Med</addtitle><date>2021-10</date><risdate>2021</risdate><volume>25</volume><issue>20</issue><spage>9878</spage><epage>9883</epage><pages>9878-9883</pages><issn>1582-1838</issn><eissn>1582-4934</eissn><abstract>NASH is a chronic liver disease that affects 3%–6% of individuals and requires urgent therapeutic developments. Isolating the key cell types in the liver is a necessary step towards understanding their function and roles in disease pathogenesis. However, traditional isolation methods through gradient centrifugation can only collect one or a few cell types simultaneously and pose technical difficulties when applied to NASH livers. Taking advantage of identified cell surface markers from liver single‐cell RNAseq, here we established the combination of gradient centrifugation and antibody‐based cell sorting techniques to isolate five key liver cell types (hepatocytes, endothelial cells, stellate cells, macrophages and other immune cells) from a single mouse liver. This method yielded high purity of each cell type from healthy and NASH livers. Our five‐in‐one protocol simultaneously isolates key liver cell types with high purity under normal and NASH conditions, enabling for systematic and accurate exploratory experiments such as RNA sequencing.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>34558178</pmid><doi>10.1111/jcmm.16933</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-3861-3120</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomarkers cell isolation Cell Separation - methods Cell surface Centrifugation Diet Disease Models, Animal Endothelial cells Endothelial Cells - metabolism Experiments Flow cytometry fluorescence‐activated cell sorting Fluorescent Antibody Technique Gene expression Hepatocytes Hepatocytes - metabolism Immunophenotyping Liver Liver - cytology Liver diseases Macrophages Macrophages - metabolism Male Methods Mice Morphology Non-alcoholic Fatty Liver Disease - etiology Non-alcoholic Fatty Liver Disease - pathology non‐alcoholic steatohepatitis Pathogenesis Short Communication Short Communications Stellate cells Surface markers |
title | Five‐in‐One: Simultaneous isolation of multiple major liver cell types from livers of normal and NASH mice |
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