Membrane-bound stem cell factor is the major but not only driver of fibroblast-induced murine skin mast cell differentiation.
Mandy LeistCathleen Annett SünderSebastian DrubeCarolin ZimmermannAstrid GeldmacherMartin MetzAnne DudeckMarcus MaurerPublished in: Experimental dermatology (2017)
The maintenance and modulation of cutaneous mast cell (MC) numbers is held to be important for skin immune responses to allergens and pathogens. The increase in MC numbers in the skin is achieved by proliferation and the differentiation of precursor to mature MCs. Fibroblast-derived SCF is thought to be the major skin MC growth factor and it potently induces MC proliferation. The mechanisms of fibroblast-induced skin MC differentiation, including the role of SCF, however, remain insufficiently characterized and understood. Using cocultures of immature murine MCs and fibroblasts, we found that the adhesion of immature MCs to fibroblasts via VCAM-1 and α4 β7 integrin is very important for subsequent differentiation, which is driven by fibroblast membrane-bound SCF and additional fibroblast-derived membrane-bound signals. Thus, our results show that fibroblast-induced MC differentiation is induced by direct cell-cell contact and involves both Kit-dependent and Kit-independent pathways. Our findings add to the understanding of how immature mast cells mature in murine skin and encourage further analyses of the underlying mechanisms, which may result in novel targets for the modulation of skin mast cell driven diseases.
Keyphrases
- wound healing
- soft tissue
- growth factor
- stem cells
- immune response
- diabetic rats
- single cell
- cell therapy
- drug induced
- escherichia coli
- toll like receptor
- mesenchymal stem cells
- staphylococcus aureus
- inflammatory response
- multidrug resistant
- dendritic cells
- bone marrow
- extracellular matrix
- candida albicans
- biofilm formation
- cell adhesion