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Usage Information

Coagulation factor VA2440G causes east Texas bleeding disorder via TFPIα
Lisa M. Vincent, … , Dianna M. Milewicz, Björn Dahlbäck
Lisa M. Vincent, … , Dianna M. Milewicz, Björn Dahlbäck
Published August 27, 2013
Citation Information: J Clin Invest. 2013;123(9):3777-3787. https://doi.org/10.1172/JCI69091.
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Research Article

Coagulation factor VA2440G causes east Texas bleeding disorder via TFPIα

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Abstract

The autosomal dominantly inherited east Texas bleeding disorder is linked to an A2440G variant in exon 13 of the F5 gene. Affected individuals have normal levels of coagulation factor V (FV) activity, but demonstrate inhibition of global coagulation tests. We demonstrated that the A2440G mutation causes upregulation of an alternatively spliced F5 transcript that results in an in-frame deletion of 702 amino acids of the large activation fragment, the B domain. The approximately 250-kDa FV isoform (FV-short), which can be fully activated by thrombin, is present in all A2440G carriers’ plasma (n = 16). FV-short inhibits coagulation through an indirect mechanism by forming a complex with tissue factor pathway inhibitor-α (TFPIα), resulting in an approximately 10-fold increase in plasma TFPIα, suggesting that the TFPIα:FV-short complexes are retained in circulation. The TFPIα:FV-short complexes efficiently inhibit thrombin generation of both intrinsic and extrinsic coagulation pathways. These data demonstrate that the east Texas bleeding disorder–associated F5A2440G leads to the formation of the TFPIα:FV-short complex, which inhibits activation and propagation of coagulation.

Authors

Lisa M. Vincent, Sinh Tran, Ruzica Livaja, Tracy A. Bensend, Dianna M. Milewicz, Björn Dahlbäck

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Usage data is cumulative from May 2024 through May 2025.

Usage JCI PMC
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PDF 93 46
Figure 528 2
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Citation downloads 75 0
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Total Views 1,528
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