Cutaneous application of alpha-methylspermidine activates the growth of resting hair follicles in mice

Authors: 
Fashe TM, Keinänen TA, Grigorenko NA, Khomutov AR, Jänne J, Alhonen L, Pietilä M.
Institution: 
A.I. Virtanen Institute for Molecular Sciences, Biocenter Kuopio, University of Kuopio
Country: 
Finland
Year: 
2010
Journal Name: 
Amino Acids

Recent studies using transgenic animals have revealed a crucial role for polyamines in the development and the growth of skin and hair follicles. In mammals, the growth of hair is characterized by three main cyclic phases of transformation, including a rapid growth phase (anagen), an apoptosis-driven regression phase (catagen) and a relatively quiescent resting phase (telogen). The polyamine pool during the anagen phase is higher than in telogen and catagen phases. In this study, we used alpha-methylspermidine, a metabolically stable polyamine analog, to artificially elevate the polyamine pool during telogen. This manipulation was sufficient to induce hair growth in telogen phase mice after 2 weeks of daily topical application. The application site was characterized by typical features of anagen, such as pigmentation, growing hair follicles, proliferation of follicular keratinocytes and upregulation of beta-catenin. The analog penetrated the protective epidermal layer of the skin and could be detected in dermis. The natural polyamines were partially replaced by the analog in the application site. However, the combined pool of natural spermidine and alpha-methylspermidine exceeded the physiological spermidine pool in telogen phase skin. These results highlight the role of polyamines in hair cycle regulation and show that it is possible to control the process of hair growth using physiologically stable polyamine analogs.

Tissue Type: 
Epidermal
Tissue Info: 

Fetal primary keratinocytes of C57BL/6 mice

Species: 
Mouse
CELLnTEC Products: 
Product Use: 

Isolation and cultivation for studying the effect of alpha-MeSpd on proliferation and differentiation using thymidine incorporation assay

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