Angelika Doetzlhofer PhD

Associate Professor of Neuroscience
Telephone Number: 410-614-9215
Fax Number: 410-614-8033

The Solomon H. Snyder Department of Neuroscience
Johns Hopkins University
School of Medicine
855 North Wolfe St.
Baltimore, MD 21205
Room: Rangos 433
Areas of Research
Developmental Neuroscience
Cellular + Molecular Neuroscience
Neurobiology of Disease

Graduate Program Affiliations

Neuroscience Training Program

Biochemistry, Cellular and Molecular Biology Graduate Program

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    Shown is the surface of the murine auditory sensory epithelium at birth. Hair cells are patterned into one row of inner hair cells (red) and three rows of outer hair cells (red). The inner and outer hair cell regions are separated by specialized supporting cells –so called inner and outer pillar cells (green). P75 (green) marks the apical surface of pillar cells and actin-rich hair cell stereocilia are visualized using phalloidin staining (red). (See Doetzlhofer et al., Dev Cell. 2009 Jan;16(1):58-69.)

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    Shown are in vitro generated hair cells. The Math1/GFP+ hair cells (green nucleus) posses stereocilia-like projections stained with phalloidin (blue) and express mature hair cell markers such as myosinVIIa (red). (Cover image, Doetzlhofer et al., Dev Biol. 2004 Aug 15;272(2):432-47).

Cell specification and differentiation in the mammalian auditory system

Auditory hair cells, located in the inner ear cochlea are critical for our ability to detect sound.

In mammals, neural innervated hair cells come in two flavors: inner hair cells, which are our primary mechanoreceptor and relay sound information to the brain and the signal amplifying outer hair cells. Inner and outer hair cells are structurally and functionally supported by different types of glial-like supporting cells with which they share a close lineage relationship. Despite their importance for our ability to hear, little is known about how the different hair cell and supporting cell lineages are specified and what molecular cues trigger their differentiation. A main goal of my laboratory is to identify and characterize the molecular mechanisms underlying hair cell and supporting cell specification and differentiation in the mammalian auditory system.                                                

An associated interest is to identify the molecular roadblocks preventing mammalian hair cell regeneration. In mammals, hair cell generation is limited to embryonic development. Lost hair cells are not replaced leading to deafness and balance disorders. However, in non-mammalian vertebrates, supporting cells undergo a process of de-differentiation after hair cell loss, and are able to replace lost hair cells by either cell division or direct trans-differentiation. We recently showed that purified mammalian supporting cells retain some hair cell progenitor-like qualities and are able to trans-differentiate into hair cell in vitro. These results suggest that the lack of mammalian hair cell regeneration is likely due to an absence or blockage of regenerative signals.

Currently projects in the laboratory address: 1) Function of the Notch signaling pathway in supporting cell differentiation and hair cell regeneration; 2) Function of Lin28b/ Let-7 pathway in cochlear development; 3) Identification and functional characterization of nuclear factors that control specification of hair cell and supporting cell subtypes.  Our investigations make use of mouse genetic approaches, including inner ear-specific conditional gene targeting and in vitro manipulations of gene function in cochlea tissue and primary cell culture systems.

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