Figure 2.
Proposed model for the role of Ca2+signaling in the commitment to becoming procoagulant. Platelet activators trigger an initial increase in [Ca2+]cyt that varies between platelets (1). This action will lead to variation in [Ca2+]mito (2), putting some above the threshold for mPTP opening. A supramaximal [Ca2+]cyt signal is triggered in these platelets (3), committing them to becoming procoagulant. Variation in the initial [Ca2+]cyt is therefore converted into 2 distinct subpopulations with distinct [Ca2+]cyt signals, leading to an all-or-nothing commitment to becoming procoagulant.

Proposed model for the role of Ca2+signaling in the commitment to becoming procoagulant. Platelet activators trigger an initial increase in [Ca2+]cyt that varies between platelets (1). This action will lead to variation in [Ca2+]mito (2), putting some above the threshold for mPTP opening. A supramaximal [Ca2+]cyt signal is triggered in these platelets (3), committing them to becoming procoagulant. Variation in the initial [Ca2+]cyt is therefore converted into 2 distinct subpopulations with distinct [Ca2+]cyt signals, leading to an all-or-nothing commitment to becoming procoagulant.

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