dr dan jagger
Research
Themes
- Dr
- Dan
- James
- Jagger
- Dr Dan Jagger
- Tel: 020 7679 8930
- Ex: 28930
- Fax: 020 7679 8990
- d.jagger@ucl.ac.uk
- Website
- https://iris.ucl.ac.uk/images/profile/DJAGG65.jpg
- 2002-10-01
- 1016
- UCL Ear Institute
- 332 Gray's Inn Rd
- London
- WC1X 8EE
- RESSRF
- 2003-10-01
- 1
- Senior Lecturer
- HP
- The Ear Institute
- FBRS
- Faculty of Brain Sciences
- 2002-10-01
Research Summary
I’m interested in the proteins that make cochlear cells work, particularly those in supporting cells that look after cochlear hair cells and neurons. Hair cells can’t regenerate; if you damage them they’re gone
forever. They have to be kept in great condition for a lifetime. The supporting cells remove any nasty substances from the environment around hair cells to keep them happy. By understanding how supporting cells do their job, we can begin to develop therapies that could help all of us to keep our hair cells for longer.
In other research, I have a growing interest in the hearing impairment observed in certain “ciliopathies”, such as Alström syndrome. It is not currently obvious how mutations in proteins involved in the function of the cilium can cause loss of hair cells.
Areas currently under investigation:
- The characteristics of gap junctions in the inner ear
- The effects of connexin mutations on cochlear physiology
- The development of afferent neurons in the cochlea
- The contribution of cilia proteins to cochlear development
- 1291
- Role of gap junctions and regulatory proteins in the long-term maintenance of hearing.
- 524
- Sensory cell death in the inner ear, repair of the sensory epithelia and protection and regeneration of hair cells
Assessing PCP in the cochlea of mammalian ciliopathy models.
Contractility in Type III Cochlear Fibrocytes Is Dependent on Non-muscle Myosin II and Intercellular Gap Junctional Coupling.
Development of gap junctional intercellular communication within the lateral wall of the rat cochlea.
Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity.
The Membrane Properties of Cochlear Root Cells are Consistent with Roles in Potassium Recirculation and Spatial Buffering.
Cochlear supporting cells
Patterns of expression of Bardet-Biedl syndrome proteins in the mammalian cochlea suggest noncentrosomal functions
Connexins in the Inner Ear
Academic Background
-
Award YearQualificationInstitution
-
1996PhDUniversity of Bristol
-
1993BSc HonsUniversity of Newcastle upon Tyne
Biography
I am primarily a physiologist, and my main interest is in the homeostasis of sensory “hair cells” in the cochlea.
I collaborate with a number of people across UCL and in other UK institutions.
At the Ear Institute I work closely with Andy Forge and Barbara Cadge.
In my lab at the moment are Regina Nickel (post-doc) and John Kelly (DRUK-funded PhD student).
- Auditory
- Auditory system disorders
- Cochlea
- Cochlear homeostasis
- Confocal microscopy
- Deafness
- Electrophysiological recording techniques
- Electrophysiology
- Fluorescence microscopy techniques
- Hearing and balance
- Immunohistochemistry
- Ion channels
- Light microscopic techniques
- Neurophysiology
- Neuroscience
- Patch-clamp recording
- Protein transport/localisation
- Sensory transduction
- Single-channel recording
- Synapse
- Time-lapse imaging
- JEGAL30
- dr jonathan gale
- DLBEC91
- prof david becker
- PLBEA59
- prof philip beales
- AFORG20
- prof andrew forge
Page last modified on 01 dec 11 09:39
