Abstract
The transcription factor SCL/tal-1 is essential for blood cell development. Though it is also expressed in vascular endothelium, SCL has been considered dispensable for vessel formation. Through transgenic rescue of hematopoietic defects of SCL-/- embryos and analysis of chimeras generated with SCL-/- ES cells tagged with a transgene expressed in vascular endothelial cells, we show that SCL is essential for angiogenic remodeling of the yolk sac capillary network into complex vitelline vessels. These findings establish a role for SCL in embryonic angiogenesis and argue for critical functions in both embryonic blood and vascular cells, the descendents of the presumptive hemangioblast.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Basic Helix-Loop-Helix Transcription Factors
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Cell Division
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DNA-Binding Proteins / genetics*
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Endothelium, Vascular / cytology
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Endothelium, Vascular / embryology*
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Hematopoiesis / genetics
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Mice
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Mice, Transgenic
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Models, Cardiovascular
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Neovascularization, Physiologic / genetics*
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Proteins / genetics
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Proto-Oncogene Proteins*
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RNA, Untranslated
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Receptor Protein-Tyrosine Kinases / metabolism
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Receptor, TIE-2
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Recombinant Fusion Proteins
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T-Cell Acute Lymphocytic Leukemia Protein 1
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Transcription Factors / genetics*
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Vitelline Membrane / blood supply
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Yolk Sac / blood supply
Substances
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Basic Helix-Loop-Helix Transcription Factors
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DNA-Binding Proteins
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Gt(ROSA)26Sor non-coding RNA, mouse
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Proteins
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Proto-Oncogene Proteins
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RNA, Untranslated
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Recombinant Fusion Proteins
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T-Cell Acute Lymphocytic Leukemia Protein 1
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Tal1 protein, mouse
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Transcription Factors
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Receptor Protein-Tyrosine Kinases
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Receptor, TIE-2