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Updated: Aug 21, 2026

Isolation of Blood-vessel-derived Multipotent Precursors from Human Skeletal Muscle
Published on: August 21, 2014
Endothelial cells within embryonic skeletal muscles: a potential source of myogenic progenitors
Fabien Le Grand1, Gwenola Auda-Boucher, Dmitri Levitsky
1CNRS UMR 6204, Faculté des Sciences et des Techniques, 44322 Nantes Cedex 3, France.
Insights
Embryonic muscle endothelial cells, marked by CD34 and Flk1, can differentiate into skeletal muscle cells. These cells, when transplanted, restore dystrophin expression in mdx mouse muscles.
Area of Science:
- Developmental biology
- Cell biology
- Stem cell research
Background:
- Identifying sources of myogenic progenitors is crucial for muscle regeneration therapies.
- Endothelial cells are increasingly recognized for their potential plasticity.
- The specific origin and potential of embryonic muscle endothelial cells remain largely unexplored.
Purpose of the Study:
- To investigate if endothelial cells within mouse embryonic muscles can serve as myogenic progenitors.
- To characterize the properties and myogenic potential of these cells.
Main Methods:
- Immunodetection of CD34 and Flk1 stem cell markers in developing mouse embryo muscles.
- Purification of CD34-positive cells using magnetic-bead selection.
- Fluorescence-activated cell sorting (FACS) for cell characterization.
- In vitro differentiation assays and in vivo transplantation into mdx mouse models.
Main Results:
- CD34 and Flk1 markers were restricted to vessel-associated endothelial cells in embryonic muscles.
- Purified CD34+/Flk1+ cells differentiated into both endothelial cells and skeletal myofibers in vitro.
- Transplanted cells dispersed, fused with host myofibers, and restored dystrophin expression in mdx mouse muscles.
Conclusions:
- Embryonic muscle endothelial cells possess myogenic potential and can differentiate into skeletal myofibers.
- These cells are a promising candidate for cell-based therapies in muscular dystrophies.
- Their myogenic capacity may stem from their somitic origin.
Abstract:
We investigated whether the vessel-associated or endothelial cells within mouse embryo muscles can be a source of myogenic progenitors. Immunodetection of the stem cell surface markers, CD34 and Flk1, which are known to characterize the endothelial lineage, was done throughout the course of embryo muscle development. Both markers appeared to be restricted to the vessel-associated cells. On the basis of CD34 labeling, the reactive cells were purified by magnetic-bead selection from the limb muscles of 17-dpc desmin+/-LacZ mouse embryos and characterized by fluorescence-activated cell sorting. The cells in the selected CD34(+) population appeared to be approximately 95% positive for Flk1, but usually negative for CD45. We demonstrated that in vitro the CD34(+)/Flk1(+) population differentiated into endothelial cells and skeletal myofibers. When transplanted into mdx mouse muscle, this population displayed a high propensity to disperse within the recipient muscle, fuse with the host myofibers, and restore dystrophin expression. The marked ability of the embryonic muscle endothelial cells to activate myogenic program could be related to their somitic origin.
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