Figure 2.

The IKKβ(EE)IEC small intestinal LP is infiltrated with F4/80 and CD3+ cells. (a) Frozen sections of WT or IKKβ(EE)IEC jejunum and colon were stained for the indicated markers and visualized by immunofluorescence. Representative of five experiments. (b) RNAs from WT or IKKβ(EE)IEC enterocytes were subjected to gene expression profiling using whole-genome oligonucleotide arrays (Agilent). Shown are the expression levels of chemokine genes. Positive or negative values represent fold changes between IKKβ(EE)IEC mice and littermate controls (n = 2). (c) Small intestinal IELs and LPLs were isolated from WT or IKKβ(EE)IEC mice and counted. Percentages of F4/80 and CD3+ cells were determined by flow cytometry in cells gated for CD45. Results are means ± SEM (n = 6). *, P < 0.05 versus WT. Data are representative of three independent experiments.

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