Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2048226 | FEBS Letters | 2012 | 5 Pages |
The cardiovascular system consists of many cell types with distinct embryonic origins. Cells from an Islet1 (Isl1)-expressing progenitor population make a substantial contribution to the developing heart. We reasoned that cells derived from Isl1-expressing progenitors might contribute more widely to the cardiovascular system. We show that cells derived from an Isl1-expressing progenitor lineage make a wide contribution to the systemic vasculature and that embryos conditionally deficient for Rac1 within this cell population develop defects in the non-cardiac vasculature. These data define new roles for Isl1 in the developing embryo and demonstrate a contribution of Isl1-expressing progenitors to vascular endothelium in vivo.
► Isl1-expressing progenitor cells contribute to the non-cardiac vasculature. ► Isl1-expressing precursors give rise to endothelial derivatives in vivo. ► Deletion of Rac1 in Isl1+ cells results in failure of blood-lymph separation. ► Implications for conditional knock out studies in which Isl1Cre line has been used.