<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(2)</volume><submitter>Murugesan G</submitter><pubmed_abstract>Macrophages (MΦ) are highly heterogenous and versatile innate immune cells involved in homeostatic and immune responses. Activated MΦ can exist in two extreme phenotypes: pro-inflammatory (M1) MΦ and anti-inflammatory (M2) MΦ. These phenotypes can be recapitulated in vitro by using ligands of toll-like receptors (TLRs) and cytokines such as IFNγ and IL-4. In recent years, human induced pluripotent stem cells (iPSC)-derived MΦ have gained major attention, as they are functionally similar to human monocyte-derived MΦ and are receptive to genome editing. In this study, we polarised iPSC-derived MΦ to M1 or M2 and analysed their proteome and secretome profiles using quantitative proteomics. These comprehensive proteomic data sets provide new insights into functions of polarised MΦ.</pubmed_abstract><journal>Biomedicines</journal><pagination>239</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8869710</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Quantitative Proteomics of Polarised Macrophages Derived from Induced Pluripotent Stem Cells.</pubmed_title><pmcid>PMC8869710</pmcid><pubmed_authors>Weigle B</pubmed_authors><pubmed_authors>Murugesan G</pubmed_authors><pubmed_authors>Crocker PR</pubmed_authors><pubmed_authors>Davidson L</pubmed_authors><pubmed_authors>Jannetti L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantitative Proteomics of Polarised Macrophages Derived from Induced Pluripotent Stem Cells.</name><description>Macrophages (MΦ) are highly heterogenous and versatile innate immune cells involved in homeostatic and immune responses. Activated MΦ can exist in two extreme phenotypes: pro-inflammatory (M1) MΦ and anti-inflammatory (M2) MΦ. These phenotypes can be recapitulated in vitro by using ligands of toll-like receptors (TLRs) and cytokines such as IFNγ and IL-4. In recent years, human induced pluripotent stem cells (iPSC)-derived MΦ have gained major attention, as they are functionally similar to human monocyte-derived MΦ and are receptive to genome editing. In this study, we polarised iPSC-derived MΦ to M1 or M2 and analysed their proteome and secretome profiles using quantitative proteomics. These comprehensive proteomic data sets provide new insights into functions of polarised MΦ.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-22T03:49:05.945Z</modification><creation>2025-04-05T20:50:16.325Z</creation></dates><accession>S-EPMC8869710</accession><cross_references><pubmed>35203449</pubmed><doi>10.3390/biomedicines10020239</doi></cross_references></HashMap>