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. 2016 Feb 4;7:24. doi: 10.3389/fimmu.2016.00024

Table 3.

Molecular determinants of PKC-θ localization at the immunological synapse.

Interaction/activity Molecular determinants Effect on immunological synapse Reference
PKC-θ–CD28 Polyproline motif within the PKC-θ V3 hinge region and PYAP motif in CD28; Lck-mediated interaction PKC-θ V3 hinge and CD28 PYAP motif are required for CD28 cSMAC localization Kong et al. (124)
PKC-θ–CD28 Sumoylation of PKC-θ at lysines 325 and 506 Abrogated PKC-θ sumoylation reduces PKC-θ localization at the IS and its colocalization with CD28, induces colocalization of PKC-θ and filamin A at periphery of the IS Wang et al. (139)
PKC-θ–DAG C1 domains of PKC-θ C1 domains mediate initial PKC-θ recruitment to the synaptic membrane, but they do not support PKC-θ central accumulation at the synapse Basu et al. (134), Carrasco and Merida (136), Quann et al. (135)
PKC-θ kinase activity Unknown, possibly through autophosphorylation at threonine 219 between the tandem C1 domains PKC-θ kinase activity is required for its recruitment to the IS Cartwright et al. (138), Thuille et al. (137)
Rltpr Unknown, no interaction between Rltpr and PKC-θ has been detected Wild-type Rltpr is required for PKC-θ and CARMA1 recruitment to cSMAC Liang et al. (113)