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...

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Main Authors: Josef G Trapani, Nikolaus Obholzer, Weike Mo, Susan E Brockerhoff, Teresa Nicolson
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
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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
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