Abstract
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.
Crown Copyright © 2012. Published by Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cardiovascular System
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Cell Differentiation
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Cell Lineage*
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Endothelial Cells / cytology*
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Endothelial Cells / metabolism
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Endothelium, Vascular / cytology
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Endothelium, Vascular / metabolism
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Gene Expression Regulation, Developmental
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Heart / embryology
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LIM-Homeodomain Proteins / genetics*
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LIM-Homeodomain Proteins / metabolism
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Mice
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Mice, Inbred Strains
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Myocardium / metabolism
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Neuropeptides / genetics
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Neuropeptides / metabolism
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Stem Cells / cytology
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Stem Cells / metabolism
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Transcription Factors / genetics*
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Transcription Factors / metabolism
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rac GTP-Binding Proteins / genetics
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rac GTP-Binding Proteins / metabolism
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rac1 GTP-Binding Protein
Substances
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LIM-Homeodomain Proteins
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Neuropeptides
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Rac1 protein, mouse
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Transcription Factors
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insulin gene enhancer binding protein Isl-1
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rac GTP-Binding Proteins
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rac1 GTP-Binding Protein