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Related Concept Videos

Extrinsic and Intrinsic Pathways of Hemostasis01:20

Extrinsic and Intrinsic Pathways of Hemostasis

Blood clotting or coagulation involves extrinsic and intrinsic pathways, which ultimately merge into the common pathway, forming a fibrin clot.
The Extrinsic Pathway
The extrinsic pathway of coagulation is typically initiated by tissue damage that exposes blood to tissue factor (TF), a protein released by the damaged tissue cells outside the blood vessels—this interaction with TF triggers biochemical reactions involving specific clotting factors. The key player here is Factor VII, which forms a...

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Related Experiment Video

Updated: May 11, 2026

Extracellular Vesicle Tissue Factor Activity Assay
03:53

Extracellular Vesicle Tissue Factor Activity Assay

Published on: December 29, 2023

Analysis of tissue factor expression in various cell model systems: cryptic vs. active.

H Kothari1, U R Pendurthi, L V M Rao

  • 1Department of Cellular and Molecular Biology, Center for Biomedical Research, The University of Texas Health Science Center at Tyler, TX 75708, USA.

Journal of Thrombosis and Haemostasis : JTH
|April 30, 2013
PubMed
Summary
This summary is machine-generated.

Tissue factor (TF) encryption is common across cell types, with most TF existing in an inactive, cryptic form. Cell activation increases TF activity by converting cryptic TF to its active state, not by enhancing existing active TF.

Keywords:
blood coagulation factorscellsfactor VIIahemostasisphospholipidstissue factor

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Last Updated: May 11, 2026

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Published on: December 29, 2023

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Published on: February 14, 2017

Area of Science:

  • Biochemistry
  • Cell Biology
  • Hematology

Background:

  • Tissue factor (TF) encryption regulates its coagulant activity.
  • Understanding TF encryption mechanisms has been hindered by varied experimental models.

Purpose of the Study:

  • Characterize TF procoagulant activity across different cell types.
  • Determine if increased TF activity upon activation results from cryptic TF transformation.

Main Methods:

  • Kinetic analyses of TF-FVIIa activation and FVIIa binding.
  • Utilized fibroblast, cancer, endothelial, and monocytic cell models.
  • Estimated TF coagulant-specific activity and cryptic/active TF percentages.

Main Results:

  • MDA-231 and WI-38 cells express significantly more TF than HUVEC and THP-1 cells.
  • TF-specific activity was similar across MDA-231, WI-38, and THP-1 cells.
  • 80-90% of TF in MDA-231, WI-38, and THP-1 cells was cryptic; activation increases activity via decryption.

Conclusions:

  • TF encryption is not cell-type specific.
  • The majority of TF in cancer cells is not constitutively procoagulant.
  • Cell activation enhances TF procoagulant activity through decryption of cryptic TF.