Fig. 5.
SDF-1 modulates apoptosis-regulatory gene products in PB Inc+CD34+ cells.
PB CD34+ cells freshly purified after incubation on a plastic support (Inc+) were incubated (1 × 105 cells/mL) under apoptosis-inducing culture conditions (serum- and cytokine-free medium [IMDM]). Freshly isolated cells or cells harvested after a 72-hour incubation program were processed for intracellular detection of (A) antiapoptotic regulatory proteins (Bcl-2 and Bcl-xL) and (B) proapoptotic regulatory proteins (Bad and Bax) as indicated in “Materials and methods.” Modulation of Bcl-2 homolog protein expressions was evaluated in the absence or presence of SDF-1 (0.05 ng/mL). Data from at least 3 different donors with similar results were analyzed. Histograms from a typical donor are presented. The percentage or MFI (AU) or both of positive cells for Bcl-2, Bcl-xL, Bad, and Bax are shown within the histograms. The left-hand histogram represents the negative control (IgG).