Epinephrine inhibits PI3K alpha via the Hippo kinases.

Lin, T.-Y.; Ramsamooj, S.; Liberatore, K.; Lantier, L.; Vasan, N.; Karukurichi, K.; Hwang, S.-K.; Kesicki, E. A.; Kastenhuber, E. R.; Wiederhold, T.; Yaron, T. M.; Zhu, M.; Ma, Y.; Paddock, M. N.; Zhang, G.; Hopkins, B. D.; McGuinness, O.; Schwartz, R. E.; Cantley, L. C.; Johnson, J. L.; Goncalves, M. D.

doi:10.1101/2022.07.19.500601

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bioRxiv · 10.1101/2022.07.19.500601

Epinephrine inhibits PI3K alpha via the Hippo kinases.

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Abstract

The phosphoinositide 3-kinase, p110, is an essential mediator of insulin signaling and glucose homeostasis. We systematically interrogated the human serine, threonine, and tyrosine kinome to search for novel regulators of p110 and found that the Hippo kinases phosphorylate and completely inhibit its activity. This inhibitory state corresponds to a conformational change of a membrane binding domain on p110, which impairs its ability to engage membranes. In human primary hepatocytes, cancer cell lines, and rodent tissues, activation of the Hippo kinases, MST1/2, using forskolin or epinephrine is associated with phosphorylation and inhibition of p110, impairment of downstream insulin signaling, and suppression of glycolysis and glycogen synthesis. These changes are abrogated when MST1/2 are genetically deleted or inhibited with small molecules. Our study reveals a novel inhibitory pathway of PI3K signaling and a previously unappreciated link between epinephrine and insulin signaling.

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Lin, T.-Y., Ramsamooj, S., Liberatore, K., Lantier, L., Vasan, N., Karukurichi, K., Hwang, S.-K., Kesicki, E. A., Kastenhuber, E. R., Wiederhold, T., Yaron, T. M., Zhu, M., Ma, Y., Paddock, M. N., Zhang, G., Hopkins, B. D., McGuinness, O., Schwartz, R. E., Cantley, L. C., Johnson, J. L., Goncalves, M. D.. 2022-07-20. Epinephrine inhibits PI3K alpha via the Hippo kinases.. https://doi.org/10.1101/2022.07.19.500601

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