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Post-fusion structural changes and their roles in exocytosis and endocytosis of dense-core vesicles

Author

Listed:
  • Hsueh-Cheng Chiang

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012)

  • Wonchul Shin

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012)

  • Wei-Dong Zhao

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012)

  • Edaeni Hamid

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012)

  • Jiansong Sheng

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012)

  • Maryna Baydyuk

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012)

  • Peter J. Wen

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012)

  • Albert Jin

    (National Institute of Biomedical Imaging and Bioengineering (NIBIB))

  • Fanny Momboisse

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012
    Present address: Centro Interdisciplinario de Neurociencia de Valparaíso, Universidad de Valparaíso, Gran Bretaña 1111, Playa Ancha, Valparaíso 2360102, Chile)

  • Ling-Gang Wu

    (National Institute of Neurological Disorders and Stroke, 35 Convent Drive, Building 35, Room 2B-1012)

Abstract

Vesicle fusion with the plasma membrane generates an Ω-shaped membrane profile. Its pore is thought to dilate until flattening (full-collapse), followed by classical endocytosis to retrieve vesicles. Alternatively, the pore may close (kiss-and-run), but the triggering mechanisms and its endocytic roles remain poorly understood. Here, using confocal and stimulated emission depletion microscopy imaging of dense-core vesicles, we find that fusion-generated Ω-profiles may enlarge or shrink while maintaining vesicular membrane proteins. Closure of fusion-generated Ω-profiles, which produces various sizes of vesicles, is the dominant mechanism mediating rapid and slow endocytosis within ~1–30 s. Strong calcium influx triggers dynamin-mediated closure. Weak calcium influx does not promote closure, but facilitates the merging of Ω-profiles with the plasma membrane via shrinking rather than full-collapse. These results establish a model, termed Ω-exo–endocytosis, in which the fusion-generated Ω-profile may shrink to merge with the plasma membrane, change in size or change in size then close in response to calcium, which is the main mechanism to retrieve dense-core vesicles.

Suggested Citation

  • Hsueh-Cheng Chiang & Wonchul Shin & Wei-Dong Zhao & Edaeni Hamid & Jiansong Sheng & Maryna Baydyuk & Peter J. Wen & Albert Jin & Fanny Momboisse & Ling-Gang Wu, 2014. "Post-fusion structural changes and their roles in exocytosis and endocytosis of dense-core vesicles," Nature Communications, Nature, vol. 5(1), pages 1-17, May.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4356
    DOI: 10.1038/ncomms4356
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    Cited by:

    1. Wonchul Shin & Ben Zucker & Nidhi Kundu & Sung Hoon Lee & Bo Shi & Chung Yu Chan & Xiaoli Guo & Jonathan T. Harrison & Jaymie Moore Turechek & Jenny E. Hinshaw & Michael M. Kozlov & Ling-Gang Wu, 2022. "Molecular mechanics underlying flat-to-round membrane budding in live secretory cells," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
    2. Ling-Gang Wu & Chung Yu Chan, 2024. "Membrane transformations of fusion and budding," Nature Communications, Nature, vol. 15(1), pages 1-19, December.

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