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Dr. David Molea
Postdoctoral Fellow


Cochlear implants and the possibility of restoring hearing by regenerating the sensory receptors in the human ear, depend upon the presence and survival of statoacoustic ganglion (SAG) neurons to connect them to the brain. An understanding of the differentiation of these two cell types is needed to guide the regeneration of whichever cell type is needed to restore hearing.

Dr. Molea’s main project examines the role of the zinc-finger transcription factors Zic1 and Zic2 in the development of SAG neurons, hair cells, and supporting cells types in the inner ear. Zic1 and Zic2, which are involved in early neurogenesis and the differentiation of specific neuronal cell types in the central and peripheral nervous systems, are also expressed in the otocyst during the time period when SAG neuronal precursors and the sensory epithelia differentiate. Since the Zic genes are regulated by the BMP signaling pathway, this work is a prerequisite for further studies testing the roles of the BMP4 and BMP antagonist during inner ear development.


Dr. Molea, in collaboration with Dr. Lynne Bianchi (Oberlin College), is also trying to isolate otocyst derived factors responsible for SAG neuron survival and neurite outgrowth using protein purification and proteomics approaches.

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