2002BloodRequires access

Runx1 is essential for hematopoietic commitment at the hemangioblast stage of development in vitro

Georges Lacaud

Open publisher page 302 citations

Abstract

In this report we demonstrate a role for Runx1 (AML1)at the hemangioblast stage of hematopoietic and endothelial development in embryonic stem (ES) cell–derived embryoid bodies (EBs).Runx1 is expressed in EBs during the appearance of precursors with hemangioblast properties, the blast colony-forming cells (BL-CFCs). Cell sorting studies revealed that all BL-CFCs within EBs express Runx1. Runx1-deficient EBs consistently generate 10- to 20-fold fewer blast colonies than wild-type controls and display a complete block in definitive hematopoiesis. Despite this defect, Runx1−/−EBs and yolk sacs from mutant embryos generate normal numbers of primitive erythroid precursors. These observations clearly demonstrate that Runx1 functions early in hematopoietic development, and they support the interpretation that the primitive erythroid lineage is established early by a subset of BL-CFCs that develop in aRunx1-independent fashion. Subjects: Hematopoiesis and Stem Cells Topics: basic local alignment search tool, chlorofluorocarbons, developmental stages, embryo, endothelium, hemangioblasts, yolk sac, cell separation, erythroid progenitor cells, hematopoiesis

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What this paper is about

In this report we demonstrate a role for Runx1 (AML1)at the hemangioblast stage of hematopoietic and endothelial development in embryonic stem (ES) cell–derived embryoid bodies (EBs).Runx1 is expressed in EBs during the appearance of precursors with hemangioblast properties, the blast colony-forming cells (BL-CFCs). Cell sorting studies revealed that all BL-CFCs within EBs express Runx1. Runx1-deficient EBs consistently generate 10- to 20-fold fewer blast colonies than wild-type controls and display a complete block in definitive hematopoiesis. Despite this defect, Runx1−/−EBs and yolk sacs from mutant embryos generate normal numbers of primitive erythroid precursors. These observations clearly demonstrate that Runx1 functions early in hematopoietic development, and they support the interpretation that the primitive erythroid lineage is established early by a subset of BL-CFCs that develop in aRunx1-independent fashion. Subjects: Hematopoiesis and Stem Cells Topics: basic local alignment search tool, chlorofluorocarbons, developmental stages, embryo, endothelium, hemangioblasts, yolk sac, cell separation, erythroid progenitor cells, hematopoiesis

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Available abstract

In this report we demonstrate a role for Runx1 (AML1)at the hemangioblast stage of hematopoietic and endothelial development in embryonic stem (ES) cell–derived embryoid bodies (EBs).Runx1 is expressed in EBs during the appearance of precursors with hemangioblast properties, the blast colony-forming cells (BL-CFCs). Cell sorting studies revealed that all BL-CFCs within EBs express Runx1. Runx1-deficient EBs consistently generate 10- to 20-fold fewer blast colonies than wild-type controls and display a complete block in definitive hematopoiesis. Despite this defect, Runx1−/−EBs and yolk sacs from mutant embryos generate normal numbers of primitive erythroid precursors. These observations clearly demonstrate that Runx1 functions early in hematopoietic development, and they support the interpretation that the primitive erythroid lineage is established early by a subset of BL-CFCs that develop in aRunx1-independent fashion. Subjects: Hematopoiesis and Stem Cells Topics: basic local alignment search tool, chlorofluorocarbons, developmental stages, embryo, endothelium, hemangioblasts, yolk sac, cell separation, erythroid progenitor cells, hematopoiesis

Key concepts: Hemangioblast, RUNX1, Embryoid body, Biology, Cell biology, Haematopoiesis, Yolk sac, Stem cell

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