Keratinization involves the expression of numerous differentiated traits. Variations in the pattern of keratinization in oral mucosa and epidermis reflect varying degrees of expression of these traits. To determine how keratinization is controlled, several markers of epithelial differentiation will be examined in cultured human keratinocytes. I. Keratin Production: Kinetic studies of keratin synthesis in cultured cells suggest that keratin production is controlled differently in the lower and upper strata of keratinizing epithelia. To test this hypothesis, aspects of keratin synthesis will be characterized in keratinocytes stimulated to undergo enhanced keratinization in culture. Keratin is heavily phosphorylated. Experiments will define the kinetics of this reaction during maturation, and the role of these charged groups in filament assembly. II. Terminal Differentiatio (TD): An assay developed to measure the rate of TD will be used to explore two central questions in keratinization...does TD follow or precede transit out of the basal layer? and, is the probability of TD following cell replication a fixed property of the keratinocyte. III. Productive Viral Replication: Replication of Adenovirus type 2 (Ad-2) is a newly discovered marker of keratinocyte differentiation. To determine how viral replication is blocked in infected basal cells, the transcriptional activity and physical state of Ad-2 DNA will be examined in these cells. Human papilloma virus (HPV) has been shown to persist in keratinocytes as stable episome and to synthesize viral antigens after repeated passage of infected cells. To explore this model of viral latency, HPV RNA will be isolated from early and late passage cells. Transcripts will be mapped and where possible used to identify viral specific proteins. IV. Somatic Cell Genetics of Keratinocytes: To elucidate the genetic controls in keratinization, expression of keratinocyte markers will be studied in human keratinocyte X mouse fibroblast hybrids. Where possible, chromosomal mapping will be performed. These experiments draw upon disciplines and techniques not traditionally used in the study of keratinization. It is hoped that concepts and mechanisms heretofore unknown, will be discovered and that a useful body of knowledge will be generated concerning disorders of keratinization.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE004511-10
Application #
3219085
Study Section
Oral Biology and Medicine Study Section (OBM)
Project Start
1979-05-01
Project End
1986-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
10
Fiscal Year
1985
Total Cost
Indirect Cost
Name
State University New York Stony Brook
Department
Type
Schools of Dentistry/Oral Hygn
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
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Ghazizadeh, Soosan; Katz, Anne B; Harrington, Robin et al. (2004) Lentivirus-mediated gene transfer to human epidermis. J Investig Dermatol Symp Proc 9:269-75
Ghazizadeh, Soosan; Kalish, Richard S; Taichman, Lorne B (2003) Immune-mediated loss of transgene expression in skin: implications for cutaneous gene therapy. Mol Ther 7:296-303
Ghazizadeh, S; Doumeng, C; Taichman, L B (2002) Durable and stratum-specific gene expression in epidermis. Gene Ther 9:1278-85
Albers, K M; Greif, F; Setzer, R W et al. (1987) Cell-cycle withdrawal in cultured keratinocytes. Differentiation 34:236-40