TY - JOUR
T1 - Post-fusion structural changes and their roles in exocytosis and endocytosis of dense-core vesicles
AU - Chiang, Hsueh Cheng
AU - Shin, Wonchul
AU - Zhao, Wei Dong
AU - Hamid, Edaeni
AU - Sheng, Jiansong
AU - Baydyuk, Maryna
AU - Wen, Peter J.
AU - Jin, Albert
AU - Momboisse, Fanny
AU - Wu, Ling Gang
N1 - Funding Information:
We thank Dr. Fujun Luo for comments on the manuscript. We thank Drs. Carolyn Smith and Lei Xue for technical assistance in imaging. We thank Drs. Justin Taraska and Ronald Holz for providing NPY-EGFP and VAMP2-EGFP plasmids, respectively. This work was supported by the National Institute of Neurological Disorders and Stroke Intramural Research Program.
PY - 2014/2/24
Y1 - 2014/2/24
N2 - 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.
AB - 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.
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U2 - 10.1038/ncomms4356
DO - 10.1038/ncomms4356
M3 - Article
C2 - 24561832
AN - SCOPUS:84896896307
SN - 2041-1723
VL - 5
JO - Nature Communications
JF - Nature Communications
M1 - 3356
ER -