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Endosomal phosphatidylinositol 3-phosphate controls synaptic vesicle cycling and neurotransmission

Liu, Guan‐Ting, Kochlamazashvili, Gaga, Puchkov, Dmytro, Müller, Rainer, Schultz, Carsten, Mackintosh, Albert I, Vollweiter, Dennis, Haucke, Volker, Soykan, Tolga·2022·The EMBO Journal
DOI 10.15252/embj.2021109352PMC PMC9058544
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Abstract

Neural circuit function requires mechanisms for controlling neurotransmitter release and the activity of neuronal networks, including modulation by synaptic contacts, synaptic plasticity, and homeostatic scaling. However, how neurons intrinsically monitor and feedback control presynaptic neurotransmitter release and synaptic vesicle (SV) recycling to restrict neuronal network activity remains poorly understood at the molecular level. Here, we investigated the reciprocal interplay between neuronal endosomes, organelles of central importance for the function of synapses, and synaptic activity. We show that elevated neuronal activity represses the synthesis of endosomal lipid phosphatidylinositol 3‐phosphate [PI(3)P] by the lipid kinase VPS34. Neuronal activity in turn is regulated by endosomal PI(3)P, the depletion of which reduces neurotransmission as a consequence of perturbed SV endocytosis. We find that this mechanism involves Calpain 2‐mediated hyperactivation of Cdk5 downstream of receptor‐ and activity‐dependent calcium influx. Our results unravel an unexpected function for PI(3)P‐containing neuronal endosomes in the control of presynaptic vesicle cycling and neurotransmission, which may explain the involvement of the PI(3)P‐producing VPS34 kinase in neurological disease and neurodegeneration.

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Metadata

Authors
Liu, G., Kochlamazashvili, G., Puchkov, D., Müller, R., Schultz, C., Mackintosh, A. I., Vollweiter, D., Haucke, V., & Soykan, T.
ORCID
Venue
The EMBO Journal
Publisher
Springer Science and Business Media LLC
Published
2022-03-22
Volume
41
Issue
9
ISSN
  • 0261-4189
  • 1460-2075
DOI
10.15252/embj.2021109352
PMC
PMC9058544
Cited by
19
References
8
Language
en
Licence
Funders
Deutsche Forschungsgemeinschaft (HA2686/13‐1, TRR186/ A09, EXC‐2049)

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