Klatt O, Repetto D, Brockhaus J, Reissner C, El Khallouqi A, Rohlmann A, Heine M, Missler M
Forschungsartikel (Zeitschrift) | Peer reviewedNeurexins are key organizer molecules that regulate synaptic function and are implicated in autism and schizophrenia. beta-neurexins interact with numerous cell adhesion and receptor molecules, but their neuronal localization remains elusive. Using single-molecule tracking and high-resolution microscopy to detect neurexin1 beta and neurexin3 beta in primary hippocampal neurons from knockin mice, we demonstrate that endogenous beta-neurexins are present in fewer than half of excitatory and inhibitory synapses. Moreover, we observe a large extrasynaptic pool of beta-neurexins on axons and show that axonal beta-neurexins diffuse with higher surface mobility than those transiently confined within synapses. Stimulation of neuronal activity further increases the mobility of synaptic and axonal beta-neurexins, whereas inhibition causes the opposite. Blocking ectodomain cleavage by metalloproteases also reduces beta-neurexin mobility and enhances glutamate release. These findings suggest that the surface mobility of endogenous beta-neurexins inside and outside of synapses is dynamically regulated and linked to neuronal activity.
Brockhaus, Johannes Ulrich | Institut für Anatomie und Molekulare Neurobiologie |
Missler, Markus | Institut für Anatomie und Molekulare Neurobiologie |
Reißner, Carsten Volker | Institut für Anatomie und Molekulare Neurobiologie |