The goal of our research is to understand the timing and molecular mechanisms that control patterning and cell fate specification in the developing inner ear. The inner ear, unique to vertebrates, houses the peripheral receptors for the sensations of hearing and balance. It is composed of a complex three-dimensional arrangement of constituent cells which includes neurons, receptors grouped into distinct sensory organs, and non-sensory tissues that form the ducts, tubules and specialized secretory epithelia needed for proper homeostasis of the fluid components. In humans and animal models, disruption of the precise morphology of the inner ear due to congenital defects or disease can result in deafness and/or to difficulties with balance and equilibrium. Our efforts to understand the fundamental defects that result in inner ear abnormalities are focused on both the normal processes of development and on the cascade of events that can arise as a result of specific genetic defects. In this study, we focus on Wnt signaling. This family of signaling molecules has been highly conserved during evolution, and is linked to many aspects of development including control of cell proliferation, cell fate specification, morphogenetic movements, axon guidance and orientation of cells along the body axis. We have completed a comprehensive mapping of the spatial and temporal expression patterns of 28 Wnt-related genes during development of the avian inner ear. Our survey included ligands, receptors and secreted inhibitors. The data have led to several hypotheses about the role of Wnts in different aspects of ear development.
The Specific Aims are (1) to explore the function of Wnt/2-catenin signaling as a switch between auditory and vestibular (macular) sensory organ fates in the cochlear duct;(2) to explore the function of Wnt signaling as a repulsive axon guidance cue in the developing inner ear;and (3) to explore the function of radial gradients of Wnt-related molecules across the auditory sensory epithelium. Our findings may provide baseline data for therapeutic strategies to direct stem cells along different developmental fates for repair or replacement of damaged inner ear cells. Our research program uses the chicken embryo to study the molecular pathways underlying development of the inner ear. The long-term goal of our research is to determine whether the molecules we identify may be linked to genetic causes of congenital deafness in humans, with the hope that this knowledge might be applied to therapeutic treatments aimed at the regeneration or repair of inner ear cells.
Our research program uses the chicken embryo to study the molecular pathways underlying development of the inner ear. The long-term goal of our research is to determine whether the molecules we identify may be linked to genetic causes of congenital deafness in humans, with the hope that this knowledge might be applied to therapeutic treatments aimed at the regeneration or repair of inner ear cells.
|Battisti, Andrea C; Fantetti, Kristen N; Moyers, Bryan A et al. (2014) A subset of chicken statoacoustic ganglion neurites are repelled by Slit1 and Slit2. Hear Res 310:1-12|
|Jiang, Han; Wang, Lingyan; Beier, Kevin T et al. (2013) Lineage analysis of the late otocyst stage mouse inner ear by transuterine microinjection of a retroviral vector encoding alkaline phosphatase and an oligonucleotide library. PLoS One 8:e69314|
|Munnamalai, Vidhya; Fekete, Donna M (2013) Wnt signaling during cochlear development. Semin Cell Dev Biol 24:480-9|
|Stoller, Michelle L; Chang, Henry C; Fekete, Donna M (2013) Bicistronic gene transfer tools for delivery of miRNAs and protein coding sequences. Int J Mol Sci 14:18239-55|
|Fantetti, Kristen N; Fekete, Donna M (2011) Dissection and culture of chick statoacoustic ganglion and spinal cord explants in collagen gels for neurite outgrowth assays. J Vis Exp :|
|Liang, Hongzi; Fekete, Donna M; Andrisani, Ourania M (2011) CtBP2 downregulation during neural crest specification induces expression of Mitf and REST, resulting in melanocyte differentiation and sympathoadrenal lineage suppression. Mol Cell Biol 31:955-70|
|Sienknecht, Ulrike J; Anderson, Brittany K; Parodi, Rebecca M et al. (2011) Non-cell-autonomous planar cell polarity propagation in the auditory sensory epithelium of vertebrates. Dev Biol 352:27-39|
|Kilpatrick, L A; Li, Q; Yang, J et al. (2011) Adeno-associated virus-mediated gene delivery into the scala media of the normal and deafened adult mouse ear. Gene Ther 18:569-78|
|Fantetti, Kristen N; Zou, Yimin; Fekete, Donna M (2011) Wnts and Wnt inhibitors do not influence axon outgrowth from chicken statoacoustic ganglion neurons. Hear Res 278:86-95|
|Li, Haiqiong; Fekete, Donna M (2010) MicroRNAs in hair cell development and deafness. Curr Opin Otolaryngol Head Neck Surg 18:459-65|
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