Figure 1.
Figure 1. Increased adhesion of murine HS/HE RBCs to thrombospondin (TSP) and laminin (LM). Washed RBCs from control (WBB6F1-+/+ and -sph/+; CcS3/Dem-+/+ and -sphDem/+), elevated reticulocyte control (WBB6F1 Hi-ret), and mutant (severe HS: WBB6F1-sph/sph, -sph2BC/sph2BC, and -sphJ/sphJ; severe HE: CcS3/Dem-sphDem/sphDem) mice were perfused through flow chambers previously coated (2 μg/cm2) with human TSP (A) or human LM (B) at a wall shear stress of 1 dyne/cm2. Adherent RBCs per unit area were counted by direct microscopic visualization as described in “Materials and methods.” Group/genotype is listed on x-axis just below bars; numbers of measurements per group are indicated in parentheses below genotype/group. Strain background for each group is indicated between horizontal arrows. Adherent RBCs/mm2 are depicted as mean ± SEM. *P < .001 versus +/+ values.

Increased adhesion of murine HS/HE RBCs to thrombospondin (TSP) and laminin (LM). Washed RBCs from control (WBB6F1-+/+ and -sph/+; CcS3/Dem-+/+ and -sphDem/+), elevated reticulocyte control (WBB6F1 Hi-ret), and mutant (severe HS: WBB6F1-sph/sph, -sph2BC/sph2BC, and -sphJ/sphJ; severe HE: CcS3/Dem-sphDem/sphDem) mice were perfused through flow chambers previously coated (2 μg/cm2) with human TSP (A) or human LM (B) at a wall shear stress of 1 dyne/cm2. Adherent RBCs per unit area were counted by direct microscopic visualization as described in “Materials and methods.” Group/genotype is listed on x-axis just below bars; numbers of measurements per group are indicated in parentheses below genotype/group. Strain background for each group is indicated between horizontal arrows. Adherent RBCs/mm2 are depicted as mean ± SEM. *P < .001 versus +/+ values.

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