ToxSci Advance Access published online on October 4, 2009
Toxicological Sciences, doi:10.1093/toxsci/kfp239
Differential impact of diesel particle composition on pro-allergic dendritic cell function




* ZAUM - Center for Allergy and Environment, Technische Universität München (TUM), Division of Environmental Dermatology and Allergy, Helmholtz Zentrum München/TUM, 80802 Munich, Germany
Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Ecological Chemistry, 85764 Neuherberg, Germany
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 |
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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