http://www.cnr.it/ontology/cnr/individuo/prodotto/ID292159
Diesel exhaust particle exposure in vitro impacts T lymphocyte phenotype and function (Articolo in rivista)
- Type
- Label
- Diesel exhaust particle exposure in vitro impacts T lymphocyte phenotype and function (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1186/s12989-014-0074-0 (literal)
- Alternative label
Marina Pierdominici, Angela Maselli, Serena Cecchetti, Antonella Tinari, Arianna Mastrofrancesco, Michela Alfè, Valentina Gargiulo, Carlo Beatrice, Gabriele Di Blasio, Giulia Carpinelli, Elena Ortona, Antonello Giovannetti, Silvana Fiorito (2014)
Diesel exhaust particle exposure in vitro impacts T lymphocyte phenotype and function
in Particle and fibre toxicology
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Marina Pierdominici, Angela Maselli, Serena Cecchetti, Antonella Tinari, Arianna Mastrofrancesco, Michela Alfè, Valentina Gargiulo, Carlo Beatrice, Gabriele Di Blasio, Giulia Carpinelli, Elena Ortona, Antonello Giovannetti, Silvana Fiorito (literal)
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- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
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- Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Rome, Italy
Department of Technology and Health, Istituto Superiore di Sanità, Rome, Italy
San Gallicano Dermatologic Institute, IRCCS-IFO, Laboratory of Cutaneous Physiopathology and Integrated Center of Metabolomics Research, Rome, Italy
Istituto di Ricerche sulla Combustione (IRC), CNR- Naples, Italy
Istituto Motori (IM), CNR-Naples, Italy
Istituto San Raffaele Sulmona, Sulmona, Italy
Department of Clinical Medicine, Division of Clinical Immunology, Sapienza, University of Rome, Rome, Italy
Institute of Translational Pharmacology, CNR-Rome, Italy
Research Center for Nanotechnologies applied to Engineering-CNIS, Rome, Italy
Department of Clinical Medicine, Division of Clinical Immunology, Sapienza University of Rome, Rome, Italy (literal)
- Titolo
- Diesel exhaust particle exposure in vitro impacts T lymphocyte phenotype and function (literal)
- Abstract
- Background
Diesel exhaust particles (DEP) are major constituents of ambient air pollution and their adverse health effect is an area of intensive investigations. With respect to the immune system, DEP have attracted significant research attention as a factor that could influence
allergic diseases interfering with cytokine production and chemokine expression. With this exception, scant data are available on the impact of DEP on lymphocyte homeostasis. Here, the effects of nanoparticles from Euro 4 (E4) and Euro 5 (E5) light duty diesel engines on the phenotype and function of T lymphocytes from healthy donors were evaluated.
Methods
T lymphocytes were isolated from peripheral blood obtained from healthy volunteers and subsequently stimulated with different concentration (from 0.15 to 60 µg/ml) and at different time points (from 24 h to 9 days) of either E4 or E5 particles. Immunological parameters, including apoptosis, autophagy, proliferation levels, mitochondrial function, expression of activation markers and cytokine production were evaluated by cellular and molecular analyses.
Results
DEP exposure caused a pronounced autophagic-lysosomal blockade, thus interfering with a key mechanism involved in the maintaining of T cell homeostasis. Moreover, DEP decreased mitochondrial membrane potential but, unexpectedly, this effect did not result in changes of the apoptosis and/or necrosis levels, as well as of intracellular content of adenosine triphosphate (ATP). Finally, a down-regulation of the expression of the alpha chain of the interleukin (IL)-2 receptor (i.e., the CD25 molecule) as well as an abnormal Th1 cytokine expression profile (i.e., a decrease of IL-2 and interferon (IFN)-? production) were observed after DEP exposure. No differences between the two compounds were detected in all studied parameters.
Conclusions
Overall, our data identify functional and phenotypic T lymphocyte parameters as relevant targets for DEP cytotoxicity, whose impairment could be detrimental, at least in the long run, for human health, favouring the development or the progression of diseases such as autoimmunity and cancer. (literal)
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