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Thromb Haemost 2022; 122(07): 1104-1114
DOI: 10.1055/a-1723-4075
Coagulation and Fibrinolysis

Knockdown and Knockout of Tissue Factor Pathway Inhibitor in Zebrafish

Revathi Raman
1   Department of Biological Sciences, University of North Texas, Denton, Texas, United States
,
Weam Fallatah
1   Department of Biological Sciences, University of North Texas, Denton, Texas, United States
,
Ayah Al Qaryoute
1   Department of Biological Sciences, University of North Texas, Denton, Texas, United States
,
Mia Ryon
1   Department of Biological Sciences, University of North Texas, Denton, Texas, United States
,
Pudur Jagadeeswaran
1   Department of Biological Sciences, University of North Texas, Denton, Texas, United States
› Author Affiliations Funding The work was supported by the funds from National Institutes of Health grants DK117384 and HL159399.
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Abstract

Tissue factor pathway inhibitor (TFPI) is an anticoagulant that inhibits factor VIIa and Xa in the blood coagulation pathways. TFPI contains three Kunitz domains, K1, K2, and K3. K1 and K2 inhibit factor VIIa and Xa, respectively. However, the regulation of TFPI is poorly studied. Since zebrafish has become an alternate model to discover novel actors in hemostasis, we hypothesized that TFPI regulation could be studied using this model. As a first step, we confirmed the presence of tfpia in zebrafish using reverse transcription polymerase chain reaction. We then performed piggyback knockdowns of tfpia and found increased coagulation activity in tfpia knockdown. We then created a deletion mutation in tfpia locus using the CRISPR/Cas9 method. The tfpia homozygous deletion mutants showed increased coagulation activities similar to that found in tfpia knockdown. Taken together, our data suggest that tfpia is a negative regulator for zebrafish coagulation, and silencing it leads to thrombotic phenotype. Also, the zebrafish tfpia knockout model could be used for reversing this thrombotic phenotype to identify antithrombotic novel factors by the genome-wide piggyback knockdown method.

Keywords

TFPI - coagulation - zebrafish - knockdown - knockout

Author Contributions

R.R. maintained zebrafish, performed knockdown, conducted whole-mount immunohistochemistry experiments, generated knockout mutants, characterized the mutants, participated in the discussion, and wrote the paper. W.F. collected plasma for mass spectrometry and performed Xa inhibition assays. A.A.Q. performed microinjections in larvae for laser-induced thrombosis. M.R. performed genotyping of the mutants. P.J. designed the research, analyzed the data, and edited the paper.


Supplementary Material



Publication History

Received: 01 March 2021

Accepted: 25 November 2021

Accepted Manuscript online:
16 December 2021

Article published online:
04 March 2022

© 2022. Thieme. All rights reserved.

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