Figure 4
Altered response to chemically induced anemia in Lyn+/up adult mice. (A) Lyn+/up mice respond the same as control animals to PHZ treatment induced splenomegaly. Spleen wet weight of Lyn+/up and Lyn+/+ adult mice (12-15 weeks) at 0, 3, and 5 days after PHZ treatment (n > 6, *P < .05). (B) Lyn+/up hematocrits respond the same as control animals after PHZ induced red blood cell lysis. Analysis of the hematocrit in adult Lyn+/up and Lyn+/+ mice (12-15 weeks) at 0, 3, and 5 days after PHZ treatment (n > 6, *P < .05). (C) Extramedullary early erythroid progenitor (BFU-E) dynamics after PHZ treatment is similar in Lyn+/up and control mice. Early erythroid colony assays (BFU-E) of spleens in Lyn+/+ and Lyn+/up adult mice (12-15 weeks) (n = 6, *P < .05). (D) Extramedullary late erythroid progenitor (CFU-E) dynamics after PHZ treatment is elevated in Lyn+/up compared with control mice. Late erythroid colony assays (CFU-E) of spleens in Lyn+/+ and Lyn+/up adult mice (12-15 weeks) (n = 6, *P < .05). (E) Elevated maturing erythroid cells in the spleen of Lyn+/up adult mice 3 days after PHZ treatment. Representative flow cytometric analysis of spleen cells from Lyn+/+ and Lyn+/up mice (12-15 weeks) at 3 days after PHZ treatment using anti-CD71 and anti-Ter119 and enumeration of the indicated erythroid subsets (R0, R1, R2, R3, R4; n > 6, *P < .05).49 (F) Elevated maturing erythroid cells in the spleen of Lyn+/up adult mice 5 days after PHZ treatment. Representative flow cytometric analysis of spleen cells from Lyn+/+ and Lyn+/up mice (12-15 weeks) at 5 days after PHZ treatment using anti-CD71 and anti-Ter119 and enumeration as in E (n > 6, *P < .05).

Altered response to chemically induced anemia in Lyn+/up adult mice. (A) Lyn+/up mice respond the same as control animals to PHZ treatment induced splenomegaly. Spleen wet weight of Lyn+/up and Lyn+/+ adult mice (12-15 weeks) at 0, 3, and 5 days after PHZ treatment (n > 6, *P < .05). (B) Lyn+/up hematocrits respond the same as control animals after PHZ induced red blood cell lysis. Analysis of the hematocrit in adult Lyn+/up and Lyn+/+ mice (12-15 weeks) at 0, 3, and 5 days after PHZ treatment (n > 6, *P < .05). (C) Extramedullary early erythroid progenitor (BFU-E) dynamics after PHZ treatment is similar in Lyn+/up and control mice. Early erythroid colony assays (BFU-E) of spleens in Lyn+/+ and Lyn+/up adult mice (12-15 weeks) (n = 6, *P < .05). (D) Extramedullary late erythroid progenitor (CFU-E) dynamics after PHZ treatment is elevated in Lyn+/up compared with control mice. Late erythroid colony assays (CFU-E) of spleens in Lyn+/+ and Lyn+/up adult mice (12-15 weeks) (n = 6, *P < .05). (E) Elevated maturing erythroid cells in the spleen of Lyn+/up adult mice 3 days after PHZ treatment. Representative flow cytometric analysis of spleen cells from Lyn+/+ and Lyn+/up mice (12-15 weeks) at 3 days after PHZ treatment using anti-CD71 and anti-Ter119 and enumeration of the indicated erythroid subsets (R0, R1, R2, R3, R4; n > 6, *P < .05).49  (F) Elevated maturing erythroid cells in the spleen of Lyn+/up adult mice 5 days after PHZ treatment. Representative flow cytometric analysis of spleen cells from Lyn+/+ and Lyn+/up mice (12-15 weeks) at 5 days after PHZ treatment using anti-CD71 and anti-Ter119 and enumeration as in E (n > 6, *P < .05).

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