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. 2002 Aug;129(2):359–369. doi: 10.1046/j.1365-2249.2002.01812.x

Fig. 6.

Fig. 6

Apoptosis-inducing activities of recombinant wild-type and mutant FasL proteins secreted by COS cells. COS cells were transfected with pME18S empty vector, pME18S carrying the full-length human FasL cDNA, or FasL constructs carrying point mutants. The culture supernatants were recovered 52 h after transfection and assayed for sFasL by ELISA. Cytotoxic activity of the mutant sFasL was determined per ng of protein. Fas-expressing Jurkat-NU cells were cultured with the supernatants containing wild-type and mutant sFasL proteins for 24 h. Cell death was then estimated by DNA staining with PI. Data shown are representative of three independent experiments. ▪, Soluble FasL 0 ng/ml; Inline graphic, 0·8 ng/ml; Inline graphic, 1·6 ng/ml; Inline graphic, 3·2 ng/ml.