| Literature DB >> 22529300 |
Erin L Filbert1, Marie Le Borgne, Joseph Lin, John E Heuser, Andrey S Shaw.
Abstract
Polarization of T cells involves reorientation of the microtubule organizing center (MTOC). Because activated ERK is localized at the immunological synapse, we investigated its role by showing that ERK activation is important for MTOC polarization. Suspecting that ERK phosphorylates a regulator of microtubules, we next focused on stathmin, a known ERK substrate. Our work indicates that during T cell activation, ERK is recruited to the synapse, allowing it to phosphorylate stathmin molecules near the immunological synapse. Supporting an important role of stathmin phosphorylation in T cell activation, we showed that T cell activation results in increased microtubule growth rate dependent on the presence of stathmin. The significance of this finding was demonstrated by results showing that CTLs from stathmin(-/-) mice displayed defective MTOC polarization and defective target cell cytolysis. These data implicate stathmin as a regulator of the microtubule network during T cell activation.Entities:
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Year: 2012 PMID: 22529300 PMCID: PMC3358357 DOI: 10.4049/jimmunol.1200242
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422