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14-3-3 zeta regulates the mitochondrial respiratory reserve linked to platelet phosphatidylserine exposure and procoagulant function

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Authors

Schoenwaelder, Simone M.
Darbousset, Roxane
Cranmer, Susan L.
Ramshaw, Hayley S.
Orive, Stephanie L.
Sturgeon, Sharelle
Yuan, Yuping
Yao, Yu
Krycer, James R.
Woodcock, Joanne M.

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Macmillan Publishers Ltd

Abstract

The 14-3-3 family of adaptor proteins regulate diverse cellular functions including cell proliferation, metabolism, adhesion and apoptosis. Platelets express numerous 14-3-3 isoforms, including 14-3-3ζ, which has previously been implicated in regulating GPIbα function. Here we show an important role for 14-3-3ζ in regulating arterial thrombosis. Interestingly, this thrombosis defect is not related to alterations in von Willebrand factor (VWF)-GPIb adhesive function or platelet activation, but instead associated with reduced platelet phosphatidylserine (PS) exposure and procoagulant function. Decreased PS exposure in 14-3-3ζ -deficient platelets is associated with more sustained levels of metabolic ATP and increased mitochondrial respiratory reserve, independent of alterations in cytosolic calcium flux. Reduced platelet PS exposure in 14-3-3ζ -deficient mice does not increase bleeding risk, but results in decreased thrombin generation and protection from pulmonary embolism, leading to prolonged survival. Our studies define an important role for 14-3-3ζ in regulating platelet bioenergetics, leading to decreased platelet PS exposure and procoagulant function.

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Nature Communications

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Open Access

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