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http://purl.uniprot.org/citations/35993548http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/35993548http://www.w3.org/2000/01/rdf-schema#comment"Dendritic cells (DCs) play an important role in anti-tumor immunity by inducing T cell differentiation. Herein, we found that the DC mechanical sensor Piezo1 stimulated by mechanical stiffness or inflammatory signals directs the reciprocal differentiation of TH1 and regulatory T (Treg) cells in cancer. Genetic deletion of Piezo1 in DCs inhibited the generation of TH1 cells while driving the development of Treg cells in promoting cancer growth in mice. Mechanistically, Piezo1-deficient DCs regulated the secretion of the polarizing cytokines TGFβ1 and IL-12, leading to increased TGFβR2-p-Smad3 activity and decreased IL-12Rβ2-p-STAT4 activity while inducing the reciprocal differentiation of Treg and TH1 cells. In addition, Piezo1 integrated the SIRT1-hypoxia-inducible factor-1 alpha (HIF1α)-dependent metabolic pathway and calcium-calcineurin-NFAT signaling pathway to orchestrate reciprocal TH1 and Treg lineage commitment through DC-derived IL-12 and TGFβ1. Our studies provide critical insight for understanding the role of the DC-based mechanical regulation of immunopathology in directing T cell lineage commitment in tumor microenvironments."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.org/dc/terms/identifier"doi:10.7554/elife.79957"xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Dong L."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Cao Y."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Hou Y."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Dong Y."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Liu G."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Bi Y."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Yang Q."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Yang H."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Wang Y.'"xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/author"Jia A."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/name"Elife"xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/pages"e79957"xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/title"Dendritic cell Piezo1 directs the differentiation of TH1 and Treg cells in cancer."xsd:string
http://purl.uniprot.org/citations/35993548http://purl.uniprot.org/core/volume"11"xsd:string
http://purl.uniprot.org/citations/35993548http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/35993548
http://purl.uniprot.org/citations/35993548http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/35993548
http://purl.uniprot.org/uniprot/#_A0A0R4J1E9-mappedCitation-35993548http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35993548
http://purl.uniprot.org/uniprot/#_A0A0R4J1F0-mappedCitation-35993548http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35993548
http://purl.uniprot.org/uniprot/#_A7MCT8-mappedCitation-35993548http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35993548
http://purl.uniprot.org/uniprot/#_F6YAQ3-mappedCitation-35993548http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/35993548