A murine model of factor XI deficiency.

Gailani D, Lasky NM, Broze GJ
Blood Coagul Fibrinolysis. 1997 8 (2): 134-44

PMID: 9518045 · DOI:10.1097/00001721-199703000-00008

To facilitate investigations into the physiologic and pathologic roles of factor XI, we have developed a murine model of severe factor XI deficiency using the technique of homologous recombination in embryonic stem cells. The factor XI gene was disrupted by introducing a neomycin phosphotransferase gene into the fifth exon. The activated partial thromboplastin times of homozygous null mice were prolonged (158- > 200 s) compared with wild type (25-34 s) and heterozygous null (40-61 s) litter mates. Factor XI activity was absent from the plasma of mice homozygous for the null mutation and factor XI mRNA was undetectable by Northern blot and reverse transcription/PCR in the livers of homozygous null animals. The genotypes of progeny from matings of mice heterozygous for the factor XI null allele followed the expected Mendelian ratio (1:2:1, wild type 26%, heterozygote null 54%, homozygous null 20%), indicating that severe factor XI deficiency did not result in increased intrauterine death. Results of a tail transection bleeding time assay were similar for wild type and homozygous null animals with, at most, a tendency for slightly prolonged bleeding in the homozygous null animals. The factor XI deficient mice are a unique tool for evaluating the role of factor XI in normal hemostasis and pathologic coagulation.

MeSH Terms (13)

Animals Bleeding Time Cells, Cultured Disease Models, Animal Factor XI Factor XI Deficiency Gene Targeting Liver Mice Partial Thromboplastin Time Prothrombin Time RNA, Messenger Stem Cells

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