English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Disruption of adaptor protein 2μ (AP-2μ) in cochlear hair cells impairs vesicle reloading of synaptic release sites and hearing

Jung, S., Maritzen, T., Wichmann, C., Jing, Z., Neef, A., Revelo, N. H., et al. (2015). Disruption of adaptor protein 2μ (AP-2μ) in cochlear hair cells impairs vesicle reloading of synaptic release sites and hearing. EMBO Journal, 34(21), 2686-2702. doi:10.15252/embj.201591885.

Item is

Files

show Files

Locators

show
hide
Locator:
http://emboj.embopress.org/content/34/21/2686 (Publisher version)
Description:
-
OA-Status:

Creators

show
hide
 Creators:
Jung, SangYong, Author
Maritzen, Tanja, Author
Wichmann, Carolin, Author
Jing, ZhiZi, Author
Neef, Andreas1, Author           
Revelo, Natalia H, Author
Al-Moyed, Hanan, Author
Meese, Sandra, Author
Wojcik, Sonja M, Author
Panou, Iliana, Author
Bulut, Haydar, Author
Schu, Peter, Author
Ficner, Ralf, Author
Reisinger, Ellen, Author
Rizzoli, Silvio O, Author
Neef, Jakob, Author
Strenzke, Nicola, Author
Haucke, Volker, Author
Moser, Tobias, Author
Affiliations:
1Research Group Theoretical Neurophysics, Max Planck Institute for Dynamics and Self-Organization, Max Planck Society, ou_2063289              

Content

show
hide
Free keywords: active zone; endocytosis; release site clearance; synaptic ribbon; vesicle reformation
 Abstract: Active zones (AZs) of inner hair cells (IHCs) indefatigably release hundreds of vesicles per second, requiring each release site to reload vesicles at tens per second. Here, we report that the endocytic adaptor protein 2μ (AP-2μ) is required for release site replenishment and hearing. We show that hair cell-specific disruption of AP-2μ slows IHC exocytosis immediately after fusion of the readily releasable pool of vesicles, despite normal abundance of membrane-proximal vesicles and intact endocytic membrane retrieval. Sound-driven postsynaptic spiking was reduced in a use-dependent manner, and the altered interspike interval statistics suggested a slowed reloading of release sites. Sustained strong stimulation led to accumulation of endosome-like vacuoles, fewer clathrin-coated endocytic intermediates, and vesicle depletion of the membrane-distal synaptic ribbon in AP-2μ-deficient IHCs, indicating a further role of AP-2μ in clathrin-dependent vesicle reformation on a timescale of many seconds. Finally, we show that AP-2 sorts its IHC-cargo otoferlin. We propose that binding of AP-2 to otoferlin facilitates replenishment of release sites, for example, via speeding AZ clearance of exocytosed material, in addition to a role of AP-2 in synaptic vesicle reformation.

Details

show
hide
Language(s): eng - English
 Dates: 2015-10-072015-11-03
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: BibTex Citekey: JungMaritzenWichmannEtAl2015
DOI: 10.15252/embj.201591885
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: EMBO Journal
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 34 (21) Sequence Number: - Start / End Page: 2686 - 2702 Identifier: -