Figure 2
Figure 2. Altered adult erythropoiesis in TRα−/− mice. (A) Hematocrit level of 10-week-old TRα+/+ (n = 32), TRβ−/− (n = 28), and TRα−/− (n = 38) mice. (B) Spleen weight of TRα+/+ (+/+), TRα−/− (−/−), and TRα−/− “poor responder” (−/−*) mice 3 days after phenylhydrazine treatment (n = 6). Spleen weights before treatment were 100 to 120 mg. (C) Hematocrit level of mice taken 3 days after phenylhydrazine treatment (n = 6). (D) Enumeration of hemoglobin-positive (Hb+, arrow) and proerythroblasts (blast, arrowhead) in the spleens of phenylhydrazine-treated mice (n = 3). (E) Percentage of circulating reticulocytes (arrow) and erythrocytes (arrowhead) from mice 3 days after phenylhydrazine treatment (n = 3). (F) Total erythroid progenitors (BFU-Es and CFU-Es) in the spleens of TRα+/+ (+/+) and TRα−/− (−/−) mice 3 days after phenylhydrazine treatment (n = 3). (G) Morphology of erythroblasts from TRα+/+ (+/+) and TRα−/− (−/−) cultured for 3 days ex vivo (n = 3). (H) Flow cytometric analysis of spleen cells from TRα+/+ (+/+) and TRα−/−“poor responders” (−/−*) stained with CD71 and Ter119 (n = 4). Means (± SD) are shown. Statistically significant (2-way ANOVA) differences are indicated (*P ≤ .05; **P ≤ .01).

Altered adult erythropoiesis in TRα−/− mice. (A) Hematocrit level of 10-week-old TRα+/+ (n = 32), TRβ−/− (n = 28), and TRα−/− (n = 38) mice. (B) Spleen weight of TRα+/+ (+/+), TRα−/− (−/−), and TRα−/− “poor responder” (−/−*) mice 3 days after phenylhydrazine treatment (n = 6). Spleen weights before treatment were 100 to 120 mg. (C) Hematocrit level of mice taken 3 days after phenylhydrazine treatment (n = 6). (D) Enumeration of hemoglobin-positive (Hb+, arrow) and proerythroblasts (blast, arrowhead) in the spleens of phenylhydrazine-treated mice (n = 3). (E) Percentage of circulating reticulocytes (arrow) and erythrocytes (arrowhead) from mice 3 days after phenylhydrazine treatment (n = 3). (F) Total erythroid progenitors (BFU-Es and CFU-Es) in the spleens of TRα+/+ (+/+) and TRα−/− (−/−) mice 3 days after phenylhydrazine treatment (n = 3). (G) Morphology of erythroblasts from TRα+/+ (+/+) and TRα−/− (−/−) cultured for 3 days ex vivo (n = 3). (H) Flow cytometric analysis of spleen cells from TRα+/+ (+/+) and TRα−/−“poor responders” (−/−*) stained with CD71 and Ter119 (n = 4). Means (± SD) are shown. Statistically significant (2-way ANOVA) differences are indicated (*P ≤ .05; **P ≤ .01).

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