Figure 1.
Figure 1. Hematologic status of C3H/HeJwan homozygotes. (A) A C3H/HeJwan/wan newborn with a wild-type (+/+) littermate. Note the extreme pallor of the wan homozygote. (B) RBC volume and hemoglobin concentration histograms of whole blood from normal (+/+) and wan/wan (-/-) newborn mice. Significant populations of small (left panels) and dehydrated (right panels) RBCs are present in mutant blood compared with controls. (C) RBC counts are decreased in wan/wan fetuses compared with normal littermates. The differences are significant (*P < .001) by fetal day 18 and at birth. (D-E) Wright-stained peripheral blood smear from a newborn C3H+/+ mouse (D) and a mutant C3Hwan/wan mouse (E). Many RBC fragments (arrowheads) and membrane projections (arrows) are evident in mutant blood smears. Bar = 10 μM. (F-H) Scanning electron photomicrographs of normal (F) and mutant (G-H) RBCs. Mutant RBCs are predominantly spherocytic (G) with frequent membrane projections (H). Bar = 1 μM.

Hematologic status of C3H/HeJwan homozygotes. (A) A C3H/HeJwan/wan newborn with a wild-type (+/+) littermate. Note the extreme pallor of the wan homozygote. (B) RBC volume and hemoglobin concentration histograms of whole blood from normal (+/+) and wan/wan (-/-) newborn mice. Significant populations of small (left panels) and dehydrated (right panels) RBCs are present in mutant blood compared with controls. (C) RBC counts are decreased in wan/wan fetuses compared with normal littermates. The differences are significant (*P < .001) by fetal day 18 and at birth. (D-E) Wright-stained peripheral blood smear from a newborn C3H+/+ mouse (D) and a mutant C3Hwan/wan mouse (E). Many RBC fragments (arrowheads) and membrane projections (arrows) are evident in mutant blood smears. Bar = 10 μM. (F-H) Scanning electron photomicrographs of normal (F) and mutant (G-H) RBCs. Mutant RBCs are predominantly spherocytic (G) with frequent membrane projections (H). Bar = 1 μM.

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