The long-term goal of this proposal is to understand the regulation of epithelial stem cell commitment to the sebaceous gland lineage. The sebaceous gland develops along with the hair follicle as epidermal stem cells commit to a particular lineage and differentiate. When sebaceous development is aberrant, two unsolved dermatological pathologies, acne vulgaris and human tumors, develop. Yet, despite the clinical importance of this cell lineage in human disease, little Is known about how this lineage forms. My prelimary data identifies a population of unipotent progenitor cells that by expression of the transcriptional repressor, Blimpl, regulates the cellular Input into the sebaceous gland and elicits premature activity of epithelial stem cells. The central hypothesis tested by this proposal is that the formation of sebaceous progenitors from hair follicle stem cells is crucial for proper formation and biology of the sebaceous gland. This hypothesis will be tested in this grant application by experiments: 1) identifying mechanisms that regulate progenitor fate by Blimpl, and 2) determining the role of sebaceous progenitors in communication with the hair follicle stem cell compartment. During the mentored phase of this award, I have identified a number of potential mechanisms that regulate sebaceous gland developoment and will follow-up on particular genes identified and cellular mechanisms will be performed in the independent phase of this proposal. Data generated from the proposed experiments will advance our understanding of the mechanisms regulating sebaceous gland development and and stem cell lineage commitment in the skin. In addition, these proposed studies will potentially lead to the development of therapeutic treatments for disorders of the sebaceous gland as well as other skin disorders and cancers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Transition Award (R00)
Project #
5R00AR054775-05
Application #
8011731
Study Section
Special Emphasis Panel (NSS)
Program Officer
Baker, Carl
Project Start
2009-04-01
Project End
2011-12-31
Budget Start
2011-01-01
Budget End
2011-12-31
Support Year
5
Fiscal Year
2011
Total Cost
$236,766
Indirect Cost
Name
Yale University
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Goldstein, Jill; Horsley, Valerie (2012) Home sweet home: skin stem cell niches. Cell Mol Life Sci 69:2573-82
Festa, Eric; Fretz, Jackie; Berry, Ryan et al. (2011) Adipocyte lineage cells contribute to the skin stem cell niche to drive hair cycling. Cell 146:761-71
Fuchs, Elaine; Horsley, Valerie (2011) Ferreting out stem cells from their niches. Nat Cell Biol 13:513-8
Horsley, Valerie (2009) Epigenetics, Wnt signaling, and stem cells: the Pygo2 connection. J Cell Biol 185:761-3