Mast cells are multifunctional, tissue-dwelling cells capable of secreting
a wide variety of mediators. They develop from bone marrow-derived progenit
or cells, primed with stem cell factor (SCF), which mediates its actions by
interacting with the SCF receptor or c-kit on the cell surface. Mast cells
continue their maturation and differentiation in peripheral tissue, develo
ping into two well described subsets of cells, MCT and MCTC cells, varying
in content of tryptase and chymase as well as in immunobiology. Mast cells
are activated by numerous stimuli, including antigen (acting via the high a
ffinity IgE receptor, Fc epsilon RI), superoxides, complement proteins, neu
ropeptides and lipoproteins resulting in activation and degranulation. Foll
owing activation, these cells express mediators such as histamine, leukotri
enes and prostanoids, as well as proteases, and many cytokines and chemokin
es, pivotal to the genesis of an inflammatory response. Recent data suggest
s that mast cells may play an active role in such diverse diseases as ather
osclerosis, malignancy, asthma, pulmonary fibrosis and arthritis. Mast cell
s directly interact with bacteria and appear to play a vital role in host d
efense against pathogens. Drugs, such as glucocorticoids, cyclosporine and
cromolyn have been demonstrated to have inhibitory effects on mast cell deg
ranulation or mediator release.