Research in the laboratory is focused on basic developmental mechanisms guiding cellular polarization, morphogenesis, and axon guidance within the cochlea and vestibular maculae.
We anticipate that healing the damaged ear will include a reiteration of those developmental events that first built it. Therefore, understanding those processes is an important prerequisite for the success of hearing and balance therapies.
Ongoing Research
Vestibular Hair Cell Development and the Formation of Planar Bipolarity (NIH/NIDCD R01DC013066)
In the vestibular system of the inner ear, motion is detected via the mechanical deflection of a bundle of stereocilia located at the top of sensory receptor hair cells. The bundle is anatomically and functionally polarized because only deflections towards a lone kinocilium positioned at one side of the hair cell surface produce excitatory responses to acceleration or gravity. Thus, the range of motion that can be detected by any individual hair cell is determined by the polarized orientation of its stereociliary bundle.
In order to generate a complete sensory representation of motion in space, vestibular hair cells of the utricle and saccule are found in arrays spanning the full 360° range of bundle orientations. This is achieved in part through Planar Bipolarity. Thus, while the stereociliary bundles of neighboring hair cells are similarly oriented, the hair cells are also divided between two groups with oppositely oriented bundles that respond to motion in opposite directions. These groups are separated by a single intercellular junction often referred to as the Line of Polarity Reversal (LPR).
Our goal is to identify the cellular and molecular mechanisms that direct the development of Planar Bipolarity through formation of the LPR, and thereby establish this sensory representation of gravity and acceleration. We are pursuing this using a combination of knockout and transgenic mouse models.
PCP Signaling during Axon Guidance and Cochlear Innervation (NIH/NIDCD 1R01DC018040)
The cochlea is innervated by spiral ganglion neurons, which relay sound information from sensory receptor hair cells to central auditory targets. A common pathology in deafness models is the loss of synapses between the hair cells and their spiral ganglion neurons. Thus, any successful hearing restoration therapy will include reinnervation of the damaged cochlea, a process which is likely to mimic the innervation that occurs during development. As a result, understanding early developmental events is an important and essential prerequisite for many therapeutic strategies.
A subset of spiral ganglion neurons has nociceptive characteristics and are thus equipped to detect acoustic trauma, which may be important for preserving function. These are the type II spiral ganglion neurons, which constitute a minority of cochlear afferents but innervate all three rows of outer hair cells. The development of type II neurons is unique because their peripheral axons project beyond the inner hair cells and subsequently make a distinct 90° turn towards the cochlear base to synapse with multiple outer hair cells. While many aspects of outer hair cell innervation are unknown, we have found that planar cell polarity (PCP) signaling is required for the 90° turn that directs the peripheral axon towards the cochlear base.
The goal of this research is to understand how a cell polarity signaling pathway influences growth cone behavior. We have found that the PCP proteins are not required in the growth cone itself but rather in the environment that the growth cone is navigating. An exciting possibility is that PCP signals emanating from organ of Corti supporting cells provides guidance cues. This hypothesis is being directly tested using a combination of knockout and transgenic mouse models.