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. Author manuscript; available in PMC: 2011 Mar 14.
Published in final edited form as: J Cell Sci. 2007 May 15;120(Pt 11):1944–1952. doi: 10.1242/jcs.03455

Fig. 4.

Fig. 4

Effect of γ-secretase inhibition on basal and BFT-induced cell proliferation. Cell proliferation in parental HT29/C1 cells and TCF dominant negative HT29/C1 cells (HT29/C1::TcfΔN31). Cell lines were treated with BFT (5 nM) alone or in the presence of the γ-secretase inhibitor, L685,458 (1.5 μM). Results are depicted as changes in the percentage uptake of [3H]thymidine compared with control cells for each cell line. BFT induces a significant increase in HT29/C1 cell proliferation in both parental and TCF dominant negative HT29/C1 cell lines (lanes 1 or 4, P<0.001 for both cell lines vs. control) that is unaltered by L685,458 (comparisons lanes 1 vs 3 and lanes 4 vs 6, P=NS). By contrast, L685,458 inhibits parental HT29/C1 cell proliferation (lane 2, P<0.001) that is ablated in TCF dominant negative HT29/C1 cells (lane 5, P<0.01 compared with lane 2) indicating γ-secretase regulation of parental HT29/C1 cell proliferation is dependent on β-catenin/TCF nuclear signaling. Data are means ± s.d. of 3–4 experiments conducted with 3–5 replicates per experiment.