Immune complexes exposed on mast cell-derived nanovesicles amplify allergic inflammation

01 Pubblicazione su rivista
Molfetta Rosa, Lecce Mario, Quatrini Linda, Caracciolo Giulio, Digiacomo Luca, Masuelli Laura, Milito Nadia Domenica, Vulpis Elisabetta, Zingoni Alessandra, Galandrini Ricciarda, Santoni Angela, Paolini Rossella
ISSN: 1398-9995

Extracellular vesicles (EVs) are released by different cell types in- cluding mast cells (MCs) and are involved in intercellular communication thanks to their complex cargo of bioactive molecules. Among them, exosomes represent nanovesicles (<150 nm) secreted from endosomal compartments upon their fusion with the plasma membrane. Through both constitutive and induced exocytosis, MCs release exosomes that deliver several molecules including mRNA/miRNA and subunits of the high-affinity IgE receptor (Fc?RI). However, the role of MC-derived vesicles in the context of allergic reactions is still controversial. A recent study provides evidence that exosomes re- leased from unstimulated mouse bone marrow-derived mast cells (mBMMCs) bind to free IgE and decrease circulating IgE levels, thus inhibiting the allergic response. In contrast, several evidences support a positive regulatory role of MC-derived exosomes, suggesting that depending on MC activation status they can either attenuate or stimulate the inflammatory responses.

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