Literature DB >> 16507769

Mouse plasmacytoid dendritic cells derive exclusively from estrogen-resistant myeloid progenitors.

Benjamin C Harman1, Juli P Miller, Neda Nikbakht, Rachel Gerstein, David Allman.   

Abstract

Current models predict that mouse plasmacytoid dendritic cells (PDCs) derive from lymphoid progenitors. However, we show PDCs arise exclusively from common myeloid progenitors (CMPs) characterized by low-level expression of several lymphoid-associated genes, including a RAG2/GFP reporter transgene. This conclusion is supported by both adoptive transfer experiments and an estrogen treatment strategy that led to marked depletion of very early lymphoid progenitors without affecting RAG2/GFP(+) CMPs or the developmental kinetics, RAG-mediated recombinase activity, and cytokine production of PDCs. These data suggest that PDCs arise exclusively from early myeloid progenitors and that promiscuous low-level expression of lymphoid-associated genes is a general feature of PDC progenitors among CMPs.

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Year:  2006        PMID: 16507769      PMCID: PMC1895850          DOI: 10.1182/blood-2005-11-4545

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  47 in total

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2.  Identification of very early lymphoid precursors in bone marrow and their regulation by estrogen.

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4.  Dendritic cell potentials of early lymphoid and myeloid progenitors.

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Journal:  Blood       Date:  2001-06-01       Impact factor: 22.113

5.  Plasmacytoid dendritic cells of different origins have distinct characteristics and function: studies of lymphoid progenitors versus myeloid progenitors.

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  18 in total

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4.  9-O-acetyl sialic acid levels identify committed progenitors of plasmacytoid dendritic cells.

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Review 7.  Transcriptional regulation of early B cell development.

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8.  Transcription factor E2-2 is an essential and specific regulator of plasmacytoid dendritic cell development.

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Review 10.  Estrogen receptors regulate an inflammatory pathway of dendritic cell differentiation: mechanisms and implications for immunity.

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