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Bone morphogenetic protein signaling regulates size of hair follicles and modulates the expression of cell cycle-associated genes.

By A.A. Sharov, T.Y. Sharova, Andrei N. Mardaryev, A. Tommasi di Vignano, R. Atoyan, L. Weiner, Shi Yang, J.L. Brissette, G.P. Dotto and Vladimir A. Botchkarev

Abstract

NoBone morphogenetic protein (BMP) signaling is involved in the regulation of a large variety of developmental programs, including those controlling organ sizes. Here, we show that transgenic (TG) mice overexpressing the BMP antagonist noggin (promoter, K5) are characterized by a marked increase in size of anagen hair follicles (HFs) and by the replacement of zig-zag and auchen hairs by awl-like hairs, compared with the age-matched WT controls. Markedly enlarged anagen HFs of TG mice show increased proliferation in the matrix and an increased number of hair cortex and medulla cells compared with WT HFs. Microarray and real-time PCR analyses of the laser-captured hair matrix cells show a strong decrease in expression of Cdk inhibitor p27(Kip1) and increased expression of selected cyclins in TG vs. WT mice. Similar to TG mice, p27(Kip1) knockout mice also show an increased size of anagen HFs associated with increased cell proliferation in the hair bulb. Primary epidermal keratinocytes (KC) from TG mice exhibit significantly increased proliferation and decreased p27(Kip1) expression, compared with WT KC. Alternatively, activation of BMP signaling in HaCaT KC induces growth arrest, stimulates p27(Kip1) expression, and positively regulates p27(Kip1) promoter activity, thus further supporting a role of p27(Kip1) in mediating the effects of BMP signaling on HF size. These data suggest that BMP signaling plays an important role in regulating cell proliferation and controls the size of anagen HFs by modulating the expression of cell-cycle-associated genes in hair matrix KC

Topics: Bone morphogenetic protein, BMP, Noggin, proliferation, Skin, Hair follicles
Year: 2006
DOI identifier: 10.1073/pnas.0608899103
OAI identifier: oai:bradscholars.brad.ac.uk:10454/3789
Provided by: Bradford Scholars
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