Figure 2.
Figure 2. FVIII in plasma and platelets in 2bF8-transgenic mice. Transgenic mice were developed with the cDNA for B domain-deleted FVIII placed under the control of the integrin α-IIb promoter and bred onto the murine FVIIInull background. These transgenic mice (2bF8) only expressed FVIII in megakaryocytes and stored FVIII together with VWF in platelets. (A) Plasma FVIII was measured and was present in wild-type (WT), but was absent in plasma from either FVIIInull or 2bF8 transgenic (FVIIInull) mice. (B) Platelet FVIII was measured in murine platelets and was absent in wild-type and FVIIInull mice; but, in 2bF8 transgenic mice, platelet FVIII was present and was greater in homozygous transgenic mice (2bF8trans+/+) than in heterozygous (2bF8trans+/–) mice. To determine the effect of VWF on the expression of FVIII in platelets, the 2bF8 transgene was bred onto the double KO background (FVIIInull VWFnull). Platelet FVIII expression was reduced in the absence of VWF. Bone marrow transplantation (BMT) from a heterozygous 2bF8 mouse conferred similar expression levels when transplanted into FVIIInull mice following ablative bone marrow conditioning. In data not illustrated in this figure, platelet FVIII conferred survival following tail-clip challenge in contrast to the FVIIInull mice in which this challenge was uniformly fatal. *P < .001. (Used with permission, with full details provided in J Clin Invest. 2006;116:1974-1982.)

FVIII in plasma and platelets in 2bF8-transgenic mice. Transgenic mice were developed with the cDNA for B domain-deleted FVIII placed under the control of the integrin α-IIb promoter and bred onto the murine FVIIInull background. These transgenic mice (2bF8) only expressed FVIII in megakaryocytes and stored FVIII together with VWF in platelets. (A) Plasma FVIII was measured and was present in wild-type (WT), but was absent in plasma from either FVIIInull or 2bF8 transgenic (FVIIInull) mice. (B) Platelet FVIII was measured in murine platelets and was absent in wild-type and FVIIInull mice; but, in 2bF8 transgenic mice, platelet FVIII was present and was greater in homozygous transgenic mice (2bF8trans+/+) than in heterozygous (2bF8trans+/–) mice. To determine the effect of VWF on the expression of FVIII in platelets, the 2bF8 transgene was bred onto the double KO background (FVIIInull VWFnull). Platelet FVIII expression was reduced in the absence of VWF. Bone marrow transplantation (BMT) from a heterozygous 2bF8 mouse conferred similar expression levels when transplanted into FVIIInull mice following ablative bone marrow conditioning. In data not illustrated in this figure, platelet FVIII conferred survival following tail-clip challenge in contrast to the FVIIInull mice in which this challenge was uniformly fatal. *P < .001. (Used with permission, with full details provided in J Clin Invest. 2006;116:1974-1982.)

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