Phosphatidylinositol 3,5-bisphosphate facilitates axonal vesicle transport and presynapse assembly

Author:

Rizalar Filiz Sila1ORCID,Lucht Max T.1ORCID,Petzoldt Astrid2ORCID,Kong Shuhan1,Sun Jiachen3ORCID,Vines James H.4,Telugu Narasimha Swamy5ORCID,Diecke Sebastian5ORCID,Kaas Thomas6ORCID,Bullmann Torsten6ORCID,Schmied Christopher1ORCID,Löwe Delia1,King Jason S.4ORCID,Cho Wonhwa3,Hallermann Stefan6ORCID,Puchkov Dmytro1ORCID,Sigrist Stephan J.2ORCID,Haucke Volker127ORCID

Affiliation:

1. Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), 13125 Berlin, Germany.

2. Department of Biology, Chemistry, Pharmacy, Freie Universität Berlin, 14195 Berlin, Germany.

3. Department of Chemistry, University of Illinois Chicago, Chicago, IL 60607, USA.

4. School of Biosciences, University of Sheffield, Firth Court Western Bank, Sheffield S10 2TN, UK.

5. Max-Delbrück-Centrum für Molekulare Medizin (MDC), Technology Platform Pluripotent Stem Cells, 13125 Berlin, Germany.

6. Carl-Ludwig Institute of Physiology, Faculty of Medicine, Leipzig University, 04103 Leipzig, Germany.

7. NeuroCure Cluster of Excellence, Charité–Universitätsmedizin Berlin, 10117 Berlin, Germany.

Abstract

Neurons relay information via specialized presynaptic compartments for neurotransmission. Unlike conventional organelles, the specialized apparatus characterizing the neuronal presynapse must form de novo. How the components for presynaptic neurotransmission are transported and assembled is poorly understood. Our results show that the rare late endosomal signaling lipid phosphatidylinositol 3,5-bisphosphate [PI(3,5)P 2 ] directs the axonal cotransport of synaptic vesicle and active zone proteins in precursor vesicles in human neurons. Precursor vesicles are distinct from conventional secretory organelles, endosomes, and degradative lysosomes and are transported by coincident detection of PI(3,5)P 2 and active ARL8 via kinesin KIF1A to the presynaptic compartment. Our findings identify a crucial mechanism that mediates the delivery of synaptic vesicle and active zone proteins to developing synapses.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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