Publication: Mast cell granule composition
and tissue location - a close correlation
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Date
2000
Authors
Beil, W. J. ; Schulz, M. ; Wefelmeyer, U.
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Publisher
F. Hernández y Juan F. Madrid. Universidad de Murcia: Departamento de Biología Celular e Histología
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DOI
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info:eu-repo/semantics/article
Description
Abstract
This review provides a survey on mast cell
heterogeneity, with aspects differing in humans and
rodents or which are subject of conflicting evidence
being discussed in greater detail. Mast cell subsets have
been first defined in rats by their fixation and dyebinding properties, and detailed studies in humans and
pigs reveal very similar observations. The dye-binding
properties of rat mast cell subsets are causally related to
the absence or presence of heparin in their granules. In
humans, this relation has not been shown. Rodent mast
cell subsets store different chymase-isoforms. In
contrast, just a single chymase has been defined in
humans, and mast cells are classified by the presence or
relative absence of this chymase. Different investigators
find quite different proportions of chymase-positive to
chymase-negative mast cells. Tryptase(s) are found in
most or every human mast cell, but in rodents, they have
hitherto been essentially localised to mast cells in
connective tissues. Human mast cell subsets may also be
defined by their expression of receptors such as CSaR
and possibly the B-chemokine receptor CCR3; the CCR3
expression seems to be related to the human mast cell
chymase expression. Ultrastructural studies are helpful
to distinguish human mast cell subsets, and allow to
distinguish between chronic and acute activation.
The phenotypical characteristics may change in
association with inflammation or other disease
processes. Studies in humans and pigs show changed
dye-binding and fixation properties of the granules.
Experimental rodent infection models reveal similar
changes of chymase isoform expression. Human lung
mast cells have been reported to strongly upregulate
their chymase content in pulmonary vascular disease.
This line of evidence can explain some inconsistent
information on mast cell heterogeneity and may help to
understand the physiological role of mast cells.
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Citation
Histology and Histopathology, Vol. 15, n.º 3 (2000)
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