Synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells.
To faithfully encode mechanosensory information, auditory/vestibular hair cells utilize graded synaptic vesicle (SV) release at specialized ribbon synapses. The molecular basis of SV release and consequent recycling of membrane in hair cells has not been fully explored. Here, we report that comet, a...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2009-05-01
|
Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC2673039?pdf=render |
id |
doaj-d14c533385b749409d41415ba26b86f5 |
---|---|
record_format |
Article |
spelling |
doaj-d14c533385b749409d41415ba26b86f52020-11-24T21:19:12ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042009-05-0155e100048010.1371/journal.pgen.1000480Synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells.Josef G TrapaniNikolaus ObholzerWeike MoSusan E BrockerhoffTeresa NicolsonTo faithfully encode mechanosensory information, auditory/vestibular hair cells utilize graded synaptic vesicle (SV) release at specialized ribbon synapses. The molecular basis of SV release and consequent recycling of membrane in hair cells has not been fully explored. Here, we report that comet, a gene identified in an ENU mutagenesis screen for zebrafish larvae with vestibular defects, encodes the lipid phosphatase Synaptojanin 1 (Synj1). Examination of mutant synj1 hair cells revealed basal blebbing near ribbons that was dependent on Cav1.3 calcium channel activity but not mechanotransduction. Synaptojanin has been previously implicated in SV recycling; therefore, we tested synaptic transmission at hair-cell synapses. Recordings of post-synaptic activity in synj1 mutants showed relatively normal spike rates when hair cells were mechanically stimulated for a short period of time at 20 Hz. In contrast, a sharp decline in the rate of firing occurred during prolonged stimulation at 20 Hz or stimulation at a higher frequency of 60 Hz. The decline in spike rate suggested that fewer vesicles were available for release. Consistent with this result, we observed that stimulated mutant hair cells had decreased numbers of tethered and reserve-pool vesicles in comparison to wild-type hair cells. Furthermore, stimulation at 60 Hz impaired phase locking of the postsynaptic activity to the mechanical stimulus. Following prolonged stimulation at 60 Hz, we also found that mutant synj1 hair cells displayed a striking delay in the recovery of spontaneous activity. Collectively, the data suggest that Synj1 is critical for retrieval of membrane in order to maintain the quantity, timing of fusion, and spontaneous release properties of SVs at hair-cell ribbon synapses.http://europepmc.org/articles/PMC2673039?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Josef G Trapani Nikolaus Obholzer Weike Mo Susan E Brockerhoff Teresa Nicolson |
spellingShingle |
Josef G Trapani Nikolaus Obholzer Weike Mo Susan E Brockerhoff Teresa Nicolson Synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells. PLoS Genetics |
author_facet |
Josef G Trapani Nikolaus Obholzer Weike Mo Susan E Brockerhoff Teresa Nicolson |
author_sort |
Josef G Trapani |
title |
Synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells. |
title_short |
Synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells. |
title_full |
Synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells. |
title_fullStr |
Synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells. |
title_full_unstemmed |
Synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells. |
title_sort |
synaptojanin1 is required for temporal fidelity of synaptic transmission in hair cells. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Genetics |
issn |
1553-7390 1553-7404 |
publishDate |
2009-05-01 |
description |
To faithfully encode mechanosensory information, auditory/vestibular hair cells utilize graded synaptic vesicle (SV) release at specialized ribbon synapses. The molecular basis of SV release and consequent recycling of membrane in hair cells has not been fully explored. Here, we report that comet, a gene identified in an ENU mutagenesis screen for zebrafish larvae with vestibular defects, encodes the lipid phosphatase Synaptojanin 1 (Synj1). Examination of mutant synj1 hair cells revealed basal blebbing near ribbons that was dependent on Cav1.3 calcium channel activity but not mechanotransduction. Synaptojanin has been previously implicated in SV recycling; therefore, we tested synaptic transmission at hair-cell synapses. Recordings of post-synaptic activity in synj1 mutants showed relatively normal spike rates when hair cells were mechanically stimulated for a short period of time at 20 Hz. In contrast, a sharp decline in the rate of firing occurred during prolonged stimulation at 20 Hz or stimulation at a higher frequency of 60 Hz. The decline in spike rate suggested that fewer vesicles were available for release. Consistent with this result, we observed that stimulated mutant hair cells had decreased numbers of tethered and reserve-pool vesicles in comparison to wild-type hair cells. Furthermore, stimulation at 60 Hz impaired phase locking of the postsynaptic activity to the mechanical stimulus. Following prolonged stimulation at 60 Hz, we also found that mutant synj1 hair cells displayed a striking delay in the recovery of spontaneous activity. Collectively, the data suggest that Synj1 is critical for retrieval of membrane in order to maintain the quantity, timing of fusion, and spontaneous release properties of SVs at hair-cell ribbon synapses. |
url |
http://europepmc.org/articles/PMC2673039?pdf=render |
work_keys_str_mv |
AT josefgtrapani synaptojanin1isrequiredfortemporalfidelityofsynaptictransmissioninhaircells AT nikolausobholzer synaptojanin1isrequiredfortemporalfidelityofsynaptictransmissioninhaircells AT weikemo synaptojanin1isrequiredfortemporalfidelityofsynaptictransmissioninhaircells AT susanebrockerhoff synaptojanin1isrequiredfortemporalfidelityofsynaptictransmissioninhaircells AT teresanicolson synaptojanin1isrequiredfortemporalfidelityofsynaptictransmissioninhaircells |
_version_ |
1726006505145106432 |