4.7 Article

Identification of regulatory functions for 4-1BB and 4-1BBL in myelopoiesis and the development of dendritic cells

Journal

NATURE IMMUNOLOGY
Volume 9, Issue 8, Pages 917-926

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ni.1632

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Funding

  1. NCI NIH HHS [CA85860, R01 CA085860] Funding Source: Medline
  2. NEI NIH HHS [EY013325, R01 EY013325] Funding Source: Medline
  3. NIAID NIH HHS [R01 AI059290, R01 AI042944-08, R01 AI042944, R01 AI042944-05A1, AI059290, R01 AI042944-06, R01 AI042944-07, R56 AI050265, R01 AI050265, AI050265, R01 AI042944-09, AI42944] Funding Source: Medline

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The costimulatory molecule 4-1BB and its ligand 4-1BBL can control adaptive immunity, but here we show that their interaction also suppressed myelopoiesis. We found that 4-1BBL was expressed on hematopoietic stem cells, differentiating common myeloid progenitors and granulocyte-macrophage progenitors, and 4-1BB was inducible on activated myeloid progenitors. Steady-state numbers of granulocyte-macrophage progenitors, myeloid-lineage cells and mature dendritic cells were higher in 4-1BB- and 4-1BBL-deficient mice, indicative of a negative function, and we confirmed that result with bone marrow chimeras and in vitro, where the absence of interactions between 4-1BB and 4-1BBL led to enhanced differentiation into dendritic cell lineages. The regulatory activity was mediated by 4-1BBL, with binding by 4-1BB inhibiting differentiation of myeloid progenitors. Thus, 4-1BB and 4-1BBL have a previously unknown function in limiting myelopoiesis and the development of dendritic cells.

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