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Human Mast Cells (Paperback)
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Human Mast Cells (Paperback)
Series: Advances in Anatomy, Embryology and Cell Biology, 114
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8 References . 95 Subject Index 101 VIII 1 Introduction Mast cells
and basophils were first described by Ehrlich (1877, 1878, 1879).
Although these cells share many functional properties, they can
readily be distinguished using morphological criteria (Dvorak
1986a; Dvorak et al. 1983a, 1983c; Galli et al. 1984). The
identification of immunoglobulin E (IgE) and high affinity IgE
receptors on mast cells and basophils was instrumental to our
understanding of the mechanisms underlying the role of these cells
in immediate hypersensitivity reactions (Ishizaka and Ishizaka
1979; Ishizaka et al. 1966, 1972, 1973; Tomioka and Ishizaka 1971).
We now know that these IgE-mediated mechanisms as well as a number
of other stimuli can cause the rapid release of many preformed
mediators of inflammation from both mast cells and basophils (Galli
et al. 1984). The most well-known of these is histamine. Potent
mediators that are not preformed are also stimulated and released
from these cells. Recently, products of arachidonic acid
metabolism, such as the prostaglandins and leukotrienes, have been
found to be generated either by the cyclooxygenase pathway or the
lipoxy- genase pathway in mast cells and basophils (Lewis and
Austen 1981, 1984; Peters et al. 1984, 1987). Detailed studies and
reviews of the biochemistry of these mediators and their
immunologically mediated reactions have been published (Lewis and
Austen 1981, 1984; Lichtenstein et al. 1979; MacGlashan et al.
1982b; Paterson et al. 1976; Peters et al. 1984, 1987). Mast cells
and basophils contain other important biochemicals.
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