The human mast cell: Functions in physiology and disease

Citation
G. Krishnaswamy et al., The human mast cell: Functions in physiology and disease, FRONT BIOSC, 6, 2001, pp. D1109-D1127
Citations number
221
Categorie Soggetti
Biochemistry & Biophysics
Journal title
FRONTIERS IN BIOSCIENCE
ISSN journal
10939946 → ACNP
Volume
6
Year of publication
2001
Pages
D1109 - D1127
Database
ISI
SICI code
1093-9946(200109)6:<D1109:THMCFI>2.0.ZU;2-3
Abstract
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.