ABSTRACT
Stem cell-like keratinocytes are responsible for the high regenerative potential of the skin. For clinical applications using keratinocytes in artificial skin constructs, it is suitable to work with serum-free medium under defined conditions. This is also true for the preceding expansion of the stem cell-like keratinocyte population. Therefore, we analyzed the effect of a serum-free medium on the population distribution in comparison to an established serum-containing standard medium for keratinocyte culture. We quantified the freshly isolated as well as cultured primary human keratinocytes by their expression of the beta(1) integrin (CD29) in combination with the expression of the alpha(6) integrin (CD49f) and the transferrin receptor (CD71) by flow cytometric methods. We were able to show that cultivation with serum-free medium induces a switch of the cell population to higher expression of the beta(1) integrin. In addition, the proportion of the alpha(6)(bri)/ CD71(dim)-expressing keratinocyte cell population was enhanced about 35.4 +/- 6.56% after cultivation with serum-free medium. Culture in serum-containing medium increased this proportion of the keratinocyte cell population only about 17.3 +/- 8.06%, when compared to the alpha(6)(bri)/ CD71(dim)-expressing keratinocyte cell population measured directly after isolation. Our data show that the applied culture conditions already have an enormous impact on the development of a stem cell-like phenotype of keratinocytes. This work demonstrates that the serum-free medium significantly increases the proportion of beta(1)(bri)/alpha(6)(bri)/CD71(dim)-expressing keratinocytes. In conclusion, these findings implicate new applications in keratinocyte stem cell research and regenerative medicine.
Subject(s)
Integrin beta1/metabolism , Keratinocytes/metabolism , Stem Cells/metabolism , Antigens, CD/metabolism , Cells, Cultured , Child , Child, Preschool , Humans , Integrin alpha6/metabolism , Integrin beta1/pharmacology , Keratinocytes/cytology , Receptors, Transferrin/metabolism , Stem Cells/cytologyABSTRACT
Dermal skin-derived fibroblasts from rodent and human have been found to exhibit mesenchymal surface antigen immunophenotype and differentiation potential along the three main mesenchymal-derived tissues: bone, cartilage and fat. Human dermal skin-derived mesenchymal stem cells constitute a promising cell source in clinical applications. Therefore, we isolated fibroblastic mesenchymal stem-cell-like cells from human dermis derived from juvenile foreskins, which share a mesenchymal stem cell phenotype and multi-lineage differentiation potential. We could show similar expression patterns for CD14(-), CD29(+), CD31(-), CD34(-), CD44(+), CD45(-), CD71(+), CD73/SH3-SH4(+), CD90/Thy-1(+), CD105/SH2(+), CD133(-) and CD166/ALCAM(+) in well-established adipose tissue derived-stem cells and fibroblastic mesenchymal stem-cell-like cells by flow cytometry. Immunostainings showed that fibroblastic mesenchymal stem-cell-like cells expressed vimentin, fibronectin and collagen; they were less positive for alpha-smooth muscle actin and nestin, while they were negative for epithelial cytokeratins. When cultured under appropriate inducible conditions, both cell types could differentiate along the adipogenic and osteogenic lineages. Additionally, fibroblastic mesenchymal stem-cell-like cells demonstrated a high proliferation potential. These findings are of particular importance, because skin or adipose tissues are easily accessible for autologous cell transplantations in regenerative medicine. In summary, these data indicate that dermal fibroblasts with multilineage differentiation potential are present in human dermis and they might play a key role in cutaneous wound healing.
Subject(s)
Cell Differentiation , Fibroblasts/cytology , Mesenchymal Stem Cells/cytology , Skin/cytology , Adipocytes/cytology , Adipocytes/metabolism , Adult , Adult Stem Cells/cytology , Adult Stem Cells/metabolism , Antigens, CD/metabolism , Cell Lineage , Child, Preschool , Collagen Type I/metabolism , Cytoskeleton/metabolism , Fibroblasts/metabolism , Fibronectins/metabolism , Gene Expression , Humans , Immunohistochemistry , Intermediate Filament Proteins/metabolism , Lipoprotein Lipase/genetics , Mesenchymal Stem Cells/metabolism , Nerve Tissue Proteins/metabolism , Nestin , Osteoblasts/cytology , Osteoblasts/metabolism , Osteocalcin/metabolism , Osteonectin/metabolism , PPAR gamma/genetics , Reverse Transcriptase Polymerase Chain Reaction , Thy-1 Antigens/metabolism , Vimentin/metabolismABSTRACT
Most small-colony termites live confined within a single piece of wood on which they feed and do not possess permanent workers: Tasks are done by developmentally flexible immatures (pseudergates). By contrast, large-colony termites possess a specialized (true) worker caste and forage outside their nest for food. To shed light on possible transitional steps between these contrasting patterns of social organization, we studied an atypical Rhinotermitidae, Prorhinotermes inopinatus. In this species, despite the absence of a true worker caste, soldiers, pseudergates, and neotenic reproductives may leave the nest and explore their surroundings. Although evidence presented in this study indicates that termites recognize unknown areas, there is no directional recruitment toward them. The discovery of a food source, i.e., a piece of wood, is followed by the establishment of a long-lasting trail between the nest and the food source. A large fraction of the colony, including neotenic reproductives, ultimately migrates into the piece of wood. Our results thus demonstrate that multiple features of external foraging behavior can evolve independently of the existence of a true worker caste in termites. We suggest that large colonies with true workers, like those of most Rhinotermitidae, may easily have evolved from a Prorhinotermes-like pattern if submitted to increasing selective pressures for worker efficiency in a stable environment.