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      Macrophage colony-stimulating factor (M-CSF), as well as granulocyte colony-stimulating factor (G-CSF), accelerates neovascularization.

      Stem Cells (Dayton, Ohio)
      Animals, Bone Marrow Cells, drug effects, metabolism, Bone Marrow Transplantation, Cell Differentiation, Cell Proliferation, Endothelium, chemistry, Granulocyte Colony-Stimulating Factor, pharmacology, Green Fluorescent Proteins, genetics, H-2 Antigens, analysis, Hindlimb, blood supply, pathology, Ischemia, physiopathology, Macrophage Colony-Stimulating Factor, Mesenchymal Stromal Cells, cytology, Mice, Mice, Inbred C3H, Mice, Inbred C57BL, Mice, Transgenic, Muscle, Skeletal, Neovascularization, Physiologic, Regional Blood Flow, Vascular Endothelial Growth Factor A

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          Abstract

          It has been reported that bone marrow cells (BMCs) differentiate into endothelial cells of blood vessels, and that granulocyte colony-stimulating factor (G-CSF) mobilizes progenitors in the BMCs to the peripheral blood, while macrophage colony-stimulating factor (M-CSF) augments the production of monocytes. We examined whether M-CSF augments the differentiation of BMCs into endothelial cells of blood vessels using a hindlimb-ischemic model. Either G-CSF or M-CSF, or both, was administered to the hindlimb-ischemic mice for 3 days. Both M-CSF and G-CSF augmented the differentiation of BMCs into endothelial cells of blood vessels through vascular endothelial cell growth factor (VEGF), resulting in early recovery of blood flow in the ischemic limbs.

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