Skip to main content
. Author manuscript; available in PMC: 2009 Nov 1.
Published in final edited form as: Immunity. 2008 Nov;29(5):771–781. doi: 10.1016/j.immuni.2008.08.018

Figure 2. The contact-dependent inhibitory role of Tregs on MCs degranulation depends on Tregs OX40 expression and requires OX40L on BMMCs.

Figure 2

(A) BMMCs sensitized with mouse IgE anti-DNP (IgE) and challenged with Ag (IgE/Ag) in the absence or presence of equal amount of WT or OX40−/− CD4+CD25+ Tregs or separated by a transwell membrane (Transwell) were then examined for release of β-hexosaminidase. (B) Same as (A), but BMMCs were obtained from WT or OX40L−/−mice and co-cultured with WT CD4+CD25+ Tregs. Shown are the means ± SD of three independent experiments, each performed in duplicate. (C) IgE-sensitized BMMCs were challenged with Ag in the absence or presence of membranes from K562 cells expressing OX40 (K562-OX40) or empty vector (K562). (D) IgE-sensitized BMMCs were challenged with Ag in presence of Tregs, plus blocking anti-OX40L (clone MGP34) or isotype control (rat IgG2c) antibodies.