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. Author manuscript; available in PMC: 2007 Oct 29.
Published in final edited form as: J Biol Chem. 2007 Jul 12;282(37):27100–27114. doi: 10.1074/jbc.M701316200

FIGURE 5. Apoptosis induced by incubating wild-type and iPLA2β-null mouse peritoneal macrophages with thapsigargin and fucoidan and effects of restoring iPLA2β expression to iPLA2β-null macrophages with a recombinant adenovirus.

FIGURE 5

A, wild-type (WT) and iPLA2β-knock-out (KO) macrophages were incubated without (Control) or with thapsigargin (thap) alone, fucoidan (Fuc) alone, or both (thap + Fuc), and percent apoptotic cells was determined as in Fig. 2. B, WT or KO macrophages were incubated (24 h) without stimuli (lightly cross-hatched bars) or were subjected to FCL (solid black bars) with Ac-LDL and ACAT inhibitor 58035, and percent apoptotic cells was determined. Checkered bar represents experiments in which iPLA2β expression was restored recombinant adenovirus encoding iPLA2β (PLA2). Other cells were infected with control (C) virus without iPLA2β coding sequence. Immunoblots for iPLA2β and tubulin (C) illustrate iPLA2β expression in macrophages infected with virus (V) versus control (C), wild-type (W), or iPLA2β-knock-out (K) cells. Mean values ± S.E. are displayed (n = 6). Asterisk denotes p < 0.05 for WT versus KO.