- Title
- Actin- and dynamin-dependent maturation of bulk endocytosis restores neurotransmission following synaptic depletion
- Creator
- Nguyen, Tam H.; Maucort, Guillaume; Sullivan, Robert K. P.; Schenning, Mitja; Lavidis, Nickolas A.; McCluskey, Adam; Robinson, Phillip J.; Meunier, Frederic A.
- Relation
- ARC.DP0987669
- Relation
- PLoS One Vol. 7, Issue 5
- Publisher Link
- http://dx.doi.org/10.1371/journal.pone.0036913
- Publisher
- Public Library of Science
- Resource Type
- journal article
- Date
- 2012
- Description
- Bulk endocytosis contributes to the maintenance of neurotransmission at the amphibian neuromuscular junction by regenerating synaptic vesicles. How nerve terminals internalize adequate portions of the presynaptic membrane when bulk endocytosis is initiated before the end of a sustained stimulation is unknown. A maturation process, occurring at the end of the stimulation, is hypothesised to precisely restore the pools of synaptic vesicles. Using confocal time-lapse microscopy of FM1-43-labeled nerve terminals at the amphibian neuromuscular junction, we confirm that bulk endocytosis is initiated during a sustained tetanic stimulation and reveal that shortly after the end of the stimulation, nerve terminals undergo a maturation process. This includes a transient bulging of the plasma membrane, followed by the development of large intraterminal FM1-43-positive donut-like structures comprising large bulk membrane cisternae surrounded by recycling vesicles. The degree of bulging increased with stimulation frequency and the plasmalemma surface retrieved following the transient bulging correlated with the surface membrane internalized in bulk cisternae and recycling vesicles. Dyngo-4a, a potent dynamin inhibitor, did not block the initiation, but prevented the maturation of bulk endocytosis. In contrast, cytochalasin D, an inhibitor of actin polymerization, hindered both the initiation and maturation processes. Both inhibitors hampered the functional recovery of neurotransmission after synaptic depletion. Our data confirm that initiation of bulk endocytosis occurs during stimulation and demonstrates that a delayed maturation process controlled by actin and dynamin underpins the coupling between exocytosis and bulk endocytosis.
- Subject
- actins; cell membranes; endocytosis; vesicles
- Identifier
- http://hdl.handle.net/1959.13/1067113
- Identifier
- uon:18276
- Identifier
- ISSN:1932-6203
- Language
- eng
- Full Text
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