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Updated: Mar 16, 2026

Isolation of Blood-vessel-derived Multipotent Precursors from Human Skeletal Muscle
Published on: August 21, 2014
Mesenchymal Stem Cells and Endothelial Cells: A Common Ancestor?
Yousof Gheisari1, Naser Ahmadbeigi2
11)SABZ Biomedicals Research Center, Tehran, Iran. 2)Liver and Pancreatobiliary Diseases Research Center, Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran.
Early human bone marrow mesenchymal stem cell (BM-MSC) cultures reveal multinuclear cells expressing CD31. These cells may contribute to blood vessel formation, suggesting a novel role for MSC ancestors in angiogenesis.
Area of Science:
- Stem Cell Biology
- Vascular Biology
- Cellular Differentiation
Background:
- Bone marrow mesenchymal stem cells (BM-MSCs) are typically characterized as nonhematopoietic and nonendothelial in vitro.
- The in vivo identity and early developmental pathways of ex vivo expanded BM-MSCs remain largely unknown.
- Understanding the initial stages of BM-MSC culture is crucial for elucidating their potential roles in tissue regeneration and vascularization.
Purpose of the Study:
- To investigate the cellular morphology and marker expression of human BM-MSCs during the initial days of culture.
- To explore the potential of early BM-MSC cultures to contribute to vascular structures.
- To identify novel cell populations within BM-MSC cultures that may inform their in vivo function.
Main Methods:
- Culturing human bone marrow mesenchymal stem cells (BM-MSCs) under standard laboratory conditions.
- Microscopic observation of cellular morphology, including multinuclearity and tube-like structure formation.
- Immunophenotypic analysis using flow cytometry to assess the expression of specific cell surface markers (CD31, CD54, CD106, CD144).
Main Results:
- Large multinuclear cells positive for CD31 were observed at the beginning of human BM-MSC cultures.
- These multinuclear cells were occasionally seen forming tube-like structures.
- Subsequent differentiation yielded mononuclear cells meeting BM-MSC criteria, negative for CD31 but positive for endothelial markers CD54, CD106, and CD144.
Conclusions:
- Primitive multinuclear cells in early BM-MSC cultures express CD31 and may be involved in vascular development.
- These findings suggest that BM-MSC precursors could directly participate in angiogenesis.
- Further research is warranted to elucidate the precise role of these early cellular events in vascular system formation.
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