Journal
BLOOD
Volume 115, Issue 2, Pages 238-246Publisher
AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2009-08-236935
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Funding
- Oklahoma Center for the Advancement of Science Technology [HR06-157, AR081-006]
- National Institutes of Health [AI079616, RR020143, RR015577, RR16478]
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During inflammation, elevated granulocyte macrophage-colony-stimulating factor (GM-CSF) directs the development of new dendritic cells (DCs). This pathway is influenced by environmental factors, and we previously showed that physiologic levels of estradiol, acting through estrogen receptor alpha (ER alpha), promote the GM-CSF-mediated differentiation of a CD11b(+) DC subset from myeloid progenitors (MPs). We now have identified interferon regulatory factor 4 (IRF4), a transcription factor induced by GM-CSF and critical for CD11b(+) DC development in vivo, as a target of ER alpha signaling during this process. In MPs, ER alpha potentiates and sustains GM-CSF induction of IRF4. Furthermore, retroviral delivery of the Irf4 cDNA to undifferentiated ER alpha(-/-) bone marrow cells restored the development of the estradiol/ER alpha-dependent DC population, indicating that an elevated amount of IRF4 protein substitutes for ER alpha signaling. Thus at an early stage in the MP response to GM-CSF, ER alpha signaling induces an elevated amount of IRF4, which leads to a developmental program underlying CD11b(+) DC differentiation. (Blood. 2010; 115:238-246)
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