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Tissue plasminogen activator neurovascular toxicity is controlled by activated protein C

Abstract

Although thrombolytic effects of tissue plasminogen activator (tPA) are beneficial, its neurotoxicity1,2,3,4,5 is problematic. Here, we report that tPA potentiates apoptosis in ischemic human brain endothelium and in mouse cortical neurons treated with N-methyl-D-aspartate (NMDA) by shifting the apoptotic pathways from caspase-9 to caspase-8, which directly activates caspase-3 without amplification through the Bid-mediated mitochondrial pathway6. In vivo, tPA-induced cerebral ischemic injury in mice was reduced by intracerebroventricular administration of caspase-8 inhibitor, but not by caspase-9 inhibitor, in contrast to controls in which caspase-9 inhibitor, but not caspase-8 inhibitor, was protective. Activated protein C (APC), a serine protease with anticoagulant, anti-inflammatory and antiapoptotic activities7, which is neuroprotective during transient ischemia8,9 and promotes activation of antiapoptotic mechanisms in brain cells by acting directly on endothelium9,10,11 and neurons12, blocked tPA vascular and neuronal toxicities in vitro and in vivo. APC inhibited tPA-induced caspase-8 activation of caspase-3 in endothelium and caspase-3–dependent nuclear translocation of apoptosis-inducing factor in NMDA-treated neurons and reduced tPA-mediated cerebral ischemic injury in mice. Data suggest that tPA shifts the apoptotic signal in stressed brain cells from the intrinsic to the extrinsic pathway which requires caspase-8. APC blocks tPA's neurovascular toxicity and may add substantially to the effectiveness of tPA therapy for stroke.

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Figure 1: tPA toxicity to human BEC and cytoprotection by human APC.
Figure 2: tPA's apoptotic signal in hypoxic human BEC requires caspase-8 and is blocked by APC.
Figure 3: tPA shifts NMDA-induced apoptosis in mouse cortical neurons to caspase-8 which is blocked by mouse APC.
Figure 4: tPA-induced cerebral injury in a mouse stroke model and protection by mouse APC.

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Acknowledgements

This work was supported by the United States National Institutes of Health grant HL63290.

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Correspondence to Berislav V Zlokovic.

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Berislav V. Zlokovic serves as a consultant for Socratech LLC, which potentially may have interest in developing activated protein C.

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Liu, D., Cheng, T., Guo, H. et al. Tissue plasminogen activator neurovascular toxicity is controlled by activated protein C. Nat Med 10, 1379–1383 (2004). https://doi.org/10.1038/nm1122

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