Figure 5
Figure 5. A2B adenosine receptor mediates effects of adenosine on DC differentiation. (A) Selective agonists to A1, A2A, and A3 adenosine receptors do not affect DC differentiation. Immature DCs were generated from human monocytes in the presence of the indicated concentrations of receptor-selective agonists or NECA. Agonist concentrations were 10-fold higher than their Kd for the respective receptor. Results are representative of 3 experiments. (B) Selective antagonists to A2B receptor but not to A1, A2A, or A3 adenosine receptors reverse NECA-induced alteration of DC differentiation. Immature DCs were generated from human monocytes in the presence of 100 μM NECA and selective antagonists at indicated concentrations. Antagonist concentrations were 10-fold higher than their Ki for the respective receptor. The proportion of CD14lowCD14+ cells was measured by flow cytometry. Average values from 3 different experiments are shown. Error bars denote SE. (C) Effect of NECA on cytokine secretion by DCs from mouse HPCs is not reproduced in cells from A2B−/− knockout animals. Mature DCs were generated from wild-type or A2B−/− knockout mouse HPCs with or without 100 μM NECA with 20 ng/mL TNF-α added for 24 hours for maturation. Culture supernatants from the maturation step were collected, and secreted cytokines were measured by ELISA. Average values from 3 different experiments are shown. Error bars denote SE.

A2B adenosine receptor mediates effects of adenosine on DC differentiation. (A) Selective agonists to A1, A2A, and A3 adenosine receptors do not affect DC differentiation. Immature DCs were generated from human monocytes in the presence of the indicated concentrations of receptor-selective agonists or NECA. Agonist concentrations were 10-fold higher than their Kd for the respective receptor. Results are representative of 3 experiments. (B) Selective antagonists to A2B receptor but not to A1, A2A, or A3 adenosine receptors reverse NECA-induced alteration of DC differentiation. Immature DCs were generated from human monocytes in the presence of 100 μM NECA and selective antagonists at indicated concentrations. Antagonist concentrations were 10-fold higher than their Ki for the respective receptor. The proportion of CD14lowCD14+ cells was measured by flow cytometry. Average values from 3 different experiments are shown. Error bars denote SE. (C) Effect of NECA on cytokine secretion by DCs from mouse HPCs is not reproduced in cells from A2B−/− knockout animals. Mature DCs were generated from wild-type or A2B−/− knockout mouse HPCs with or without 100 μM NECA with 20 ng/mL TNF-α added for 24 hours for maturation. Culture supernatants from the maturation step were collected, and secreted cytokines were measured by ELISA. Average values from 3 different experiments are shown. Error bars denote SE.

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