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Updated: Apr 15, 2026

Purification, Expansion, and Flow Cytometry-Based Phenotyping of Mouse Derived Bone Marrow Mesenchymal Stem Cells
Published on: July 11, 2025
BMP2 repression and optimized culture conditions promote human bone marrow-derived mesenchymal stem cell isolation
Alasdair Gawain Kay1, Tina Patricia Dale, Khondoker Mehedi Akram
1Institute for Science & Technology in Medicine, Guy Hilton Research Centre, Keele University, Stoke-on-Trent, Staffordshire, ST4 7QB, UK.
Aim:
Human mesenchymal stem cells (hMSC) are multipotent progenitor cells. We propose the optimization of hMSC isolation and recovery using the application of a controlled hypoxic environment.
Materials & Methods:
We evaluated oxygen, glucose and serum in the recovery of hMSC from bone marrow (BMhMSC). Colony forming units-fibroblastic, cell numbers, tri-lineage differentiation, immunofluorescence and microarray were used to confirm and characterize BMhMSC.
Results:
In an optimized (2% O(2), 4.5 g/l glucose and 5% serum) environment both colony forming units-fibroblastic (p = 0.01) and cell numbers (p = 0.0001) were enhanced over standard conditions. Transcriptional analysis identified differential expression of bone morphogenetic protein 2 (BMP2) and, putatively, chemokine (C-X-C motif) receptor 2 (CXCR2) signaling pathways.
Conclusion:
We have detailed a potential milestone in the process of refinement of the BMhMSC isolation process.

