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Commentary Cellscience Reviews Vol 3 No 2 ISSN 1742-8130 |
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Mast Cells Dampen Immune Reactions against Transplants
- An Ever Growing List of Their Functions
Toshiaki Kawakami, Michael J. Poderycki & Yuko Kawakami
Division of Cell Biology, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, California 92037
Received 23rd September © Cellscience 2006
Mast cells are present at the body’s interface with the environment in locations such as
the skin, gastrointestinal tract, airway, and vasculature. Arising from multipotent
hematopoietic progenitors in bone marrow, mast cells normally do not mature before
leaving the bone marrow, but instead circulate through the vascular system as immature
progenitors that then complete their development peripherally within connective or
mucosal tissues (Okayama & Kawakami, 2006). These cells have been most
extensively characterized as effectors of allergic reactions. Evidence has been
generated that shows the essential or contributing role of mast cells in anaphylaxis and
asthma (Kawakami & Galli, 2002). Indeed, mast cells activated by IgE and antigen or
other stimuli secrete preformed and de novo synthesized proinflammatory mediators
such as histamine, serotonin, proteases, prostaglandins, leukotrienes, cytokines,
chemokines, free radicals, and so on (Galli et al., 2005; Metcalfe et al., 1997). Studies in
the 80’s and 90’s have extended our understanding of the role of mast cells in the
defense against certain parasites and bacteria. Recently, mast cells were also shown to
contribute to resistance against venoms produced by snakes and honeybees (Metz et
al., 2006). In addition to controlling the attack from pathogens or toxins, mast cells are
required for efficient autoimmune reactions: without mast cells animals have less
inflammation upon the induction of experimental autoimmune encephalomyelopathy
(Secor et al., 2000) and rheumatoid arthritis (Lee et al., 2002).
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