During the next five years, we will continue to study epidermis and epidermal appendages in health and disease by focusing on keratin gene expression in a number of model systems. During this period, we shall use guinea pig epidermis, mouse hair root cells, cell lines such as ME 180 derived from pathologic human tissue and human epidermal biopsies to identify and characterize the keratin genes and to prepare radiolabelled probes of the study of gene expression. Probes will be used to analyze a number of physiologic states, such as mitosis and againg, a number of pathologic conditions, such as tumors, psoriasis and the several ichthyoses, and a group of pharmacologic agents, such as Vitamin A and corticosteroids. Ultimately, we will use the clones and probes developed to determine the nucleotide sequences of keratin cDNA, and the amino acid sequences of keratin in normal and disease states. In parallel, we will investigate the glycosylation and phosphorylation of keratin and other intermediate filament proteins in the models we have noted. We will use these data to identify and localize subunits of keratins in cells and tissue from normal and pathologic epidermis. The molecular biologic and biochemical evidence developed during these investigations should lead to a definition of the function of keratin and other intermediate filament proteins and to data concerning the relationships among keratin and other cellular constitutents.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Project (R01)
Project #
5R01AR030682-06
Application #
3155866
Study Section
General Medicine A Subcommittee 2 (GMA)
Project Start
1981-07-01
Project End
1988-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
6
Fiscal Year
1986
Total Cost
Indirect Cost
Name
New York University
Department
Type
Schools of Medicine
DUNS #
004514360
City
New York
State
NY
Country
United States
Zip Code
10012
Radoja, Nada; Stojadinovic, Olivera; Waseem, Ahmad et al. (2004) Thyroid hormones and gamma interferon specifically increase K15 keratin gene transcription. Mol Cell Biol 24:3168-79
Banno, Tomohiro; Adachi, Makoto; Mukkamala, Lakshmi et al. (2003) Unique keratinocyte-specific effects of interferon-gamma that protect skin from viruses, identified using transcriptional profiling. Antivir Ther 8:541-54
Gazel, Alix; Ramphal, Patricia; Rosdy, Martin et al. (2003) Transcriptional profiling of epidermal keratinocytes: comparison of genes expressed in skin, cultured keratinocytes, and reconstituted epidermis, using large DNA microarrays. J Invest Dermatol 121:1459-68
Adachi, Makoto; Gazel, Alix; Pintucci, Giuseppe et al. (2003) Specificity in stress response: epidermal keratinocytes exhibit specialized UV-responsive signal transduction pathways. DNA Cell Biol 22:665-77
Freedberg, I M; Tomic-Canic, M; Komine, M et al. (2001) Keratins and the keratinocyte activation cycle. J Invest Dermatol 116:633-40
Komine, M; Rao, L S; Freedberg, I M et al. (2001) Interleukin-1 induces transcription of keratin K6 in human epidermal keratinocytes. J Invest Dermatol 116:330-8
Komine, M; Rao, L S; Kaneko, T et al. (2000) Inflammatory versus proliferative processes in epidermis. Tumor necrosis factor alpha induces K6b keratin synthesis through a transcriptional complex containing NFkappa B and C/EBPbeta. J Biol Chem 275:32077-88
Radoja, N; Komine, M; Jho, S H et al. (2000) Novel mechanism of steroid action in skin through glucocorticoid receptor monomers. Mol Cell Biol 20:4328-39
Khosla, S; Melton 3rd, L J; Wermers, R A et al. (1999) Primary hyperparathyroidism and the risk of fracture: a population-based study. J Bone Miner Res 14:1700-7
Tomic-Canic, M; Komine, M; Freedberg, I M et al. (1998) Epidermal signal transduction and transcription factor activation in activated keratinocytes. J Dermatol Sci 17:167-81

Showing the most recent 10 out of 46 publications