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ToxSci Advance Access published online on October 4, 2009

Toxicological Sciences, doi:10.1093/toxsci/kfp239
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© The Author 2009. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org

Differential impact of diesel particle composition on pro-allergic dendritic cell function

Andrea Braun*, Mayte Bewersdorff*, Jutta Lintelmann{dagger}, Georg Matuschek{dagger}, Thilo Jakob{ddagger}, Martin Göttlicher§, Wolfgang Schober*, Jeroen T. M. Buters*, Heidrun Behrendt* and Martin Mempel*

* ZAUM - Center for Allergy and Environment, Technische Universität München (TUM), Division of Environmental Dermatology and Allergy, Helmholtz Zentrum München/TUM, 80802 Munich, Germany {dagger} Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Ecological Chemistry, 85764 Neuherberg, Germany {ddagger} Allergy Research Group, Department of Dermatology, University Medical Center Freiburg, 79104 Freiburg, Germany § Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Toxicology, 85764 Neuherberg, Germany Department of Dermatology and Allergy Biederstein, Technische Universität München, 80802 Munich, Germany

Corresponding author: Martin Mempel, Helmholtz Zentrum München, Division of Environmental Dermatology and Allergy, Building 34, Room 230, Ingolstädter Landstraße 1, 85764 Neuherberg, Phone: +49/89/3187/2556, Fax: +49/89/3187/2540, e-mail address: martin.mempel{at}lrz.tu-muenchen.de

Received June 18, 2009; revision received September 2, 2009; accepted September 15, 2009


   Abstract

Diesel exhaust particles (DEP) were described as potent adjuvant in the induction and maintenance of allergic diseases suggesting that they might play a role in the increase of allergic diseases in the industrialized countries. However, the cellular basis by which these particles enhance allergic immune responses is still a matter of debate.

Thus, we exposed immature murine bone marrow-derived dendritic cells (BMDC) to different particles or particle-associated organic compounds in the absence or presence of the maturation stimuli lipopolysachharide and analyzed the cellular maturation, viability, and cytokine production. Furthermore, we monitored the functionality of particle-exposed BMDC to suppress B cell isotype switching to IgE.

Only highly polluted DEP (standard reference material SRM1650a) but not particle-associated organic compounds or less polluted DEP from modern diesel engines were able to modulate the dendritic cell phenotype. SRM1650a particles significantly suppressed LPS-induced IL-12p70 production in murine BMDC, whereas cell surface marker expression was not altered. Furthermore, SRM1650a-exposed immature BMDC lost the ability to suppress IgE isotype switch in B cells.

This study revealed that highly polluted DEP not only interfere with dendritic cell maturation but additionally with dendritic cell function, thus suggesting a role in Th2 immune deviation.

Key Words: Dendritic cells; B cells; IgE; particles; organic compounds.


e-mail addresses: andrea.braun{at}helmholtz-muenchen.de, mayte.b{at}gmx.de, matuschek{at}helmholtz-muenchen.de, thilo.jakob{at}uniklinik-freiburg.de, martin.goettlicher{at}helmholtz-muenchen.de, wolfgang.schober{at}lrz.tu-muenchen.de, buters{at}lrz.tum.de, heidrun.behrendt{at}lrz.tum.de, martin.mempel{at}lrz.tu-muenchen.de


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