Sonic Hedgehog Signaling in Inner Ear Organoid Development

dc.contributor.advisorHashino, Eri
dc.contributor.authorLongworth-Mills, Emma
dc.contributor.otherJones, Kathryn
dc.contributor.otherRobling, Alexander
dc.contributor.otherZimmers, Teresa
dc.contributor.otherChen, Jinhui
dc.date.accessioned2019-08-29T12:43:48Z
dc.date.available2021-08-21T09:30:10Z
dc.date.issued2019-08
dc.degree.date2019en_US
dc.degree.disciplineDepartment of Anatomy & Cell Biology
dc.degree.grantorIndiana Universityen_US
dc.degree.levelPh.D.en_US
dc.descriptionIndiana University-Purdue University Indianapolis (IUPUI)en_US
dc.description.abstractLoss of the finite cochlear hair cells of the inner ear results in sensorineural deafness. Human cochlear hair cells do not regenerate, and there is no cure for deafness. Our laboratory has established a three-dimensional culture system for deriving functional sensory hair cells from human pluripotent stem cells. A major limitation of this approach is that derived hair cells exhibit a morphological and gene expression phenotype reflective of native vestibular hair cells. Previous studies have shown that establishment of localized domains of gene expression along the dorso-ventral axis of the developing otic vesicle is necessary for proper morphogenesis of both auditory and vestibular inner ear structures. Sonic hedgehog (SHH) signaling has been shown to play a key role in specification of the ventral otic vesicle and subsequent cochlear development. Here, SHH treatment was pursued as a potential strategy for inducing a patterning phenotype permissive to cochlear induction in vitro. Single-cell RNAsequencing analysis revealed that while treatment with the SHH pathway agonist Purmorphamine reduced expression of markers for the vestibular-yielding dorsal otic vesicle, upregulation of ventral otic marker genes was modest. More strikingly, the number of otic progenitors exhibiting a neuroprogenitor phenotype increased in response to Purmorphamine treatment. These results suggest that SHH pathway modulation in early-stage inner ear organoids may bias their differentiation toward a neural lineage at the expense of an epithelial lineage. The present study is the first to evaluate the patterning phenotype of human stem cell derived otic progenitors, and sheds light on the transcriptomic profile at this critical point of inner ear development. This study may also cultivate future efforts to derive cochlear cell types as well as inner ear neural cell types from human pluripotent stem cells, and contribute to the establishment of a more complete in vitro model of inner ear development.en_US
dc.description.embargo2021-08-21
dc.identifier.urihttps://hdl.handle.net/1805/20693
dc.identifier.urihttp://dx.doi.org/10.7912/C2/2120
dc.language.isoen_USen_US
dc.subjectInner earen_US
dc.subjectOrganoiden_US
dc.subjectOticen_US
dc.subjectPatterningen_US
dc.subjectSonic hedgehogen_US
dc.subjectStem cellen_US
dc.titleSonic Hedgehog Signaling in Inner Ear Organoid Developmenten_US
dc.typeDissertation
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