Athymic, nude (Lewis rnu/rnu) and normal (Lewis +/+) rats were used to
study the T-cell dependence of the regulation of IgE receptors and Ig
E content on mast cells in vivo. We estimated the number of IgE recept
ors and the IgE content on peritoneal mast cells using a cytofluoromet
ric technique. The secretory capacity of the mast cells was measured i
n terms of histamine release as a function of anti-IgE concentration b
y incubation with antibodies in vitro. Two groups of rats, aged 6 and
13 weeks, were examined. The mast cells of the rats belonging to the o
lder age group (both normal and athymic) had a higher total protein (e
quivalent to dry mass or size) and mediator content (heparin, histamin
e and 5-hydroxytryptamine) in accordance with previous findings. Mast
cells of the athymic rats of both age groups contained similar levels
of IgE receptors and IgE and did not differ in these respects from tho
se of the normal rats. Of the IgE receptors available for binding, abo
ut 80% were occupied by IgE in mast cells of normal and of athymic rat
s in both age groups. The anti-IgE-induced histamine release of the ma
st cells was, however, significantly lower in athymic rats compared to
the normal controls. A change in housing from barrier-maintained to c
onventional conditions for 2 weeks enhanced the IgE-receptor and IgE c
ontent, as well as the releasability of histamine of the mast cells of
both athymic and normal rats. The basal level of IgE occupancy of the
receptors on mast cells was therefore not impaired in the athymic rat
s, as might be inferred from previous findings of a T-cell dependence
of the IgE immune response. The results further indicate that T-lympho
cyte-derived cytokines appear not to be required for either the expres
sion of IgE receptors or for their ability to acquire IgE on mast cell
s, but such factors seem to enhance the release of histamine following
the cross-linkage of the IgE receptor on mast cells in normal conditi
ons.