prof andrew forge
Research
Themes
Contacts
- Prof
- Andrew
- Forge
- Prof Andrew Forge
- Tel: 020 7679 8983
- Ex: 28983
- Fax: 020 7679 8990
- a.forge@ucl.ac.uk
- Website
- https://iris.ucl.ac.uk/images/profile/AFORG20.jpg
- 1987-08-01
Address
- 855
- UCL Ear Institute
- 332 Gray's Inn Rd
- London
- WC1X 8EE
Appointment
- ACAPRO
- 1987-08-01
- 1
- Professor of Auditory Cell Biology
- HP
- The Ear Institute
- FBRS
- Faculty of Brain Sciences
Joined UCL
- 1987-08-01
Research Summary
The loss of the sensory hair cells from the cochlea (the hearing organ) is the major cause of deafness. Loss of the hair cells from vestibular system is a major contributor to balance dysfunction and the predominant underlying cause of falls in the elderly. The work in the laboratory aims at:Understanding how hair cells die and the reasons for the progressive increase in hair cell loss once initiated, and identifying possible for pharmaceutical interventions to protect hair cells from lethal damage and/or prevent the progression of hair cell loss once initiated.
Characterising the process of repair of the cochlear and vestibular sensory epithelia when hair cells die; the cytoskeletal re-arrangements through which the non-sensory supporting cells that surround each hair cell close the lesions; and the subsequent molecular and cellular nature of the re-organisation of the sensory epithlelia that occurs following hair cell loss
Regeneration of hair cells and possible cell replacement strategies, including the use of progenitor cells derived from inner tissues and of stem cells
The maintenance of the inner ears environment that enables the proper functioning of hair cells and how that environment changes when hair cells die so that the likely ability of replacement hair cells to function properly can be assessed. A major part of this work involves investigations of intercellular communication via gap junctions, and the role of gap junctions and connexins in repair and recovery processes in the inner ear.
The work involves the use of whole animal models and organotypic cultures. Techniques have been developed for the maintenance of inner ear tissues of mammals, chickens and newts in culture. Hair cell regeneration occurs spontaneously in the inner ears of non-mammalian vertebrates; the examination of chicks and newts provides enables comparisons with the mammalian inner ear. We have also been able to maintain the vestibular sensory epithelia from humans in organotypic culture. The human tissue can be obtained from patients undergoing operations for acoustic neuromas and this presents the only opportunity to examine human inner ear tissues under experimental conditions. We are in the process of establishing a national consortium of surgeons who operate on such patients in order to obtain human vestibular material for our studies.
Research Activities
- 680
- Actin dynamics in cell motility and tissue mechani
- 1444
- Deafness genetics
- 1382
- Low-frequency hearing
- 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
1 - 10 of 142 Publications
Contractility in Type III Cochlear Fibrocytes Is Dependent on Non-muscle Myosin II and Intercellular Gap Junctional Coupling.
Journal article
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β3-integrin is required for differentiation in OC-2 cells derived from mammalian embryonic inner ear.
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Assessing PCP in the cochlea of mammalian ciliopathy models.
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Hearing in 44-45 year olds with m.1555A>G, a genetic mutation predisposing to aminoglycoside-induced deafness: a population based cohort study.
Journal article
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Hair bundle defects and loss of function in the vestibular end organs of mice lacking the receptor-like inositol lipid phosphatase PTPRQ.
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Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity.
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Development of gap junctional intercellular communication within the lateral wall of the rat cochlea.
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The aneurogenic limb identifies developmental cell interactions underlying vertebrate limb regeneration.
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A congenital activating mutant of WASp causes altered plasma membrane topography and adhesion under flow in lymphocytes.
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Additional Information
- Auditory
- Autophagy
- Balance dysfunction
- Cell culture
- Cell tracking
- Cochlea
- Confocal microscopy
- Connectivity
- Deafness
- Development
- Differentiation
- Electron Microscopy
- Electrophysiological recording techniques
- Fluorescence microscopy techniques
- Hearing and balance
- Immunohistochemistry
- Light microscopic techniques
- Regeneration
- Repair
- Sensory transduction
- Survival, protection and regeneration of hair cells
- Transgenic mice
Collaborators
- JEGAL30
- dr jonathan gale
- DLBEC91
- prof david becker
- AJHAR52
- prof alison hardcastle
- BBACK51
- dr bradford backus
- TMARQ91
- mr torsten marquardt
- DJAGG65
- dr dan jagger
- DTKEM02
- prof david kemp
- PLBEA59
- prof philip beales
- SSAEE03
- prof shakeel saeed
- PTKHA24
- prof peng khaw
- SJDAW90
- dr sally dawson
- MBAIL59
- dr maryse bailly
External Collaborators
- 607
- Dr Carlos Juardo Orellana
Page last modified on 31 oct 11 10:41
