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Publication : Intrinsic planar polarity mechanisms influence the position-dependent regulation of synapse properties in inner hair cells.

First Author  Jean P Year  2019
Journal  Proc Natl Acad Sci U S A Volume  116
Issue  18 Pages  9084-9093
PubMed ID  30975754 Mgi Jnum  J:274644
Mgi Id  MGI:6297130 Doi  10.1073/pnas.1818358116
Citation  Jean P, et al. (2019) Intrinsic planar polarity mechanisms influence the position-dependent regulation of synapse properties in inner hair cells. Proc Natl Acad Sci U S A 116(18):9084-9093
abstractText  Encoding the wide range of audible sounds in the mammalian cochlea is collectively achieved by functionally diverse type I spiral ganglion neurons (SGNs) at each tonotopic position. The firing of each SGN is thought to be driven by an individual active zone (AZ) of a given inner hair cell (IHC). These AZs present distinct properties according to their position within the IHC, to some extent forming a gradient between the modiolar and the pillar IHC side. In this study, we investigated whether signaling involved in planar polarity at the apical surface can influence position-dependent AZ properties at the IHC base. Specifically, we tested the role of Galphai proteins and their binding partner LGN/Gpsm2 implicated in cytoskeleton polarization and hair cell (HC) orientation along the epithelial plane. Using high and superresolution immunofluorescence microscopy as well as patch-clamp combined with confocal Ca(2+) imaging we analyzed IHCs in which Galphai signaling was blocked by Cre-induced expression of the pertussis toxin catalytic subunit (PTXa). PTXa-expressing IHCs exhibited larger CaV1.3 Ca(2+)-channel clusters and consequently greater Ca(2+) influx at the whole-cell and single-synapse levels, which also showed a hyperpolarized shift of activation. Moreover, PTXa expression collapsed the modiolar-pillar gradients of ribbon size and maximal synaptic Ca(2+) influx. Finally, genetic deletion of Galphai3 and LGN/Gpsm2 also disrupted the modiolar-pillar gradient of ribbon size. We propose a role for Galphai proteins and LGN in regulating the position-dependent AZ properties in IHCs and suggest that this signaling pathway contributes to setting up the diverse firing properties of SGNs.
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