Skip to main content
. Author manuscript; available in PMC: 2009 Aug 1.
Published in final edited form as: J Immunol. 2008 Aug 1;181(3):1728–1736. doi: 10.4049/jimmunol.181.3.1728

Figure 2.

Figure 2

MEHP (A) and 15d-PGJ2 (B) treatment activate caspase-3 in cultured pro/pre-B cells. Suspension cultures of BU-11 cells were treated with ethanol:DMSO (50:50, Vh, 0.1%), MEHP (150 μM) or 15d-PGJ2 (10 μM) for the times indicated. Cytoplasmic extracts were prepared and analyzed for formation of caspase-3 fragments (17 kDa) and cleaved α-fodrin (120, 150 kDa) by immunoblotting. Representative data from at least 3 independent experiments are presented.