Cited by 432T-cell and B-cell ImmunologyHematopoietic Stem Cell TransplantationDevelopmental Biology and Gene Regulation

Heterogeneity among DN1 prothymocytes reveals multiple progenitors with different capacities to generate T cell and non-T cell lineages.

Open access
Porritt, Helen E, Rumfelt, Lynn L, Tabrizifard, Sahba, Schmitt, Thomas M, Zúñiga-Pflücker, Juan Carlos, Petrie, Howard T·2004·Immunity

Abstract

The nature of early T lineage progenitors in the thymus or bone marrow remains controversial. Here we assess lineage capacity and proliferative potential among five distinct components of the earliest intrathymic stage (DN1, CD25(-)44(+)). All of these express one or more hemato-lymphoid lineage markers. All can produce T lineage cells, but only two of them display kinetics of differentiation, proliferative capacity, and other traits consistent with being canonical T progenitors. The latter also appeared limited to producing cells of the T or NK lineages, while B lineage potential derived mainly from the other, less typical T progenitors. In addition to precisely defining canonical early progenitors in the thymus, this work reconciles conflicting results from numerous groups by showing that multiple progenitors with a DN1 phenotype home to the thymus and make T cells, but possess different proliferative potentials and lineage capacities.

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Crossref · 10.1016/j.immuni.2004.05.004

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  • Both αβ and γδ T cells arise from common multipotent DN precursors in the thymus.

    “Both αβ and γδ T cells arise from common multipotent DN precursors in the thymus that can be further separated into four DN subsets based on CD44 and CD25 expression [2], [3].”

    From The Transcription Factor PU.1 Regulates γδ T Cell Homeostasis (2011) · cites this paper as [2]

    The Results and Discussion (page numbers unavailable) identify DN1a and DN1b as early thymic T-cell progenitors, and the Results report that they can also generate cells expressing an NK-lineage marker. Our copy does not establish that both αβ and γδ T cells arise from a common DN precursor; the paper discusses T-lineage output without demonstrating that shared origin. (LLM, conf=0.82)

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Research works printed but not linked: 8

  1. [3]3. Bhandoola, A ∙ Sambandam, A ∙ Allman, D ... Early T lineage progenitorsnew insights, but old questions remain J. Immunol. 2003; 171:5653-5658 PubMed Google Scholar
  2. [4]4. Carlyle, J.R ∙ Zúñiga-Pflücker, J.C Requirement for the thymus in alphabeta T lymphocyte lineage commitment Immunity. 1998; 9:187-197 Full Text Full Text (PDF) Scopus (87) PubMed Google Scholar
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Authors
Porritt, H. E., Rumfelt, L. L., Tabrizifard, S., Schmitt, T. M., Zúñiga-Pflücker, J. C., & Petrie, H. T.
Affiliations
  • University of Miami (US)
  • Sunnybrook Health Science Centre (CA)
  • University of Toronto (CA)
Corresponding author
Petrie, Howard T
Venue
Immunity
Publisher
Elsevier BV
Published
2004-06
Volume
20
Issue
6
Pages
735-745
ISSN
1074-7613 (ISSN-L)
OpenAlex
W1981611424
Cited by
432
References
3
Citations by year
2026: 5 · 2025: 9 · 2024: 7 · 2023: 8 · 2022: 10 · 2021: 9 · 2020: 17 · 2019: 15 · 2018: 17 · 2017: 12 · 2016: 15 · 2015: 13 · 2014: 13 · 2013: 21 · 2012: 16
FWCI
16.50
Type
journal article
Language
en
Open access
Locations
  • Immunity (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institute of Allergy and Infectious Diseases (AI53739, R21AI053739, AI 33940)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Health Sciences › Medicine › Hematology › Hematopoietic Stem Cell Transplantation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
Keywords
T cell lineage commitment, NK cell lineage, B-cell lineage, proliferative capacity, thymus, bone marrow
MeSH terms
Animals, Cell Differentiation, Cell Division, Cell Movement, Cells, Cultured, Flow Cytometry, Mice, Inbred C57BL, Stem Cells, Thymus Gland, Antigens, CD, T-Lymphocyte Subsets, Cell Lineage, Mice

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