Fig. 3.
Fig. 3. Demonstration of the presence of TAFI in rabbit plasma. (A) The concentration-dependent potentiation of lysis time by the carboxypeptidase inhibitor from the potato (PTI). Lysis times were determined using a turbidometric assay as indicated in Materials and Methods. The inset represents a Western blot of purified human TAFI, human plasma, and rabbit plasma in lanes A, B, and C, respectively. (B) The concentration-dependent potentiation of lysis time by the factor Xa inhibitor, TAP. Clots were formed as indicated in Materials and Methods, but with 294 pmol/L tPA. The effect of various concentrations of TAP (0 to 10 μmol/L) on lysis time was determined for clots produced in the absence (○) or presence (•) of 5 μg/mL PTI. Indicated values are the average from 2 experiments, in which the range did not exceed 5% of the mean. These data indicate that rabbit plasma contains TAFI, which, when activated by thrombin, is able to prolong lysis time and is inhibited by the carboxypeptidase inhibitor PTI.

Demonstration of the presence of TAFI in rabbit plasma. (A) The concentration-dependent potentiation of lysis time by the carboxypeptidase inhibitor from the potato (PTI). Lysis times were determined using a turbidometric assay as indicated in Materials and Methods. The inset represents a Western blot of purified human TAFI, human plasma, and rabbit plasma in lanes A, B, and C, respectively. (B) The concentration-dependent potentiation of lysis time by the factor Xa inhibitor, TAP. Clots were formed as indicated in Materials and Methods, but with 294 pmol/L tPA. The effect of various concentrations of TAP (0 to 10 μmol/L) on lysis time was determined for clots produced in the absence (○) or presence (•) of 5 μg/mL PTI. Indicated values are the average from 2 experiments, in which the range did not exceed 5% of the mean. These data indicate that rabbit plasma contains TAFI, which, when activated by thrombin, is able to prolong lysis time and is inhibited by the carboxypeptidase inhibitor PTI.

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