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Stathmin Regulates Microtubule Dynamics and Microtubule Organizing Center Polarization in Activated T Cells
Author(s) -
Erin L. Filbert,
Marie Le Borgne,
Joseph Lin,
John E. Heuser,
Andréy S. Shaw
Publication year - 2012
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1200242
Subject(s) - stathmin , microtubule organizing center , microtubule , microbiology and biotechnology , immunological synapse , mapk/erk pathway , phosphorylation , dephosphorylation , biology , regulator , chemistry , cell , centrosome , t cell , cell cycle , biochemistry , immunology , immune system , t cell receptor , phosphatase , gene
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.

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