Cutting Edge: Atypical PKCs Regulate T Lymphocyte Polarity and Scanning Behavior
Author(s) -
Eliana Real,
Sophie Faure,
Emmanuel Donnadieu,
Jérôme Delon
Publication year - 2007
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.179.9.5649
Subject(s) - microbiology and biotechnology , polarity (international relations) , motility , chemotaxis , cell polarity , biology , receptor , protein subunit , neuroscience , chemokine , cell , genetics , gene
Leukocyte locomotion is a polarized process with diverse regulatory assemblies segregating along an anterior-posterior axis that defines two regions within the cell, the leading edge and the uropod. However, the mechanisms that generate T cell asymmetry downstream of chemokine receptors are ill defined. In this study we show that the atypical protein kinases C (aPKCs), PKCiota and PKCzeta, are required for an early symmetry breaking step. Once the polarity is established, aPKCs also drive uropod formation. These effects depend on the interaction between Par6 and aPKCs. Finally, failure to transduce aPKC-dependent signals reduces T cell motility and their ability to scan dendritic cells. Altogether, our findings suggest that lymphocyte motor activity is regulated by a signaling cascade that relays chemokinetic input to aPKCs.
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