Publication | Open Access
Mesenchymal Stem Cells Derived from CD133‐Positive Cells in Mobilized Peripheral Blood and Cord Blood: Proliferation, Oct4 Expression, and Plasticity
437
Citations
37
References
2005
Year
Adult Stem CellPlastic AdhesionBiomedical EngineeringStem Cell MigrationStem Cell BiologyRegenerative MedicineMobilized Peripheral BloodStem Cell MobilizationBone MarrowStem Cell TraffickingStem CellsMesenchymal Stem CellCell BiologyDevelopmental BiologyStem Cell ResearchStem-cell TherapyCd133‐positive CellsMedicineOct4 ExpressionExtracellular Matrix
The study evaluates mobilized peripheral blood and umbilical cord blood as mesenchymal stem cell sources relative to bone marrow. MSCs were isolated by plastic adhesion (with or without 5 % BM‑MSC conditioned medium) and by selecting CD133‑positive cells, then characterized by mesenchymal marker expression and absence of hematopoietic markers. CD133‑positive cells from MPB and UCB yielded a homogeneous, highly proliferative MSC population that expresses Oct4 and can differentiate into adipocytes, osteocytes, chondrocytes, and neuronal/glial cells, indicating their potential clinical utility.
In this study, we used a common procedure to assess the potential of mobilized peripheral blood (MPB) and umbilical cord blood (UCB) as sources of mesenchymal stem cells (MSCs) in comparison with bone marrow (BM). We tested three methods: plastic adhesion supplemented with 5% of BM-MSC conditioned medium, unsupplemented plastic adhesion, and selection of CD133-positive cells. MSCs derived from MPB or UCB are identified by their positive expression of mesenchymal (SH2, SH3) and negative expression of hematopoietic markers (CD14, CD34, CD45, HLA-DR). We observed that the CD133-positive cell fraction contains more MSCs with high proliferative potential. Placed in appropriate conditions, these cells proved their capacity to differentiate into adipocytes, osteocytes, chondrocytes, and neuronal/glial cells. MPB- and UCB-MSCs express Oct4, a transcriptional binding factor present in undifferentiated cells with high proliferative capacity. The selection of CD133-positive cells enabled us to obtain a homogeneous population of MSCs from UCB and MPB. These sources may have a major clinical importance thanks to their easy accessibility.
| Year | Citations | |
|---|---|---|
Page 1
Page 1