Abstract
ABSTRACTThe relationship between Ca2+action potential (AP) activity in immature inner hair cells (IHCs) and the spontaneous ATP-dependent intercellular Ca2+signaling in cochlear non-sensory cells (NSCs) of the greater epithelial ridge (GER) is unclear. Here, we determined that IHCs fired asynchronous Ca2+APs also in the absence of Ca2+activity in the GER. Patch clamp recordings from IHCs isolated from the rest of the sensory epithelium confirmed that this firing activity is an intrinsic property of immature IHCs. However, frequency, correlation index and burst duration of IHC APs increased significantly during Ca2+wave propagation in NSCs, and depended on wave extension in the GER. Furthermore, IHC depolarization under whole cell patch clamp conditions triggered Ca2+signals in nearby NSCs with a delay that was proportional to the distance from the stimulated IHC. Thus the immature mammalian cochlea supports bidirectional exchange of Ca2+signals between IHCs and NSCs.IMPACT STATEMENTIn inner hair cells of the developing mammalian cochlea, Ca2+action potentials are both intrinsic and bidirectionally coupled to the ATP-dependent Ca2+signaling of the surrounding non-sensory cells.
Publisher
Cold Spring Harbor Laboratory