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. 2015 May 8;27(9):447–457. doi: 10.1093/intimm/dxv029

Fig. 1.

Fig. 1.

Slamf6 interacts with E. coli and C. rodentium. Relative luminescence measured in Jurkat cells that were transfected with a fusion construct of Slamf6 and CD3ζ and a Renilla luciferase reporter. (A) The luciferase activity of Jurkat cells after o/n stimulation with serial dilutions of heat-inactivated S. aureus, E. coli (F18) or S. typhimurium and (B) C. rodentium (DS100). (C) The luciferase activity of Jurkat cells after o/n stimulation with E. coli, E. coli ΔOmpC, E. coli ΔOmpF or double-deficient E. coli. (D) The luciferase activity of Jurkat cells after o/n stimulation in the absence and presence of anti-Slamf6 mAb (330). (E) The luciferase activity of Jurkat cells in which single mutations were made, after o/n stimulation.