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Updated: Feb 25, 2026

Isolation and Characterization of Mesenchymal Stromal Cells from Human Umbilical Cord and Fetal Placenta
Published on: April 3, 2017
Villous Chorion: A Potential Source for Pluripotent-like Stromal Cells
Jaianand Kannaiyan1, Palaniyandi Muthukutty2, M D Tabish Iqbal2
1Department of Biotechnology, M.G.R College, Hosur, Tamil Nadu, India.
Mesenchymal stem cells (MSCs) from the villous chorion (VC) demonstrate multipotency and stemness. These VC-MSCs are a promising source for regenerative medicine due to their differentiation capabilities.
Area of Science:
- Stem cell biology
- Regenerative medicine
- Tissue engineering
Background:
- Multipotent stromal cells (MSCs) are crucial for regenerative medicine.
- Fetal sources are explored for MSC isolation and characterization.
- Understanding MSC differentiation potential is key for therapeutic applications.
Purpose of the Study:
- To isolate and expand mesenchymal stem or stromal cells (MSCs) from the villous chorion (VC).
- To compare the potency of VC-MSCs with other fetal-derived MSCs.
- To assess the differentiation capabilities of VC-MSCs into all three germ layers.
Main Methods:
- Isolation of villous chorion-MSCs (VC-MSCs) from placenta obtained via C-section.
- Expansion of VC-MSCs up to the tenth passage.
- Phenotypic characterization using fluorescence-activated cell sorting (FACS).
- Assessment of differentiation into three germ layers via cytochemical staining.
Main Results:
- VC-MSCs yielded significant cell numbers, reaching 3.06-4.23 × 104 cells/cm2 by passage 10.
- Phenotypic analysis confirmed stemness, showing positive expression for CD73, CD90, CD105 and negative for CD79, CD34, CD45, HLA-DR.
- VC-MSCs differentiated into neural cells (ectoderm), hepatocytes (endoderm), and chondrocytes, adipocytes, osteogenic cells (mesoderm).
Conclusions:
- VC-MSCs exhibit characteristics similar to other adult stem cells.
- VC-derived MSCs are a viable source for clinical applications in regenerative medicine.
- The multipotent differentiation capacity of VC-MSCs supports their therapeutic potential.
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