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  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.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0029-01D7-F Version Permalink: http://hdl.handle.net/11858/00-001M-0000-002A-22E9-3
Genre: Journal Article

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 Creators:
Jung, S., Author              
Maritzen, T., Author
Wichmann, C., Author
Jing, Z., Author
Neef, A., Author
Revelo, N. H., Author
Al‐Moyed, H., Author
Meese, S., Author
Wojcik, S. M., Author
Panou, I., Author
Bulut, H., Author
Schu, P., Author
Ficner, R., Author
Reisinger, E., Author
Rizzoli, S. O., Author
Neef, J., Author              
Strenzke, N., Author
Haucke, V., Author
Moser, T.1, Author              
Affiliations:
1Research Group of Synaptic Nanophysiology, MPI for Biophysical Chemistry, Max Planck Society, ou_2205655              

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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.

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Language(s): eng - English
 Dates: 2015-10-072015-11-03
 Publication Status: Published in print
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 Table of Contents: -
 Rev. Method: Peer
 Identifiers: DOI: 10.15252/embj.201591885
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Title: EMBO Journal
Source Genre: Journal
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Pages: - Volume / Issue: 34 (21) Sequence Number: - Start / End Page: 2686 - 2702 Identifier: -