Litcius/Paper detail

Separation of presynaptic Ca <sub>v</sub> 2 and Ca <sub>v</sub> 1 channel function in synaptic vesicle exo- and endocytosis by the membrane anchored Ca <sup>2+</sup> pump PMCA

Niklas Krick, Stefanie Ryglewski, Aylin Pichler, Arthur Bikbaev, Torsten Götz, Oliver Kobler, Martin Heine, Ulrich Thomas, Carsten Duch

2021Proceedings of the National Academy of Sciences33 citationsDOIOpen Access PDF

Abstract

Significance Synaptic vesicle (SV) release from presynaptic terminals requires nanometer precise control of action potential (AP)–triggered calcium influx through voltage-gated calcium channels (VGCCs). SV recycling also depends on calcium signals, though in different spatiotemporal domains. Mechanisms for separate control of SV release and recycling by AP-triggered calcium influx remain elusive. Here, we demonstrate largely independent regulation of release and recycling by two different populations of VGCCs (Ca v 2, Ca v 1), identify Ca v 1 as one of potentially multiple calcium entry routes for endocytosis regulation, and show functional separation of simultaneous calcium signals in the nanometer space of a presynaptic terminal by the plasma membrane calcium ATPase (PMCA). The Ca v 2/Ca v 1/PMCA functional triad may provide conserved means for independent control of different vital presynaptic functions.

Topics & Concepts

Active zoneSynaptic vesicleNeurotransmitterCell biologyVoltage-dependent calcium channelBiologyNeuromuscular junctionNeurotransmissionAxonSynaptic vesicle recyclingNeuroscienceEndocytosisCalciumChemistryVesicleBiochemistryReceptorCentral nervous systemMembraneOrganic chemistryCellular transport and secretionLipid Membrane Structure and BehaviorNeurobiology and Insect Physiology Research