COMPARATIVE ULTRASTRUCTURAL MORPHOLOGY OF HUMAN BASOPHILS STIMULATED TO RELEASE HISTAMINE BY ANTI-LGE, RECOMBINANT IGE-DEPENDENT HISTAMINE-RELEASING FACTOR, OR MONOCYTE CHEMOTACTIC PROTEIN-1
Am. Dvorak et al., COMPARATIVE ULTRASTRUCTURAL MORPHOLOGY OF HUMAN BASOPHILS STIMULATED TO RELEASE HISTAMINE BY ANTI-LGE, RECOMBINANT IGE-DEPENDENT HISTAMINE-RELEASING FACTOR, OR MONOCYTE CHEMOTACTIC PROTEIN-1, Journal of allergy and clinical immunology, 98(2), 1996, pp. 355-370
An ultrastructural analysis of human basophils stimulated with anti-Ig
E, recombinant histamine-releasing factor (rHRF), or monocyte chemotac
tic protein-1 (MCP-1) (compared with unstimulated cells) was performed
. Partially purified peripheral blood basophils were prepared for elec
tron microscopy at time points known to precede histamine release and
at half-maximum histamine release times for each secretagogue. Activat
ion morphologies associated with stimulation included granule-vesicle
attachments, piecemeal degranulation, anaphylactic degranulation, and
uropod formation. These features were qualitatively similar in the sti
mulated samples. Quantitative differences were evident, however, when
stimulated samples were compared with controls or at different time po
ints after stimulation with a single agent or when individual secretag
ogues were compared. All stimulated samples differed quantitatively fr
om the control samples. Rank orders for morphologic activation events
revealed that the most effective trigger for anaphylactic degranulatio
n was anti-IgE>MCP-1>rHRF, whereas the most effective trigger for urop
od formation was rHRF>anti-IgE>MCP-1. Rank orders for piecemeal degran
ulation and granule-vesicle attachments were the same: MCP-1>anti-IgE>
rHRF. Important relationships among these anatomic events reveal that
the development of motile configurations is not associated with the de
velopment of secretion morphologies and that piecemeal degranulation p
recedes and is inversely related to anaphylactic degranulation in stim
ulated samples.