Figure 2
Figure 2. Induction of SHIP deficiency expands the CD25+FoxP3+ Treg compartment in peripheral lymphoid organs. Spleen and mesenteric LN of polyI/C-treated MxCreSHIPflox/flox (Cre+, n = 6) and SHIPflox/flox (Cre−, n = 9) were harvested and processed into single-cell suspensions. Frequency and absolute numbers of CD4+CD25+FoxP3+ Tregs were assessed by flow cytometry, as described in Figure 1. (A) Representative CD4 versus CD25 staining in spleen and LN from MxCreSHIPflox/flox and SHIPflox/flox mice after poly(I/C) administration. (B) Percentage frequency of CD4+CD25+FoxP3+ Tregs after gating on CD3+ T cells, and total absolute CD3+CD4+CD25+FoxP3+ Treg numbers in the spleen and LN of the indicated genotype. *P < .05. **P < .01. ***P < .001.

Induction of SHIP deficiency expands the CD25+FoxP3+ Treg compartment in peripheral lymphoid organs. Spleen and mesenteric LN of polyI/C-treated MxCreSHIPflox/flox (Cre+, n = 6) and SHIPflox/flox (Cre, n = 9) were harvested and processed into single-cell suspensions. Frequency and absolute numbers of CD4+CD25+FoxP3+ Tregs were assessed by flow cytometry, as described in Figure 1. (A) Representative CD4 versus CD25 staining in spleen and LN from MxCreSHIPflox/flox and SHIPflox/flox mice after poly(I/C) administration. (B) Percentage frequency of CD4+CD25+FoxP3+ Tregs after gating on CD3+ T cells, and total absolute CD3+CD4+CD25+FoxP3+ Treg numbers in the spleen and LN of the indicated genotype. *P < .05. **P < .01. ***P < .001.

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