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Mouse embryogenesis requires the tissue factor extracellular domain but not the cytoplasmic domain
Graham C.N. Parry, Nigel Mackman
Graham C.N. Parry, Nigel Mackman
Published June 1, 2000
Citation Information: J Clin Invest. 2000;105(11):1547-1554. https://doi.org/10.1172/JCI9458.
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Mouse embryogenesis requires the tissue factor extracellular domain but not the cytoplasmic domain

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Abstract

Recent studies indicate that tissue factor (TF) acts in embryogenesis, metastasis, and angiogenesis. Three independent groups showed that targeted disruption of the murine TF (mTF) gene results in 90% lethality of mTF null embryos at embryonic days 9.5–10.5. We have demonstrated that expression of wild-type human TF (hTF) from a minigene rescues the embryonic lethality of mTF null embryos. To investigate the role of TF in embryogenesis, we made mutant hTF minigenes whose products either bound FVII/VIIa at a reduced level or lacked the cytoplasmic domain. Two independent transgenic lines expressing the hTF extracellular domain mutant failed to rescue the embryonic lethality of mTF null embryos, suggesting that FVII/VIIa binding by TF, proteolytic activity by the TF/FVIIa complex, or both were required for embryogenesis. In contrast, two transgenic lines expressing the hTF cytoplasmic domain mutant rescued the embryonic lethality of mTF null embryos, indicating that the cytoplasmic domain of TF was not required for embryogenesis. We propose that TF/FVIIa-dependent extracellular protease activity is required for embryogenesis.

Authors

Graham C.N. Parry, Nigel Mackman

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Figure 2

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Expression of wild-type, mutID, and mutED minigenes in CHO cells. CHO ce...
Expression of wild-type, mutID, and mutED minigenes in CHO cells. CHO cells were transfected with 10 μg of plasmid DNA containing each of the three minigenes (WT, mutID, and mutED) or empty vector (Mock). (a) Total RNA was prepared from transfected cells and assayed for hTF mRNA expression by RT-PCR. The position of the 628-bp hTF PCR product is indicated. Primers specific for GAPDH mRNA were used as a control. A typical result from three independent experiments is shown. A higher molecular weight product (1.7 kb) was generated by amplification of contaminating genomic DNA (asterisk). (b) Expression of hTF protein in CHO cells transfected with each of the three minigenes was determined by ELISA. Results from three independent transfections are shown (mean ± SD).

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ISSN: 0021-9738 (print), 1558-8238 (online)

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Referenced in 2 patents
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