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Lipid Signatures and Inter-Cellular Heterogeneity of Naı̈ve and Lipopolysaccharide-Stimulated Human Microglia-like Cells
Microglia are non-neuronal cells, which reside in the central nervous system and are known to play an important role in health and disease. We investigated the lipidomic phenotypes of human naı̈ve and stimulated microglia-like cells by atmospheric-pressure scanning microprobe matrix-assisted laser d...
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Published in: | Analytical chemistry (Washington) 2023-08, Vol.95 (31), p.11672-11679 |
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creator | Müller, Max A. Zweig, Norman Spengler, Bernhard Weinert, Maria Heiles, Sven |
description | Microglia are non-neuronal cells, which reside in the central nervous system and are known to play an important role in health and disease. We investigated the lipidomic phenotypes of human naı̈ve and stimulated microglia-like cells by atmospheric-pressure scanning microprobe matrix-assisted laser desorption/ionization mass spectrometry imaging (AP-SMALDI MSI). With lateral resolutions between 5 and 1.5 μm pixel size, we were able to chart lipid compositions of individual cells, enabling differentiation of cell lines and stimulation conditions. This allowed us to reveal local lipid heterogeneities in naı̈ve and lipopolysaccharide (LPS)-stimulated cells. We were able to identify individual cells with elevated triglyceride (TG) levels and could show that the number of these TG-enriched cells increased with LPS stimulation as a hallmark for a proinflammatory phenotype. Additionally, the observed local abundance alterations of specific phosphatidylinositols (PIs) indicate a cell specific regulation of the PI metabolism. |
doi_str_mv | 10.1021/acs.analchem.3c01533 |
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We investigated the lipidomic phenotypes of human naı̈ve and stimulated microglia-like cells by atmospheric-pressure scanning microprobe matrix-assisted laser desorption/ionization mass spectrometry imaging (AP-SMALDI MSI). With lateral resolutions between 5 and 1.5 μm pixel size, we were able to chart lipid compositions of individual cells, enabling differentiation of cell lines and stimulation conditions. This allowed us to reveal local lipid heterogeneities in naı̈ve and lipopolysaccharide (LPS)-stimulated cells. We were able to identify individual cells with elevated triglyceride (TG) levels and could show that the number of these TG-enriched cells increased with LPS stimulation as a hallmark for a proinflammatory phenotype. Additionally, the observed local abundance alterations of specific phosphatidylinositols (PIs) indicate a cell specific regulation of the PI metabolism.</description><identifier>ISSN: 0003-2700</identifier><identifier>EISSN: 1520-6882</identifier><identifier>DOI: 10.1021/acs.analchem.3c01533</identifier><identifier>PMID: 37506282</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Analytical chemistry ; Cell Differentiation ; Cell lines ; Central nervous system ; Chemistry ; Heterogeneity ; Humans ; Inflammation ; Ionization ; Lipids ; Lipopolysaccharides ; Lipopolysaccharides - pharmacology ; Mass spectrometry ; Mass spectroscopy ; Metabolism ; Microglia ; Phenotypes ; Phosphatidylinositols ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods ; Stimulation ; Triglycerides</subject><ispartof>Analytical chemistry (Washington), 2023-08, Vol.95 (31), p.11672-11679</ispartof><rights>2023 American Chemical Society</rights><rights>Copyright American Chemical Society Aug 8, 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a2863-1ccac1ccccbc6fd4c68d366958514d06f740ca0bf54976874daf3f3d1db226ab3</cites><orcidid>0000-0003-0179-5653 ; 0000-0002-9960-5020 ; 0000-0003-3779-8071</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37506282$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Müller, Max A.</creatorcontrib><creatorcontrib>Zweig, Norman</creatorcontrib><creatorcontrib>Spengler, Bernhard</creatorcontrib><creatorcontrib>Weinert, Maria</creatorcontrib><creatorcontrib>Heiles, Sven</creatorcontrib><title>Lipid Signatures and Inter-Cellular Heterogeneity of Naı̈ve and Lipopolysaccharide-Stimulated Human Microglia-like Cells</title><title>Analytical chemistry (Washington)</title><addtitle>Anal. Chem</addtitle><description>Microglia are non-neuronal cells, which reside in the central nervous system and are known to play an important role in health and disease. We investigated the lipidomic phenotypes of human naı̈ve and stimulated microglia-like cells by atmospheric-pressure scanning microprobe matrix-assisted laser desorption/ionization mass spectrometry imaging (AP-SMALDI MSI). With lateral resolutions between 5 and 1.5 μm pixel size, we were able to chart lipid compositions of individual cells, enabling differentiation of cell lines and stimulation conditions. This allowed us to reveal local lipid heterogeneities in naı̈ve and lipopolysaccharide (LPS)-stimulated cells. We were able to identify individual cells with elevated triglyceride (TG) levels and could show that the number of these TG-enriched cells increased with LPS stimulation as a hallmark for a proinflammatory phenotype. Additionally, the observed local abundance alterations of specific phosphatidylinositols (PIs) indicate a cell specific regulation of the PI metabolism.</description><subject>Analytical chemistry</subject><subject>Cell Differentiation</subject><subject>Cell lines</subject><subject>Central nervous system</subject><subject>Chemistry</subject><subject>Heterogeneity</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Ionization</subject><subject>Lipids</subject><subject>Lipopolysaccharides</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Metabolism</subject><subject>Microglia</subject><subject>Phenotypes</subject><subject>Phosphatidylinositols</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</subject><subject>Stimulation</subject><subject>Triglycerides</subject><issn>0003-2700</issn><issn>1520-6882</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kc1OGzEURq0KVNK0b1AhS2zYTLi2Z-zJEkXQREphAV2P7tgeYjo_wZ5BCk_Q1-k7dNmHqtOELFiwsWXpfMfX_gj5ymDCgLML1GGCLdZ6ZZuJ0MAyIT6QEcs4JDLP-REZAYBIuAI4IZ9CeARgDJj8SE6EykDynI_Iy9KtnaF37qHFfvA2UGwNXbS99cnM1vVQo6dzG4_dg22t6ze0q-gN_vn999ez_Q9HQ7fu6k1ArVfonbHJXe-amOytofOhwZZ-dzoKaodJ7X5aujWHz-S4wjrYL_t9TH5cX93P5sny9ttidrlMkOdSJExr1HHRutSyMqmWuRFSTrM8Y6kBWakUNEJZZelUyVylBitRCcNMybnEUozJ-c679t3TYENfNC7oOAG2thtCwfNUqVQxJiN69gZ97AYfP3lHTYUSGYtUuqPim0LwtirW3jXoNwWDYttNEbspXrsp9t3E2OlePpSNNYfQaxkRgB2wjR8uftf5Dx6EoM8</recordid><startdate>20230808</startdate><enddate>20230808</enddate><creator>Müller, Max A.</creator><creator>Zweig, Norman</creator><creator>Spengler, Bernhard</creator><creator>Weinert, Maria</creator><creator>Heiles, Sven</creator><general>American Chemical Society</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>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7TM</scope><scope>7U5</scope><scope>7U7</scope><scope>7U9</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0179-5653</orcidid><orcidid>https://orcid.org/0000-0002-9960-5020</orcidid><orcidid>https://orcid.org/0000-0003-3779-8071</orcidid></search><sort><creationdate>20230808</creationdate><title>Lipid Signatures and Inter-Cellular Heterogeneity of Naı̈ve and Lipopolysaccharide-Stimulated Human Microglia-like Cells</title><author>Müller, Max A. ; 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subjects | Analytical chemistry Cell Differentiation Cell lines Central nervous system Chemistry Heterogeneity Humans Inflammation Ionization Lipids Lipopolysaccharides Lipopolysaccharides - pharmacology Mass spectrometry Mass spectroscopy Metabolism Microglia Phenotypes Phosphatidylinositols Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods Stimulation Triglycerides |
title | Lipid Signatures and Inter-Cellular Heterogeneity of Naı̈ve and Lipopolysaccharide-Stimulated Human Microglia-like Cells |
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