Ca2+ Dynamics of Gap Junction Coupled and Uncoupled Deiters’ Cells in the Organ of Corti in Hearing BALB/c Mice

Author:

Moysan Louise1ORCID,Fazekas Fruzsina1,Fekete Adam2,Köles László34,Zelles Tibor345ORCID,Berekméri Eszter14

Affiliation:

1. Department of Zoology, University of Veterinary Medicine Budapest, H-1078 Budapest, Hungary

2. Program in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada

3. Department of Oral Biology, Semmelweis University, H-1089 Budapest, Hungary

4. Department of Pharmacology and Pharmacotherapy, Semmelweis University, H-1089 Budapest, Hungary

5. Laboratory of Molecular Pharmacology, Institute of Experimental Medicine, H-1083 Budapest, Hungary

Abstract

ATP, as a paracrine signalling molecule, induces intracellular Ca2+ elevation via the activation of purinergic receptors on the surface of glia-like cochlear supporting cells. These cells, including the Deiters’ cells (DCs), are also coupled by gap junctions that allow the propagation of intercellular Ca2+ waves via diffusion of Ca2+ mobilising second messenger IP3 between neighbouring cells. We have compared the ATP-evoked Ca2+ transients and the effect of two different gap junction (GJ) blockers (octanol and carbenoxolone, CBX) on the Ca2+ transients in DCs located in the apical and middle turns of the hemicochlea preparation of BALB/c mice (P14–19). Octanol had no effect on Ca2+ signalling, while CBX inhibited the ATP response, more prominently in the middle turn. Based on astrocyte models and using our experimental results, we successfully simulated the Ca2+ dynamics in DCs in different cochlear regions. The mathematical model reliably described the Ca2+ transients in the DCs and suggested that the tonotopical differences could originate from differences in purinoceptor and Ca2+ pump expressions and in IP3–Ca2+ release mechanisms. The cochlear turn-dependent effect of CBX might be the result of the differing connexin isoform composition of GJs along the tonotopic axis. The contribution of IP3-mediated Ca2+ signalling inhibition by CBX cannot be excluded.

Funder

research fund of the National Research, Development and Innovation Office of Hungary

Ministry of Innovation and Technology of Hungary from the National Research, Development and Innovation Fund

University of Veterinary Medicine Budapest’s support of Young Researchers 2023

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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