Fig. 3
- ID
- ZDB-FIG-091215-66
- Publication
- Lee et al., 2009 - Notch Signaling Functions as a Cell-Fate Switch between the Endothelial and Hematopoietic Lineages
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Reduced Notch Activity Causes an Increase of Endothelial Cells at the Expense of Hematopoietic Cells (A) Transverse sections of 18 hpf DMSO- or DAPT-treated embryos, visualized for TOPRO (white), kdrl:mCherry (red), and gata1:GFP (green). DAPT-treated embryos exhibited a concomitant gain of endothelial cells and loss of hematopoietic cells. (B) Transverse sections of 20 hpf DMSO- or DAPT-treated phenotypic bloodless (bds) mutant embryos, visualized for TOPRO (white), kdrl:GFP (green), and phalloidin (red). (C) Quantification of the number of endothelial nuclei per focal plane in DMSO-treated bds (n = 22), DAPT-treated bds (n = 20), and DAPT-treated wild-type sibling (n = 24) embryos. DAPT treatment in embryos lacking primitive hematopoietic cells (bds + DAPT) did not result in a change in the number of endothelial cells, suggesting that the ectopic endothelial cells observed in DAPT-treated wild-type embryos might have originated from cells that normally produce hematopoietic cells. |
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Stage: | 14-19 somites |