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Koleilat, A.

Publications and source records attributed to Koleilat, A..

2 recordsLinked to original sources

Three-dimensional structure of inner ear hair cell mitochondrial networks and ribbon synapses in a zebrafish model of Usher syndrome type 1B

Inner ear hair cells are the fundamental unit of sound and vibration detection in inner ear and lateral line structures. Our understanding of the structure and ultrastructure of hair cells has heretofore relied upon two-dimensional imaging. The development of serial block-face scanning electron microscopy (SBFSEM) changes this paradigm and allows for ultrastructural evaluation of hair cells in three-dimensions. This is the first report of SBFSEM analysis in the myo7aa-/- mutant where we evaluated several attributes of zebrafish hair cells from the inner ear cristae in both wildtype and myo7aa-/- mutant zebrafish through three-dimensional reconstruction. We describe ribbon synapse number, location, and volume, mitochondrial localization, and innervation for individual hair cells. We determined that myo7aa-/- mutant ribbon synapses have a smaller volume and surface area; however, all other hair cell attributes investigated were not significantly different between the mutant and wildtype zebrafish. These findings are critical for the development of therapies for deafness caused by mutations in myo7aa, as this study supports that the necessary hair cell machinery for hearing is largely intact. In addition, the methodology and measurements developed in this study provide a guide for the evaluation of zebrafish hair cells using SBFSEM.

cell biology↗

L-type voltage-gated calcium channel agonists improve hearing loss and modify ribbon synapse morphology in the zebrafish model of Usher Syndrome Type 1

Usher Syndrome (USH) is the most common cause of human deaf/blindness. The zebrafish myo7aa-/- mutant, faithfully models USH1; homozygous zebrafish are deaf and exhibit circular swimming. We hypothesized that hair cell morphology would differ in myo7aa-/- mutants compared to wild type. We also tested the hypothesis that agonists of L-type voltage-gated calcium channels would alter ribbon synapse morphology and behavior of zebrafish myo7aa-/- mutants. We discovered that myo7aa-/- zebrafish have fewer glutamatergic vesicles tethered to hair cell ribbon synapses, yet maintain a comparable ribbon area. We identified that myo7aa-/- mutants have fewer total active hair cells, fewer total CTBP2 expressing puncta, and an altered distribution of CTBP2 puncta compared to wildtype. We also identified that myo7aa-/- mutants have fewer active post-synaptic cells and fewer total MAGUK puncta, compared to wildtype. Behaviorally, myo7aa-/- mutant fish have abnormal swimming as measured by larger absolute smooth orientations and have little to no acoustic startle. Treatment with L-type voltage-gated calcium channel agonists altered the abnormal cell and behavioral phenotypes toward wildtype. Our data supports that L-type voltage-gated calcium channel agonists induce morphological changes at the ribbon synapse--in both the number of tethered vesicles and the distribution of CTBP2 puncta, shifts swimming behavior towards wildtype swimming and improves acoustic startle response. Summary StatementWe identified that the hair cell biology and behavior of the myo7aa-/- mutant differs from wildtype and this difference can be rescued using L-type voltage-gated calcium channel agonists.

neuroscience↗