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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Citations
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Cited by:
- 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.
- 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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