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Scientists and Projects
Sergio Abrignani
Silvia Barabino
Giorgio Battaglia
Andrea Becchetti
Ettore Biagi
Giorgio Biasi
Andrea Biondi
Francesco Broccolo
Silvia Brunelli
Maurizio C. Capogrossi
Giorgio Cattoretti
Guido Cavaletti
Clementina Cocuzza
Marco Crimi
Carlo Ferrarese
Giuliana Ferrari
Alessandra Ferri
Gaetano Finocchiaro
Katharina Fleischhauer
Maria Foti
Alberto Froio
Carlo Gambacorti-Passerini
Paolo Ghia
Gabriella Giagnoni
Roberto Giovannoni
Josée Golay
Francesca Granucci
Martino Introna
Marialuisa Lavitrano
Marzia Maria Lecchi
Renato Mantegazza
Massimo Masserini
Raffaela Meneveri
Paolo Mingazzini
Giuseppe Miserocchi
Monica Moro
Rosario Musumeci
Silvia Kirsten Nicolis
Sergio Ottolenghi
Gianfranco Parati
Marco Parenti
Roberto A. Perego
Maurizio Pesce
Antonio Pesenti
Alberto Piperno
Giulio Pompilio
Maria Pia Protti
Eva Reali
Paola Ricciardi-Castagnoli
Ilaria Rivolta
Antonella Ronchi
Elena Irene Rugarli
Giulio Alfredo Sancini
Valeria Tiranti
Antonio Torsello
Angelo Vescovi
Ivan Zanoni
Antonio Zaza
Massimo Zeviani
Name: Francesca Granucci
E-mail: francesca.granucci@unimib.it
Department: Biotechnology and Biosciences - UNIMIB
Research Area(s): Host-pathogen interactions

Selected Research Projects

Dendritic cells in innate and adaptive immunity
Dendritic cells (DC) are a special type of leukocytes able to alert the immune system for the presence of infections. They are extremely versatile antigen presenting cells involved in the initiation of both innate and adaptive immunity, but also in the differentiation of regulatory T cells required for the maintenance of self-tolerance. The research activity of this group is focused on different aspects of dendritic cell functionality

Induction and maintenance of peripheral T cell tolerance
The immune system of vertebrate animals has the capacity to respond to perturbations (invading pathogens, stress signals) limiting self-tissue damage. Tolerance to tissue antigens is achieved through a combination of thymic and peripheral events that eliminate or inactivate potentially dangerous T cells. Several mechanisms have been proposed to explain the induction of tolerance in peripheral autoreactive T cells. Taking advantage of different transgenic and knock out mouse models the mechanisms through which dendritic cells induce T cell tolerance in peripheral lymphoid organs are investigated.

Intercellular and intracellular mechanisms of dendritic cell-mediated NK cell activation
Natural Killer (NK) cells exert a direct anti-tumor and anti-microbial effect and can influence the development of adaptive T cell responses. Activation of NK cells is regulated by accessory cells such as dendritic cells (DC). Following activation, NK cells accumulate at the lymph nodes draining the site of infection, the key place in which DC and NK cell interactions occur. Taking advantage of the two-photon intravital microscopy technology the capacity of activated NK cells to reach the draining lymph nodes is investigated together with the DC-derived signals necessary for NK cell priming in inflammatory conditions.

Signals induced by lipopolysaccharides through CD14
The vertebrate immune system has evolved to detect and control invasions of microorganisms. Such perturbations are perceived by cells of the innate immune system that express Pattern Recognition Receptors (PRRs). These receptors bind a number of microbial products collectively named Microbial Associated Molecular Patterns (MAMPs). Among PRRs, Toll Like Receptors (TLRs) and their co-receptors are the best characterized. The focus in on intracellular signals induced by smooth and rough lipolysaccharides through CD14, a well-characterized TLR co-receptor, in dendritic cells.

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