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Blood, 15 November 2005, Vol. 106, No. 10, pp. 3457-3464.
Prepublished online as a Blood First Edition Paper on July 21, 2005; DOI 10.1182/blood-2004-12-4965.
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Submitted January 3, 2005
Accepted July 8, 2005
Distinct roles for the NF- B1 and c-Rel transcription factors in the differentiation and survival of plasmacytoid and conventional dendritic cells activated by TLR-9 signals
Meredith O'Keeffe, Raelene J Grumont, Hubertus Hochrein, Martina Fuchsberger, Raffi Gugasyan, David Vremec, Ken Shortman, and Steve Gerondakis*
The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
Department of Medical Microbiology, Immunology and Hygeine, Technische Univesitat Muchen Trogstrs, Muchen, Germany
* Corresponding author; email: gerondakis{at}wehi.edu.au.
Rel/NF- B activation is a ubiquitous outcome of engaging Toll like receptors (TLR), yet the cell-type specific functions of this pathway in response to particular microbial signals remain poorly defined. Here we show that NF- B1 and c-Rel, Rel/NF- B proteins induced in conventional (cDC) and plasmacytoid (pDC) dendritic cells by CpG DNA, a TLR-9 ligand, serve markedly different functions in these DC subsets. With the exception of impaired IL-12 production, cultured nfkb1-/-c-rel-/- cDC responded relatively normally to CpG DNA. In contrast, CpG treated nfkb1-/-c-rel-/- pDC which were still able to produce type I interferon and Rantes, but not IL-6 or IL-12, failed to acquire an activated dendritic phenotype and underwent apoptosis. Although the TLR-9 mediated death of nfkb1-/-c-rel-/- pDC, which coincided with a failure to upregulate the prosurvival proteins Bcl-xL and A1 was blocked by Bcl-2 transgene expression, this inhibition of apoptosis still failed to rescue the differentiation defects. This indicated that these NF- B transcription factors independently regulate TLR-9 mediated pDC morphogenesis and survival. Collectively, these findings establish that NF- B1 and c-Rel whilst largely dispensable for TLR-9 induced cDC activation, are critical for regulating differentiation and survival programs during pDC activation.

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