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Title: IgE receptor-activated calcium permeability pathway in rat basophilic leukemia cells

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5498330

When antigen-stimulated /sup 45/Ca uptake is measured in RBL cells loaded with > 3 mM quin2, re-extrusion of /sup 45/Ca is minimized and the initial rate of /sup 45/Ca uptake reflects the true unidirectional influx of Ca. This influx correlates more closely with secretion than with the number of IgE receptors aggregated by antigen. The antigen-induced permeability pathway is saturable, having a Km of about 0.7 mM and a Vmax of 0.9 nmol Ca/10/sup 6/ cells/min and it persists for at least an hour provided that receptor aggregation is maintained. The negatively charged fluorescent probe bis-oxonol is insensitive to changes in the mitochondrial membrane potential and is, therefore, a useful plasma membrane potential indicator. Antigen-stimulation of RBL cells equilibrated with bis-oxonol causes a rapid depolarization that peaks within 2-3 minutes and persists until receptor aggregates are disrupted. Antigen-induced depolarization is seen in the absence of extracellular calcium, but is almost completely abolished when both sodium and calcium are replaced by glucose. Addition of calcium restores this response even when sodium is absent. This suggests that the IgE receptor-activated permeability pathway has a similar conductance for sodium and calcium ions.

Research Organization:
Cornell Univ., Ithaca, NY
OSTI ID:
5498330
Report Number(s):
CONF-8604222-; TRN: 86-026531
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Vol. 45:3; Conference: 70. annual meeting of the Federation of American Society for Experimental Biology, St. Louis, MO, USA, 13 Apr 1986
Country of Publication:
United States
Language:
English