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10.1242/jcs.199042

http://scihub22266oqcxt.onion/10.1242/jcs.199042
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C5589067!5589067!28209780
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suck abstract from ncbi


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pmid28209780      J+Cell+Sci 2017 ; 130 (7): 1217-23
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  • Microtubule-associated protein-4 controls nanovesicle dynamics and T cell activation #MMPMID28209780
  • Bustos-Morán E; Blas-Rus N; Martin-Cófreces NB; Sánchez-Madrid F
  • J Cell Sci 2017[Apr]; 130 (7): 1217-23 PMID28209780show ga
  • The immune synapse (IS) is a specialized structure formed at the contact area between T lymphocytes and antigen-presenting cells (APCs) that is essential for the adaptive immune response. Proper T cell activation requires its polarization towards the APC, which is highly dependent on the tubulin cytoskeleton. Microtubule-associated protein-4 (MAP4) is a microtubule (MT)-stabilizing protein that controls MTs in physiological processes, such as cell division, migration, vesicular transport or primary cilia formation. In this study, we assessed the role of MAP4 in T cell activation. MAP4 decorates the pericentrosomal area and MTs of the T cell, and it is involved in MT detyrosination and stable assembly in response to T cell activation. In addition, MAP4 prompts the timely translocation of the MT-organizing center (MTOC) towards the IS and the dynamics of signaling nanovesicles that sustains T cell activation. However, MAP4 acts as a negative regulator of other T cell activation-related signals, including diacylglycerol (DAG) production and IL2 secretion. Our data indicate that MAP4 acts as a checkpoint molecule that balances positive and negative hallmarks of T cell activation.
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