{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Fernandez A"],"funding":["Fundaci?n Alfonso Mart?n Escudero","H2020 Marie Sklodowska-Curie Actions","FP7 People: Marie-Curie Actions","Medical Research Council","Royal Society","Wellcome Trust","Biotechnology and Biological Sciences Research Council","Engineering and Physical Sciences Research Council"],"pagination":["995-1005"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5620981"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["3(9)"],"pubmed_abstract":["Immunomodulatory agents represent one of the most promising strategies for enhancing tissue regeneration without the side effects of traditional drug-based therapies. Tissue repair depends largely on macrophages, making them ideal targets for proregenerative therapies. However, given the multiple roles of macrophages in tissue homeostasis, small molecule drugs must be only active in very specific subpopulations. In this work, we have developed the first prodrug-fluorophore conjugates able to discriminate closely related subpopulations of macrophages (i.e., proinflammatory M1 vs anti-inflammatory M2 macrophages), and employed them to deplete M1 macrophages <i>in vivo</i> without affecting other cell populations. Selective intracellular activation and drug release enabled simultaneous fluore"],"journal":["ACS central science"],"pubmed_title":["Chemical Modulation of <i>in Vivo</i> Macrophage Function with Subpopulation-Specific Fluorescent Prodrug Conjugates."],"pmcid":["PMC5620981"],"funding_grant_id":["659046","333847","EP/L016559/1","100104/Z/12/Z","704912","BB/M025160/1","RG160289"],"pubmed_authors":["Humphries D","Vendrell M","Campana L","Vermeren M","Subiros-Funosas R","Feng Y","Barth N","Fernandez A","MacKinnon A"],"additional_accession":[]},"is_claimable":false,"name":"Chemical Modulation of <i>in Vivo</i> Macrophage Function with Subpopulation-Specific Fluorescent Prodrug Conjugates.","description":"Immunomodulatory agents represent one of the most promising strategies for enhancing tissue regeneration without the side effects of traditional drug-based therapies. Tissue repair depends largely on macrophages, making them ideal targets for proregenerative therapies. However, given the multiple roles of macrophages in tissue homeostasis, small molecule drugs must be only active in very specific subpopulations. In this work, we have developed the first prodrug-fluorophore conjugates able to discriminate closely related subpopulations of macrophages (i.e., proinflammatory M1 vs anti-inflammatory M2 macrophages), and employed them to deplete M1 macrophages <i>in vivo</i> without affecting other cell populations. Selective intracellular activation and drug release enabled simultaneous fluore","dates":{"release":"2017-01-01T00:00:00Z","publication":"2017 Sep","modification":"2025-05-29T21:57:26.211Z","creation":"2025-05-29T21:57:26.211Z"},"accession":"S-EPMC5620981","cross_references":{"pubmed":["28979941"],"doi":["10.1021/acscentsci.7b00262"]}}