The development and application of simple and selective fluorescent methods
for routine detection of mast cells are of considerable interest because t
hese cells play an important role in health and disease. In the present stu
dy, aspects of staining of sulfated glycosaminoglycans with carbocyanines,
aryloxazoles, and a ruthenium(II) complex are discussed. The most suitable
of these compounds for visualizing mast cells in smears and tissue sections
are DiOC(1)(3), Q-dmPOPOP, PyPO, and Rubipy, which have been practically o
verlooked as cationic fluorochromes for fixed cells. Bicolour fluorescence
allowing simultaneous observation of mast cells and other cell types and ti
ssue components by application of these dyes in combination with haematoxyl
in and/or eosin, or by counterstaining with other fluorochromes or fluoresc
ent complexes is particularly useful for routine histopathological studies.
Simple and reliable staining procedures, bright emission, high sensitivity
and stability, permanent mounting, and possibilities for combined use with
other histochemical methods are the most relevant advantages of these mast
cell fluorochromes.