Adenosine A 3 receptor-mediated regulation of p38 and extracellular-regulated kinase ERK1/2 via phosphatidylinositol-3′-kinase

• Published in: Biochemical pharmacology 2004, Vol.67 (1), p.129-134
• Main Authors: Hammarberg, Christian, Fredholm, Bertil B., Schulte, Gunnar
• Format: Article
• Language: English
• Subjects: Adenosine; CHO cells; Mitogen-activated protein kinase; Rho GTPases; Stress-activated protein kinase; Wortmannin
• ISSN: 0006-2952; 1873-2968
• DOI: 10.1016/j.bcp.2003.08.031

The adenosine A 3 receptor generally couples to the G i class of heterotrimeric G proteins, thereby decreasing cAMP levels and also mediating signaling via release of βγ subunits. Here we describe the central role of phosphatidylinositol-3′-kinase (PI3K) for adenosine A 3 receptor-induced intracellular signaling to the stress-activated protein kinase p38 and the extracellular signal-regulated protein kinases ERK1/2. We used Chinese hamster ovary cells expressing the human adenosine A 3 receptor, phospho-specific antibodies and different pharmacological tools to dissect the signaling pathways involving PI3K. The adenosine receptor agonist 5′ N-ethylcarboxamidoadenosine induced a time- and dose-dependent increase in p38 and ERK1/2 phosphorylation, two signaling pathways that appeared also to be activated in the immortalized microglia cell line N13, which expressed endogenous adenosine A 3 receptors. The 5′ N-ethylcarboxamidoadenosine-induced effects on p38 and ERK1/2 in CHO cells were blocked by pertussis toxin pretreatment and were sensitive to pharmacological inhibition of PI3K. In addition, inhibition of Rac/Cdc42, small GTPases of the Rho family, by clostridium toxin B, diminished p38 phosphorylation but did not affect ERK1/2. Furthermore, we identified the serine 727 site of signal transducer and activator of transcription STAT3 as a probable downstream target of ERK1/2, and thereby provide evidence that adenosine A 3 receptor mediated ERK1/2 activation has functional consequences.