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Blood, 15 January 2007, Vol. 109, No. 2, pp. 643-652.
Prepublished online as a Blood First Edition Paper on September 12, 2006; DOI 10.1182/blood-2006-04-016840.
Previous Article | Next Article 
Submitted April 26, 2006
Accepted August 20, 2006
Differentiation of CD1a- and CD1a+ monocyte-derived dendritic cells is biased by lipid environment and PPAR
Peter Gogolak, Bence Rethi, Istvan Szatmari, Arpad Lanyi, Balazs Dezso, Laszlo Nagy, and Eva Rajnavolgyi*
Institute of Immunology, University of Debrecen, Debrecen, Hungary
Institute of Biochemistry and Molecular Biology, University of Debrecen, Debrecen, Hungary
Department of Pathology, University of Debrecen, Debrecen, Hungary
Department of Immunology, University of Debrecen, Debrecen, Hungary
* Corresponding author; email: evaraj{at}jaguar.unideb.hu.
Accumulating data have shown that the microenvironment of dendritic cells modulates subtype differentiation and CD1 expression, but the mechanisms by which exogenous factors confer these effects are poorly understood. Here we describe the dependence of monocyte-derived CD1a- dendritic cell (moDC) development on lipids associated with the expression of peroxisome proliferator-activated receptor-gamma (PPAR ). We also show the consecutive differentiation of immature CD1a-PPAR + moDCs to CD1a+PPAR - cells limited by serum lipoproteins and terminated by pro-inflammatory cytokines. Immature CD1a- moDCs possess higher internalizing capacity than CD1a+ cells while both activated subtypes have similar migratory potential but differ in their cytokine and chemokine profiles that translates to distinct T-lymphocyte polarizing capacities. CD1a+ moDCs stand out by their capability to secrete high amounts of IL-12p70 and CCL1. As lipoproteins skew moDC differentiation toward the generation of CD1a-PPAR + cells and inhibit the development of CD1a+PPAR - cells we suggest that the uptake of lipids results in endogenous PPAR agonists that induce a cascade of gene transcription coordinating lipid metabolism, the expression of lipid presenting CD1 molecules, subtype dichotomy and function. The presence of CD1a-PPAR + and CD1a+PPAR - DCs in lymph nodes and in pulmonary Langerhans cell histiocytosis confirms the functional relevance of these DC subsets in vivo.

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