Figure 3
Figure 3. Developmental mechanism and origin of dyserythropoiesis. (A-B) WISH analyses of αE1-globin in the indicated transgenic embryos at 75 hpf. The star, red arrow, and arrowheads indicate the increased number of erythrocytes expressing αE1-globin transcripts within the embryonic vasculature. (C-J) Time course of WISH analyses of scl in the transgenic embryos at indicated developmental stages. Red arrows and arrowheads indicate the increased scl+ HSPCs in the CHT and bilateral PDs. (K) Two-color WISH of EGFP (black color) and scl (red color) transcripts in the transgenic embryos at 32 hpf. (K-L) Fast red labeling of scl (RITC filter) is shown to the right. The red and black arrows indicate the colocalization of scl and EGFP.

Developmental mechanism and origin of dyserythropoiesis. (A-B) WISH analyses of αE1-globin in the indicated transgenic embryos at 75 hpf. The star, red arrow, and arrowheads indicate the increased number of erythrocytes expressing αE1-globin transcripts within the embryonic vasculature. (C-J) Time course of WISH analyses of scl in the transgenic embryos at indicated developmental stages. Red arrows and arrowheads indicate the increased scl+ HSPCs in the CHT and bilateral PDs. (K) Two-color WISH of EGFP (black color) and scl (red color) transcripts in the transgenic embryos at 32 hpf. (K-L) Fast red labeling of scl (RITC filter) is shown to the right. The red and black arrows indicate the colocalization of scl and EGFP.

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