WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

The Journal of Neuroscience, June 17, 2009, 29(24):7706-7717; doi:10.1523/JNEUROSCI.1976-09.2009

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Data
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (1)
Google Scholar
Right arrow Articles by Clayton, E. L.
Right arrow Articles by Cousin, M. A.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Clayton, E. L.
Right arrow Articles by Cousin, M. A.

 Previous Article  |  Next Article 

Cellular/Molecular
The Phospho-Dependent Dynamin–Syndapin Interaction Triggers Activity-Dependent Bulk Endocytosis of Synaptic Vesicles

Emma L. Clayton,1 Victor Anggono,2 Karen J. Smillie,1 Ngoc Chau,2 Phillip J. Robinson,2 and Michael A. Cousin1

1Membrane Biology Group, Centre for Integrative Physiology, George Square, University of Edinburgh, Edinburgh EH8 9XD, United Kingdom, and 2Children's Medical Research Institute, The University of Sydney, Wentworthville 2145, New South Wales, Australia

Correspondence should be addressed to Michael A. Cousin, Membrane Biology Group, Centre for Integrative Physiology, George Square, University of Edinburgh, Edinburgh EH8 9XD, UK. Email: m.cousin{at}ed.ac.uk

Synaptic vesicles (SVs) are retrieved by more than one mode in central nerve terminals. During mild stimulation, the dominant SV retrieval pathway is classical clathrin-mediated endocytosis (CME). During elevated neuronal activity, activity-dependent bulk endocytosis (ADBE) predominates, which requires activation of the calcium-dependent protein phosphatase calcineurin. We now report that calcineurin dephosphorylates dynamin I in nerve terminals only above the same activity threshold that triggers ADBE. ADBE was arrested when the two major phospho-sites on dynamin I were perturbed, suggesting that dynamin I dephosphorylation is a key step in its activation. Dynamin I dephosphorylation stimulates a specific dynamin I–syndapin I interaction. Inhibition of this interaction by competitive peptides or by site-directed mutagenesis exclusively inhibited ADBE but did not affect CME. The results reveal that the phospho-dependent dynamin–syndapin interaction recruits ADBE to massively increase SV endocytosis under conditions of elevated neuronal activity.


Received April 27, 2009; accepted May 15, 2009.

Correspondence should be addressed to Michael A. Cousin, Membrane Biology Group, Centre for Integrative Physiology, George Square, University of Edinburgh, Edinburgh EH8 9XD, UK. Email: m.cousin{at}ed.ac.uk




This article has been cited by other articles:


Home page
J. Neurosci.Home page
M. A. Gaffield, L. Tabares, and W. J. Betz
Preferred Sites of Exocytosis and Endocytosis Colocalize during High- But Not Lower-Frequency Stimulation in Mouse Motor Nerve Terminals
J. Neurosci., December 2, 2009; 29(48): 15308 - 15316.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-