Figure 6
Figure 6. Src family kinases in Gq- and Gi-coupled receptor signaling. (Ai) The Gq-coupled PAR-4 signals via the activation of phospholipase β (PLCβ), which hydrolyses PI4,5P2 to the second messengers DAG and IP3, which in turn activate serine/threonine PKC and facilitate Ca2+ mobilization, respectively. The SFK Fyn associates with PKCδ downstream of PLCβ, and they reciprocally activate one another. Increased Ca2+ concentration contributes to SFK activation. SFKs lie upstream of the PI3K/Akt pathway. (Aii) PAR-4 coupled to G12/13 mediates platelet shape change via the RhoA/ROCK/MLC pathway. Fyn activated downstream of G12/13 inhibits signaling via Gq-coupled PAR-4. (B) The Gi-coupled ADP receptor P2Y12 signals by inhibiting adenylate cyclase/cAMP/protein kinase A (PKA) and Gβγ-mediated activation of PI3K/Akt. The SFKs Lyn and Fyn bind directly to the Gα subunit and play a critical role in initiating signaling via the PI3K/Akt pathway.

Src family kinases in Gq- and Gi-coupled receptor signaling. (Ai) The Gq-coupled PAR-4 signals via the activation of phospholipase β (PLCβ), which hydrolyses PI4,5P2 to the second messengers DAG and IP3, which in turn activate serine/threonine PKC and facilitate Ca2+ mobilization, respectively. The SFK Fyn associates with PKCδ downstream of PLCβ, and they reciprocally activate one another. Increased Ca2+ concentration contributes to SFK activation. SFKs lie upstream of the PI3K/Akt pathway. (Aii) PAR-4 coupled to G12/13 mediates platelet shape change via the RhoA/ROCK/MLC pathway. Fyn activated downstream of G12/13 inhibits signaling via Gq-coupled PAR-4. (B) The Gi-coupled ADP receptor P2Y12 signals by inhibiting adenylate cyclase/cAMP/protein kinase A (PKA) and Gβγ-mediated activation of PI3K/Akt. The SFKs Lyn and Fyn bind directly to the Gα subunit and play a critical role in initiating signaling via the PI3K/Akt pathway.

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