Cited by 298Hematopoietic Stem Cell TransplantationAcute Myeloid Leukemia ResearchBlood disorders and treatments

The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.

PU.1 regulates the commitment of adult hematopoietic progenitors and restricts granulopoiesis

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Dakic, Aleksandar, Metcalf, Donald, Di Rago, Ladina, Mifsud, Sandra, Wu, Li, Nutt, Stephen L.·2005·The Journal of Experimental Medicine

Abstract

Although the transcription factor PU.1 is essential for fetal lymphomyelopoiesis, we unexpectedly found that elimination of the gene in adult mice allowed disturbed hematopoiesis, dominated by granulocyte production. Impaired production of lymphocytes was evident in PU.1-deficient bone marrow (BM), but myelocytes and clonogenic granulocytic progenitors that are responsive to granulocyte colony-stimulating factor or interleukin-3 increased dramatically. No identifiable common lymphoid or myeloid progenitor populations were discernable by flow cytometry; however, clonogenic assays suggested an overall increased frequency of blast colony-forming cells and BM chimeras revealed existence of long-term self-renewing PU.1-deficient cells that required PU.1 for lymphoid, but not granulocyte, generation. PU.1 deletion in granulocyte-macrophage progenitors, but not in common myeloid progenitors, resulted in excess granulocyte production; this suggested specific roles of PU.1 at different stages of myeloid development. These findings emphasize the distinct nature of adult hematopoiesis and reveal that PU.1 regulates the specification of the multipotent lymphoid and myeloid compartments and restrains, rather than promotes, granulopoiesis.

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  1. 2004, Blood., 104, 3437
  2. 1996, Curr. Top. Microbiol. Immunol., 211, 137
  3. 1995, Oncogene., 11, 1549
  4. 1995, Leukemia., 9, 1556
  5. 1992, Exp. Hematol., 20, 600

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Items 201–298 of 298

Metadata

Authors
Dakic, A., Metcalf, D., Di Rago, L., Mifsud, S., Wu, L., & Nutt, S. L.
Affiliations
  • Walter and Eliza Hall Institute of Medical Research (AU)
  • The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3050, Australia
Venue
The Journal of Experimental Medicine
Published
2005-05-02
Volume
201
Issue
9
Pages
1487-1502
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
OpenAlex
W2136610354
Cited by
297
References
51
Citations by year
2026: 4 · 2025: 4 · 2024: 15 · 2023: 13 · 2022: 6 · 2021: 9 · 2020: 7 · 2019: 12 · 2018: 13 · 2017: 17 · 2016: 9 · 2015: 18 · 2014: 15 · 2013: 26 · 2012: 21
FWCI
10.47
Type
journal article
Language
en
Open access
Licence
cc-by-nc-sa
Locations
  • The Journal of Experimental Medicine (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
  • Minerva Access (University of Melbourne) (submittedVersion, cc-by-nc-sa)
Funders
  • National Institutes of Health (CA22556)
  • Medical Research Council
  • National Health and Medical Research Council
  • Cancer Council Victoria
  • National Cancer Institute (R37CA022556, CA22556, R01CA022556)
Topics
  • Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
  • Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
  • Health Sciences › Medicine › Hematology › Blood disorders and treatments
Keywords
PU.1, granulopoiesis, hematopoietic progenitor cells, CFU-GM, common myeloid progenitors, lymphocyte production, granulocyte colony-stimulating factor, interleukin-3, bone marrow chimeras, transcription factors, adult hematopoiesis
MeSH terms
Proto-Oncogene Protein Spi-1, Animals, Antibodies, Monoclonal, Blood Cell Count, Cell Differentiation, Cells, Cultured, Colony-Forming Units Assay, Flow Cytometry, Genetic Vectors, Genotype, Granulocytes, Hematopoietic Stem Cells, Mice, Inbred C57BL, Mice, Transgenic, Proto-Oncogene Proteins, Blotting, Western, Trans-Activators, DNA Primers, Reverse Transcriptase Polymerase Chain Reaction, Myeloid Cells, Green Fluorescent Proteins, Mice

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