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David R. Hinton

Professor

Pathology, Neurosurgery, Ophthamology
Keck School of Medicine

Send E-mail to:   dhinton@usc.edu 
Telephone: 323-442-6617Fax: 323-442-6688
Office: DOH 213Mail Code: 9092 HSC

Education:
MD 1978 Medicine - University of Toronto, Ontario, Canada
FRCP(C) 1983 Neuropathology - University of Toronto, Ontario, Canada

Postdoctoral Research Fellowship:
1978 - 1979 University of Toronto, Ontario, Canada

Started at USC: 1988

Research Topics: Aging, Gene Therapy, Vision Research, Cellular Neurobiology

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Research Description

Dr. Hinton's research focuses on the response of the outer retina to injury and how this response can lead to blinding disorders such as proliferative vitreoretinopathy (PVR) and choroidal neovascularization (CNV). PVR occurs as a wound healing response to severe ocular trauma or retinal detachment while CNV occurs primarily as a blinding complication of age-related macular degeneration. He has established the central role of the retinal pigment epithelial (RPE) cell in these disorders and has demonstrated novel mechanisms for growth factor activation of these cells. He is investigating the pathologic consequences of this activation on RPE migration, proliferation and gene expression. In particular he is interested in how the activated RPE cell can alter the local retinal microenvironment to promote the development of intraocular proliferative membranes and neovascularization from the adjacent choroidal endothelium. Dr. Hinton has developed and validated several in vitro and in vivo models of PVR and CNV and has used these models to elucidate basic mechanisms of disease and to evaluate novel therapeutic approaches to the disorders. He is especially interested in therapeutic approaches involving manipulation of growth factor receptors, and their intracellular signaling pathways. Dr. Hinton is also interested in the pathophysiology of viral infection in the brain and its relationship to demyelination. He is particularly interested in the mechanisms involved in leukocyte infiltration into the brain in viral infection.



10 Selected Publications:
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Ireland DD,Stohlman SA,Hinton DR,Kapil P,Silverman RH,Atkinson RA,Bergmann CC - RNase L mediated protection from virus induced demyelination. - PLoS Pathog [2009] Oct;5(10):e1000602 PubMed

Zhu D,Sreekumar PG,Hinton DR,Kannan R - Expression and regulation of enzymes in the ceramide metabolic pathway in human retinal pigment epithelial cells and their relevance to retinal degeneration. - Vision Res [2009] Sep 16;(): PubMed

Tran ND,Kim S,Vincent HK,Rodriguez A,Hinton DR,Bullock MR,Young HF - Aquaporin-1-mediated cerebral edema following traumatic brain injury: effects of acidosis and corticosteroid administration. - J Neurosurg [2009] Sep 4;(): PubMed

He S,Kumar SR,Zhou P,Krasnoperov V,Ryan SJ,Gill PS,Hinton DR - Soluble EphB4 inhibits PDGF-induced RPE migration in vitro. - Invest Ophthalmol Vis Sci [2009] Aug 20;(): PubMed

Chothe P,Thakkar SV,Gnana-Prakasam JP,Ananth S,Hinton DR,Kannan R,Smith SB,Martin PM,Ganapathy V - Identification of a Novel Sodium-coupled Oligopeptide Transporter (SOPT2) in Mouse and Human Retinal Pigment Epithelial Cells. - Invest Ophthalmol Vis Sci [2009] Jul 30;(): PubMed

Sadler TR,Khodavirdi AC,Hinton DR,Holschneider DP - Snap-frozen brain tissue sections stored with desiccant at ambient laboratory conditions without chemical fixation are resistant to degradation for a minimum of 6 months. - Appl Immunohistochem Mol Morphol [2009] Mar;17(2):165-71 PubMed

Sonoda S,Spee C,Barron E,Ryan SJ,Kannan R,Hinton DR - A protocol for the culture and differentiation of highly polarized human retinal pigment epithelial cells. - Nat Protoc [2009] ;4(5):662-73 PubMed

Sreekumar PG,Kannan R,Hinton DR - There are three major families of crystallins: misnaming of alphaB crystallin. - Acta Physiol (Oxf) [2009] Apr;195(4):503; author reply 503 PubMed

Kim YH,He S,Kase S,Kitamura M,Ryan SJ,Hinton DR - Regulated secretion of complement factor H by RPE and its role in RPE migration. - Graefes Arch Clin Exp Ophthalmol [2009] Feb 13;(): PubMed

Zhu D,Wu J,Spee C,Ryan SJ,Hinton DR - BMP4 mediates oxidative stress-induced retinal pigment epithelial cell senescence and is over expressed in age-related macular degeneration. - J Biol Chem [2009] Jan 21;(): PubMed


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