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. Author manuscript; available in PMC: 2013 Oct 1.
Published in final edited form as: Clin Immunol. 2012 Aug 4;145(1):82–88. doi: 10.1016/j.clim.2012.07.015

Table 1.

Sf double mutant trafficking receptor gene expression and its effect on skin and lung inflammation: Lack of skin and lung inflammation in Sf.II2−/− mice correlates with lack of increased expression of Th2 related trafficking receptor genes. Liver inflammation is representative of systemic inflammation that includes inflammation in the colon, pancreas and salivary glands.*

Strain TRG expression Liver inflammation Lung inflammation Skin inflammation
Th1-related Th2-related
B6 1 1 0 0 0
Sf** 3 3 3 4 4
Sf.Il2−/− 3 1 3 1 0
Sf.Il4−/− 4 2 4 4 4
Sf.Ifng−/− (6 wk) 2 3 3 3 3
Sf.Stat6−/− 4 2 4 4 4
Sf.Itgae−/− 3 3 3 2 1
Sf.Ltb4r1−/− 3 3 3 3 2
Sf.Alox5−/− 3 4 4 4 4
Sf.Il10−/− ND ND 4 4 4
Sf.Cx3cr1gfp/gfp ND ND 3 4 4
Sf.Fas−/− (12 wk) ND ND 3 4 4
*

Trafficking receptor gene expression was determined by quantitative PCR and microarray assays [4,67]. Inflammation of individual organs was determined by histology and visual examination of the skin. Mice are examined at 3–4 weeks of age. ND: not determined. An arbitrary assignment of “1” for trafficking receptor expression is given to B6 mice as a reference..

**

Sf, Scurfy and Fox P3 deficient; Ifng, Interferon-γ; Itgae, integrin αE; Ltb4r1, leukotriene B4 receptor 1; Alox5, arachidonate 5-lipoxygenase; Cx3cr1gfp/gfp, Cx3cr1 deficient and expression of EGFP under control of endogenous Cx3cr1 locus.