A novel role of toll-like receptor (TLR)-9 in synaptic plasticity and efficacy is proposed.
Nerve stimulation of TLR9 KO muscles produced weaker force compared to wild type.
NMJs, studied as a model synapse, showed pre-synaptic and post-synaptic defects in TLR9 KO mice.
Presynaptic defects included abnormal spontaneous and evoked vesicle release.
Endplate volume, as measured by α-bungarotoxin staining, declined.