Brain research · 2017
A constitutively-active IKK-complex at the axon initial segment.
СтатьяНазвание и аннотация: Перевод в очереди
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König Hans-Georg, Watters Orla, Kinsella Sinéad, Ameen Mohammed, Fenner Beau J, Prehn Jochen H M
Аннотация
BACKGROUND: Previous studies provided evidence for an accumulation of IκB-kinase (IKK) α/β at the axon initial segment (AIS), a neuronal compartment defined by ankyrin-G expression. Here we explored whether the presence of the IKK-complex at the AIS was associated with the activation of IKK signaling at this site.
METHODS AND RESULTS: Proximity-ligation assays (PLAs) using pan-IKKα/β, phospho-IKKα/β-specific as well as ankyrin-G specific antibodies validated their binding to proximal epitopes in the AIS, while antibodies to other phosphorylated signaling proteins showed no preference for the AIS. Small-hairpin mediated silencing of IKKβ significantly reduced anti-phospho-IKKα/β-immunoreactivities in the AIS. ank3 gene-deficient cerebellar Purkinje cells also exhibited no phosphorylated IKKα/β at the proximal region of their axons. Transient ankyrin-G overexpression in PC12 cells augmented NF-κB transactivation in an ankyrin-G death-domain dependent manner. Finally, small molecule inhibitors of IKK-activity, including Aspirin, inhibited the accumulation of activated IKK proteins in the AIS.
CONCLUSION: Our data suggest the existence of a constitutively-active IKK signaling complex in the AIS.
METHODS AND RESULTS: Proximity-ligation assays (PLAs) using pan-IKKα/β, phospho-IKKα/β-specific as well as ankyrin-G specific antibodies validated their binding to proximal epitopes in the AIS, while antibodies to other phosphorylated signaling proteins showed no preference for the AIS. Small-hairpin mediated silencing of IKKβ significantly reduced anti-phospho-IKKα/β-immunoreactivities in the AIS. ank3 gene-deficient cerebellar Purkinje cells also exhibited no phosphorylated IKKα/β at the proximal region of their axons. Transient ankyrin-G overexpression in PC12 cells augmented NF-κB transactivation in an ankyrin-G death-domain dependent manner. Finally, small molecule inhibitors of IKK-activity, including Aspirin, inhibited the accumulation of activated IKK proteins in the AIS.
CONCLUSION: Our data suggest the existence of a constitutively-active IKK signaling complex in the AIS.
Предметные рубрики MeSH
AnimalsAnkyrinsAspirinAxon Initial SegmentCalbindinsCerebral CortexDose-Response Relationship, DrugEmbryo, MammalianEnzyme InhibitorsFlow CytometryGreen Fluorescent ProteinsI-kappa B KinaseI-kappa B ProteinsLigationMiceMice, Inbred C57BLNeuronsPhosphorylationRNA, Small InterferingRatsSerineSignal TransductionTime FactorsTransfection