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Histochem Cell Biol ; 133(5): 567-76, 2010 May.
Article in English | MEDLINE | ID: mdl-20336308

ABSTRACT

The ability of dermal papilla (DP) cells to induce hair growth was reported in many studies. However, early stages of hair follicle development and signals that govern this process are poorly understood. Therefore, an in vitro model may be a convenient system to study epithelial-mesenchymal interactions and early stages of epidermal morphogenesis, especially in humans. To investigate the role of DP cells in epidermal morphogenesis we modified the method of isolation of DP cells from hair follicle of human scalp and developed the three-dimensional model of epidermal morphogenesis. Isolated DP cells were able to differentiate in adipogenic and osteogenic directions and retained activity of alkaline phosphatase (AP) for seven passages in culture. DP cells were able to induce tubule-like structures in three-dimensional model in vitro and to reorganize collagen matrix. Prolonged cultivation of DP cells has been a big problem because of the loss of hair follicle-inducing ability and growth activity after several passages. To solve this problem we immortalized DP cells by the transfection of the human telomerase reverse transcriptase cDNA (hTERT). Immortalized DP-hTERT cells retained AP activity and demonstrated low ability to osteogenic differentiation. The conditioned medium collected from actively proliferated cells as well as DP-hTERT cells themselves were capable to induce tubulogenesis after prolonged keratinocyte cultivation.


Subject(s)
Dermis/cytology , Hair Follicle/cytology , Hair Follicle/embryology , Keratinocytes/cytology , Morphogenesis/physiology , Adipocytes/cytology , Adipocytes/metabolism , Alkaline Phosphatase/metabolism , Cell Communication/physiology , Cell Culture Techniques , Cell Differentiation/physiology , Cell Line, Transformed , Cell Proliferation , Cell Shape , Cells, Cultured , Coculture Techniques , Collagen/metabolism , Extracellular Matrix/metabolism , Humans , Keratin-10/metabolism , Keratin-14/metabolism , Keratin-19/metabolism , Osteoblasts/metabolism , Osteonectin/metabolism , Osteopontin/metabolism , Telomerase/genetics , Transfection
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