Adhesion shapes T cells for prompt and sustained T-cell receptor signalling

Rita Lucia Contento, Silvia Campello, Anna Elisa Trovato, Elena Magrini, Fabio Anselmi, Antonella Viola

Research output: Contribution to journalArticlepeer-review


During T-cell migration, cell polarity is orchestrated by chemokine receptors and adhesion molecules and involves the functional redistribution of molecules and organelles towards specific cell compartments. In contrast, it is generally believed that the cell polarity established when T cells meet antigen-presenting cells (APCs) is controlled by the triggered T-cell receptor (TCR). Here, we show that, during activation of human T lymphocytes by APCs, chemokines and LFA-1 establish cell polarity independently of TCR triggering. Chemokine-induced LFA-1 activation results in fast recruitment of MTOC and mitochondria towards the potential APC, a process required to amplify TCR Ca 2+ signalling at the upcoming immunological synapse, to promote nuclear translocation of transcriptional factor NFATc2 and boost CD25 expression. Our data show that the initial adhesive signals delivered by chemokines and LFA-1 shape and prepare T cells for antigen recognition.

Original languageEnglish
Pages (from-to)4035-4047
Number of pages13
JournalEMBO Journal
Issue number23
Publication statusPublished - Dec 1 2010


  • immunological synapse
  • LFA-1
  • mitochondria
  • T-cell polarity

ASJC Scopus subject areas

  • Molecular Biology
  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Microbiology(all)
  • Neuroscience(all)


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