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bioRxiv · 10.1101/2025.08.13.670133

NSF is required for diverse endocytic modes by promoting fusion and fission pore closure in secretory cells

Wu, X.-S.·Sun, T.·Shi, B.·Lee, S.·Zhang, Z.·Wei, L.·Wang, X.·Molakarimi, M.·Han, S.·Uy, A.·Gan, L.·Wu, L.-G.
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Abstract

The ATPase N-ethylmaleimide-sensitive factor (NSF), known for disassembling SNARE complexes, plays key roles in neurotransmitter release, neurotransmitter (AMPA, GABA, dopamine) receptor trafficking, and synaptic plasticity, and its dysfunction or mutation is linked to neurological disorders. These roles are largely attributed to SNARE-mediated exocytosis. Here, we reveal a previously unrecognized role for NSF: mediating diverse modes of endocytosis--including slow, fast, ultrafast, overshoot, and bulk--by driving closure of both fusion and fission pores. This function was consistently observed across large calyx nerve terminals, small hippocampal boutons, and chromaffin cells using capacitance recordings, synaptopHluorin imaging, electron microscopy, and multi-color pore-closure imaging. Results were robust across four NSF inhibitors, gene knockout, knockdown, and specific mutations. These findings establish NSF as a central regulator of membrane fission, kiss-and-run fusion, endocytosis, and exo-endocytosis coupling--offering new mechanistic insights into its diverse physiological and pathological roles in synaptic transmission, receptor trafficking, and neurological diseases.

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Wu, X.-S., Sun, T., Shi, B., Lee, S., Zhang, Z., Wei, L., Wang, X., Molakarimi, M., Han, S., Uy, A., Gan, L., Wu, L.-G.. 2025-08-18. NSF is required for diverse endocytic modes by promoting fusion and fission pore closure in secretory cells. https://doi.org/10.1101/2025.08.13.670133

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