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GTP-independent rapid and slow endocytosis at a central synapse

  • Jianhua Xu
    ,
  • Benjamin McNeil
    ,
  • Wei Wu
    ,
  • David Nees
    ,
  • Li Bai
    ,
  • Ling Gang Wu(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Vesicle endocytosis is essential for maintaining synaptic transmission. Its key step, membrane scission, is thought to be mediated by the GTPase dynamin in all forms of endocytosis at synapses. Our findings indicate that GTP-independent and probably dynamin-independent endocytosis co-exist with GTP- and dynamin-dependent endocytosis at the same synaptic nerve terminal, the calyx of Held, in rats. This previously undescribed form of endocytosis could be slow (tens of seconds) and/or rapid (a few seconds), similar to GTP- and dynamin-dependent endocytosis. It was activated during intense stimulation, whereas GTP- and dynamin-dependent endocytosis dominated during mild stimulation. These results establish a new model, in which vesicles are divided into two pools depending on their requirement for GTP and dynamin for retrieval. The GTP- and dynamin-dependent pool has higher priority for release and retrieval, but limited capacity, saturation of which leads to release and thus retrieval of GTP- and dynamin-independent vesicles.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 45-53 (9 pages)

Journal (Volume, Issue Number)

Nature Neuroscience (Volume 11, Issue 1)

Publication milestones

  • Published - 01/2008

Publication status

Published - 01/2008

ISSN

1097-6256

Publication IDs

  • Scopus: 37549055011
  • PubMed: 18066059

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
1.67
SciVal
Author count
6
SciVal
citations
60
SciVal
Paper percentile
91
SciVal
Top percentile
10
Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1

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Citation count
78
Captures
88

Funding Details

This work was supported by the National Institute of Neurological Disorders and Stroke Intramural Research Program.
FunderFunding numbers
NINDS
-