β-Catenin and Hedgehog Signal Strength Can Specify Number and Location of Hair Follicles in Adult Epidermis without Recruitment of Bulge Stem Cells

• Published in: Developmental cell Vol. 9; no. 1; pp. 121 - 131
• Main Authors: Silva-Vargas, Violeta, Lo Celso, Cristina, Giangreco, Adam, Ofstad, Tyler, Prowse, David M., Braun, Kristin M., Watt, Fiona M.
• Format: Journal Article
• Language: English
• Published: Cambridge, MA Elsevier Inc 01.07.2005; Cell Press
• Subjects: Animals; beta Catenin; Biological and medical sciences; Cell Differentiation; Cell differentiation, maturation, development, hematopoiesis; Cell physiology; Cytoskeletal Proteins - genetics; Cytoskeletal Proteins - metabolism; Epidermis - cytology; Epidermis - drug effects; Epidermis - metabolism; Female; Fundamental and applied biological sciences. Psychology; Gene Dosage; Hair Follicle - cytology; Hair Follicle - drug effects; Hair Follicle - metabolism; Hedgehog Proteins; Keratinocytes - cytology; Keratinocytes - drug effects; Keratinocytes - metabolism; Mice; Mice, Transgenic; Molecular and cellular biology; Oligonucleotide Array Sequence Analysis; Sebaceous Glands - cytology; Sebaceous Glands - drug effects; Sebaceous Glands - metabolism; Signal Transduction; Stem Cells - cytology; Stem Cells - drug effects; Stem Cells - metabolism; Tamoxifen - analogs & derivatives; Tamoxifen - pharmacology; Trans-Activators - genetics; Trans-Activators - metabolism; Transgenes; Human; Stem cell; Development; Adult; Epidermis; Hair follicle; Catenin
• ISSN: 1534-5807; 1878-1551
• DOI: 10.1016/j.devcel.2005.04.013

Using K14ΔNβ-cateninER transgenic mice, we show that short-term, low-level β-catenin activation stimulates de novo hair follicle formation from sebaceous glands and interfollicular epidermis, while only sustained, high-level activation induces new follicles from preexisting follicles. The Hedgehog pathway is upregulated by β-catenin activation, and inhibition of Hedgehog signaling converts the low β-catenin phenotype to wild-type epidermis and the high phenotype to low. β-catenin-induced follicles contain clonogenic keratinocytes that express bulge markers; the follicles induce dermal papillae and provide a niche for melanocytes, and they undergo 4OHT-dependent cycles of growth and regression. New follicles induced in interfollicular epidermis are derived from that cellular compartment and not through bulge stem cell migration or division. These results demonstrate the remarkable capacity of adult epidermis to be reprogrammed by titrating β-catenin and Hedgehog signal strength and establish that cells from interfollicular epidermis can acquire certain characteristics of bulge stem cells.