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OX40 signaling sustains A1 expression and survival in CD8 T cells.

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posted on 2013-08-01, 03:02 authored by Fengyang Lei, Jianyong Song, Rizwanul Haque, Mohammad Haque, Xiaofang Xiong, Deyu Fang, Michael Croft, Jianxun Song

(a) Naive CD8 T cells from WT OT-I TCR transgenic mice were stimulated in vitro with T-depleted APCs and OVA peptide in the presence or absence of 10 µg/ml agonist anti-OX40 or rat IgG added on day 0 and day 2. (b) After 5 days of primary culture, live T cells were isolated and restimulated with T-depleted APCs and OVA peptide in the presence or absence of 10 µg/ml agonist anti-OX40 or rat IgG added. Data show the percentage T cell recovery, calculated based on assigning the input number of cells in each culture as 100%. Data are mean ± s.d from three experiments (p>0.05). Cell lysates were analyzed by immunoblotting for A1 and β-actin (top). Protein amounts were determined by densitometry and are shown relative to the expression in wild-type T cells treated with rat IgG on day 4 or 2 (taken as 1).

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