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. Author manuscript; available in PMC: 2008 Nov 25.
Published in final edited form as: Eur J Immunol. 2008 Jul;38(7):1988–1998. doi: 10.1002/eji.200737738

Figure 1.

Figure 1

Reciprocal effects of Gαi2 and Gαi3 on GVHD development. SCID BALB/c mice were each administrated intraperitoneally with 107 T cells isolated from WT, Gαi2−/−, and Gαi3−/− mice on 129Sv/C57BL/6 background. Animals were monitored for weight (A) and survival (B) weekly. Note: significant acceleration of GVHD-associated morbidity in recipient of Gαi3−/− T cells (**p<0.01) and reduction of the disease in recipient of Gαi2−/− T cells (*p<0.05) as compared to mice receiving WT T cells. Results are from three (Gαi3−/− T cells) or four (Gαi2−/− T cells) independent experiments with 7∼12 mice per group in each experiment. The total number of mice was 31, 28 and 30 receiving WT, Gαi2−/− and Gαi3−/− T cells, respectively. Mean ± SD of weight changes relative to day 0 is shown in (A) (*p<0.05).