| First Author | Kong KF | Year | 2011 |
| Journal | Nat Immunol | Volume | 12 |
| Issue | 11 | Pages | 1105-12 |
| PubMed ID | 21964608 | Mgi Jnum | J:177663 |
| Mgi Id | MGI:5295803 | Doi | 10.1038/ni.2120 |
| Citation | Kong KF, et al. (2011) A motif in the V3 domain of the kinase PKC-theta determines its localization in the immunological synapse and functions in T cells via association with CD28. Nat Immunol 12(11):1105-12 |
| abstractText | Protein kinase C-theta (PKC-theta) translocates to the center of the immunological synapse, but the underlying mechanism and its importance in T cell activation are unknown. Here we found that the V3 domain of PKC-theta was necessary and sufficient for localization to the immunological synapse mediated by association with the coreceptor CD28 and dependent on the kinase Lck. We identified a conserved proline-rich motif in V3 required for association with CD28 and immunological synapse localization. We found association with CD28 to be essential for PKC-theta-mediated downstream signaling and the differentiation of T helper type 2 cells (T(H)2 cells) and interleukin 17-producing helper T cells (T(H)17 cells) but not of T helper type 1 cells (T(H)1 cells). Ectopic expression of V3 sequestered PKC-theta from the immunological synapse and interfered with its functions. Our results identify a unique mode of CD28 signaling, establish a molecular basis for the immunological synapse localization of PKC-theta and indicate V3-based 'decoys' may be therapeutic modalities for T cell-mediated inflammatory diseases. |
