Recently, progress has been achieved in the understanding of the morphogenic aspects of hair follicle (HF) biology; nevertheless, the molecular and genetic aspects of hair growth control remain largely unknown. Among these, the molecular pathways of HF catagen transformation are the least well understood despite the abnormalities of catagen progression underlie many common hair disorders in humans. Recent studies showed that catagen is an apoptosis-driven process and programmed-cell death is the major mechanism of catagen HF transformation. Previous studies indicated that ectopic and premature apoptosis in HF matrix is the major defect in the mutant hr/hr hairless mouse skin that causes the complete hair loss. These findings implicate the hairless (hr) gene as a key factor in coordinating basic cellular processes during HF catagen and programmed cell death as a possible key target of hr gene activity. In order to gain further insights into the molecular control of HF functions by hr, they propose the use of the native skin and cultured keratinocytes derived from the mutant (hrrh/hrrh) hairless mice as a model for elucidation the role of hr gene in regulation of apoptosis-driven catagen and for the identification of the downstream targets of hr gene activity. The hypothesized involvement of hr gene into apoptotic regulatory pathway will be tested using morphological methods, TUNEL and annexin V staining along with functional experiments (comparison of apoptosis-associated gene expression in hr/hr and wt start under UVB irradiation, treatment with DFMO and ICE and caspase-3 inhibitors). Using Northern blot analysis and immunohistochemistry, they will test the expression patterns of presumptive downstream targets of the hr-dependent regulatory pathway in wt and hr/hr skin. The search for unknown targets of hr gene activity will be performed using hybridization arrays with nucleic acids isolated from intact mouse epidermis of both hrrh/hrrh and wt genotypes. Identified candidate target genes will be prioritized according to their known role in hair follicle physiology, and also according to data obtained from functional experiments and immunohistochemical studies. Thus, the experiments outlined in this proposal are designed to dissect the cellular and molecular mechanisms of hair follicle catagen transformation using the hairless phenotype as an experimental model.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
5K01AR002204-02
Application #
6532929
Study Section
Arthritis and Musculoskeletal and Skin Diseases Special Grants Review Committee (AMS)
Program Officer
Moshell, Alan N
Project Start
2001-08-15
Project End
2006-07-31
Budget Start
2002-08-01
Budget End
2003-07-31
Support Year
2
Fiscal Year
2002
Total Cost
$123,660
Indirect Cost
Name
Columbia University (N.Y.)
Department
Dermatology
Type
Schools of Medicine
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Wondimu, Assefa; Weir, Lynda; Robertson, Douglas et al. (2012) Loss of Arnt (Hif1?) in mouse epidermis triggers dermal angiogenesis, blood vessel dilation and clotting defects. Lab Invest 92:110-24
Magnusdottir, Erna; Kalachikov, Sergey; Mizukoshi, Koji et al. (2007) Epidermal terminal differentiation depends on B lymphocyte-induced maturation protein-1. Proc Natl Acad Sci U S A 104:14988-93
Zlotogorski, Abraham; Hochberg, Ze'ev; Mirmirani, Paradi et al. (2003) Clinical and pathologic correlations in genetically distinct forms of atrichia. Arch Dermatol 139:1591-6
Panteleyev, Andrey A; Mitchell, Pamela J; Paus, Ralf et al. (2003) Expression patterns of the transcription factor AP-2alpha during hair follicle morphogenesis and cycling. J Invest Dermatol 121:13-9
Lavker, Robert M; Sun, Tung-Tien; Oshima, Hideo et al. (2003) Hair follicle stem cells. J Investig Dermatol Symp Proc 8:28-38