Literature DB >> 27910998

Aurora-A shines on T cell activation through the regulation of Lck.

Noelia Blas-Rus1, Eugenio Bustos-Morán2, Noa B Martín-Cófreces2, Francisco Sánchez-Madrid1,2.   

Abstract

Different protein kinases control signaling emanating from the T cell receptor (TCR) during antigen-specific T cell activation. Mitotic kinases, e.g. Aurora-A, have been widely studied in the context of mitosis due to their role during microtubule (MT) nucleation, becoming critical regulators of cell cycle progression. We have recently described a specific role for Aurora-A kinase in antigenic T cell activation. Blockade of Aurora-A in T cells severely disrupts the dynamics of MTs and CD3ζ-bearing signaling vesicles during T cell activation. Furthermore, Aurora-A deletion impairs the activation of signaling molecules downstream of the TCR. Targeting Aurora-A disturbs the activation of Lck, which is one of the first signals that drive T cell activation in an antigen-dependent manner. This work describes possible models of regulation of Lck by Aurora-A during T cell activation. We also discuss possible roles for Aurora-A in other systems similar to the IS, and its putative functions in cell polarization.
© 2016 WILEY Periodicals, Inc.

Entities:  

Keywords:  Aurora-A kinase; Golgi apparatus; Lck tyrosine kinase; T cell activation; asymmetric cell division; immunological synapse; microvesicular traffic

Mesh:

Substances:

Year:  2016        PMID: 27910998      PMCID: PMC5268092          DOI: 10.1002/bies.201600156

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  54 in total

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Authors:  Noelia Blas-Rus; Eugenio Bustos-Morán; Ignacio Pérez de Castro; Guillermo de Cárcer; Aldo Borroto; Emilio Camafeita; Inmaculada Jorge; Jesús Vázquez; Balbino Alarcón; Marcos Malumbres; Noa B Martín-Cófreces; Francisco Sánchez-Madrid
Journal:  Nat Commun       Date:  2016-04-19       Impact factor: 14.919

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