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. Author manuscript; available in PMC: 2011 May 1.
Published in final edited form as: Trends Endocrinol Metab. 2010 Jan 14;21(5):294–301. doi: 10.1016/j.tem.2009.12.004

Figure 1.

Figure 1

Examples of pathways that may be activated by EP2R and EP4R. (i) Gαs may act via cAMP-gated channels to increase Ca2+ and Ca2+-dependent calcineurin signaling. Gαs may also act via (ii) cAMP to activate PKA or EPAC, leading to activation or inhibition of phosphorylation of extracellular signal-regulated kinase (ERK), a member of the mitogen-activated protein kinase (MAPK) family. (iii) Gαs may also act independently of cAMP to activate the MAPK pathway by transactivating epidermal growth factor receptor (EGFR) via Src. Potential target transcription factors include nuclear factor of activated T-cells (NFAT), cAMP-response element binding protein (CREB) and activator protein-1(AP-1).

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