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http://purl.uniprot.org/citations/37115584http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/37115584http://www.w3.org/2000/01/rdf-schema#comment"Hematopoietic stem cells (HSC) and downstream lineage-biased multipotent progenitors (MPP) tailor blood production and control myelopoiesis on demand. Recent lineage tracing analyses revealed MPPs to be major functional contributors to steady-state hematopoiesis. However, we still lack a precise resolution of myeloid differentiation trajectories and cellular heterogeneity in the MPP compartment. Here, we found that myeloid-biased MPP3 are functionally and molecularly heterogeneous, with a distinct subset of myeloid-primed secretory cells with high endoplasmic reticulum (ER) volume and FcγR expression. We show that FcγR+/ERhigh MPP3 are a transitional population serving as a reservoir for rapid production of granulocyte/macrophage progenitors (GMP), which directly amplify myelopoiesis through inflammation-triggered secretion of cytokines in the local bone marrow (BM) microenvironment. Our results identify a novel regulatory function for a secretory MPP3 subset that controls myeloid differentiation through lineage-priming and cytokine production and acts as a self-reinforcing amplification compartment in inflammatory stress and disease conditions."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.org/dc/terms/identifier"doi:10.1084/jem.20230088"xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Fan R."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Zhang S.Y."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Chen J.J."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Mitchell C.A."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Collins A."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Kang Y.A."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Passegue E."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Warr M.R."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Swann J.W."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Olson O.C."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/author"Paik H."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/date"2023"xsd:gYear
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/name"J Exp Med"xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/pages"e20230088"xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/title"Secretory MPP3 reinforce myeloid differentiation trajectory and amplify myeloid cell production."xsd:string
http://purl.uniprot.org/citations/37115584http://purl.uniprot.org/core/volume"220"xsd:string
http://purl.uniprot.org/citations/37115584http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/37115584
http://purl.uniprot.org/citations/37115584http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/37115584
http://purl.uniprot.org/uniprot/#_D3YVT4-mappedCitation-37115584http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37115584
http://purl.uniprot.org/uniprot/#_A0A0R4J210-mappedCitation-37115584http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37115584
http://purl.uniprot.org/uniprot/#_A0A0U5J4W4-mappedCitation-37115584http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37115584
http://purl.uniprot.org/uniprot/#_A0A2I3BRE5-mappedCitation-37115584http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/37115584