Figure 7.
Figure 7. Schematic model of intracellular communication between E-selectin receptors and PAF receptor. PAF binds to its Gq/11 protein-coupled receptor resulting in activation of PLC, leading to cleavage of PIP2 and generation of membrane-retained DAG and cytosolic IP3. DAG can directly activate TRPC6.34 Soluble InsP3 activates the IP3R on the endoplasmic reticulum to release intracellular Ca2+. These responses result in the initial rapid increase of [Ca2+]i. E-selectin interacts with E-selectin receptors on the neutrophil surface, permitting PAF-induced Ca2+ mobilization to communicate with TRPC6 and allowing permissive SOCE to occur. Modulation of this Ca2+ channel involves Src and PI 3-kinase pathways. ROC indicates receptor-operated channel; G, G protein-coupled receptor.

Schematic model of intracellular communication between E-selectin receptors and PAF receptor. PAF binds to its Gq/11 protein-coupled receptor resulting in activation of PLC, leading to cleavage of PIP2 and generation of membrane-retained DAG and cytosolic IP3. DAG can directly activate TRPC6.34  Soluble InsP3 activates the IP3R on the endoplasmic reticulum to release intracellular Ca2+. These responses result in the initial rapid increase of [Ca2+]i. E-selectin interacts with E-selectin receptors on the neutrophil surface, permitting PAF-induced Ca2+ mobilization to communicate with TRPC6 and allowing permissive SOCE to occur. Modulation of this Ca2+ channel involves Src and PI 3-kinase pathways. ROC indicates receptor-operated channel; G, G protein-coupled receptor.

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