Cd43 beads

Splenic B cells were purified by negative selection using CD43 beads (Miltenyi Biotec). Purified B cells were cultured in media, 10 μg/ml F(ab′)₂ fragment of anti-mouse IgM (Jackson ImmunoResearch), 10 μg/ml LPS, 5 μg/ml CpG, or 10 μg/ml Pam3CSK4 (InvivoGen) at 37 °C for the indicated times. In some experiments, the cells were pre-treated with different concentrations of the inhibitors U0126, LY294002 (Cell Signaling Technology), NSC668394, SB203580 (Calbiochem), or PS1145 (Sigma-Aldrich) for 1 hour before stimulating with LPS. Lysates were prepared and immunoblotting performed as described (9 (link), 11 (link)). All immunoblotting antibodies were from Cell Signaling Technology, except for IκB, actin (Santa Cruz Biotechnology, Inc.) and ezrin (EMD Millipore). PMA (50 ng/ml) and ionomycin (500 ng/ml) (Sigma-Aldrich) were used to stimulate B cells ex vivo 1.5 h after in vivo LPS injection. siRNAs to ezrin, MyD88, TRIF, IRF3, and control siRNAs (Dharmacon) were used at 2 μM according to manufacturer’s instructions and as described previously (14 (link)).

Resting B cells were purified by forcing spleen tissue through a 40 μm mesh into complete RPMI media (Gibco) with 6% serum. Single cell suspensions were purified by magnetic cells sorting (MACS) using CD43 beads, according to the manufacturer’s instructions (Miltenyi Biotec). Indicated cell numbers were transferred intravenously into recipient mice. To assess proliferation in vitro, resting B cells purified from tTA-H2B-mCh mice were labeled at 37 °C in 5 μM carboxyfluorescein succinimidyl ester. Labeled B cells were then stimulated with LPS and IL-4 for 72 hours as previously described^{30 (link)}. DOX was added to the cultures at 500 ng/mL.