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PMID: 16546084 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Altered synaptic development and active zone spacing in endocytosis mutants.

Current biology : CB ·Vol. 16 ·No. 6 ·2006-03-21 ·Pages 591-8

Dickman DK, Lu Z, Meinertzhagen IA, Schwarz TL

Abstract

Many types of synapses have highly characteristic shapes and tightly regulated distributions of active zones, parameters that are important to the function of neuronal circuits. The development of terminal arborizations must therefore include mechanisms to regulate the spacing of terminals, the frequency of branching, and the distribution and density of release sites. At present, however, the mechanisms that control these features remain obscure. Here, we report the development of supernumerary or "satellite" boutons in a variety of endocytic mutants at the Drosophila neuromuscular junction. Mutants in endophilin, synaptojanin, dynamin, AP180, and synaptotagmin all show increases in supernumerary bouton structures. These satellite boutons contain releasable vesicles and normal complements of synaptic proteins that are correctly localized within terminals. Interestingly, however, synaptojanin terminals have more active zones per unit of surface area and more dense bodies (T-bars) within these active zones, which may in part compensate for reduced transmission per active zone. The altered structural development of the synapse is selectively encountered in endocytosis mutants and is not observed when synaptic transmission is reduced by mutations in glutamate receptors or when synaptic transmission is blocked by tetanus toxin. We propose that endocytosis plays a critical role in sculpting the structure of synapses, perhaps through the endocytosis of unknown regulatory signals that organize morphogenesis at synaptic terminals.

MeSH Terms
Acyltransferases/genetics Animals Drosophila/genetics,growth & development,ultrastructure Drosophila Proteins/genetics Dynamins/genetics Endocytosis/genetics,physiology Image Processing, Computer-Assisted Larva/genetics,growth & development,ultrastructure Microscopy, Electron, Scanning Monomeric Clathrin Assembly Proteins/genetics Mutation Nerve Tissue Proteins/genetics Neuromuscular Junction/growth & development,ultrastructure Phenotype Phosphoric Monoester Hydrolases/genetics Presynaptic Terminals/metabolism,physiology,ultrastructure
Chemicals
Drosophila Proteins Monomeric Clathrin Assembly Proteins Nerve Tissue Proteins clathrin assembly protein AP180 Acyltransferases endophilin A, Drosophila synaptojanin Phosphoric Monoester Hydrolases Dynamins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Dickman Dion K
Division of Neuroscience, Children's Hospital, Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Lu Zhiyuan
Meinertzhagen Ian A
Schwarz Thomas L
Article Info
Journal
Current biology : CB
Abbr.
Curr Biol
ISSN
0960-9822
Published
2006-03-21
Pages
591-8
Language
English
Region
England
NLM ID
9107782
Subset
IM
Grants
NEI NIH HHS · EY-03592 · United States
NINDS NIH HHS · NS-14062 · United States
Corrections
ErratumIn
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