Abstract
Background
Umbilical cord blood (UCB) has improved into an attractive and alternative source
of allogeneic hematopoietic stem cells (all-HSCs) in clinics and, research for three
decades. Recently, it has been shown that the limited cell dose of, this valuable
source can be enhanced by the ex vivo expansion of cells in many, ways. We evaluated
the expression of the Gata transcription factors family and FOG-1, in expanded and
differentiated cord blood-derived CD34 + hematopoietic stem cells to, megakaryocytes
lineage., Methods: Separated mononuclear cells were cultured in DMEM complete medium.,
Harvested cells as a mesenchymal stem cell at 85 % confluency were cultured with,
trypsin/EDTA and in 24-well plates. The characteristic analyses of isolated UCB- MSCs,
were done by flow cytometry and adipogenic, chondrogenic, and osteogenic, differentiation
assays. MACS purified UCB-CD34 + hematopoietic cells cultivated and, differentiated
to megakaryocyte progenitor cells in the presence of cytokine cocktail, with UCB-MSCs.
Then, the GATA1, GATA2, GATA3, and FOG-1 genes expression, after differentiation to
megakaryocyte progenitor cells were performed by quantitative, real-time polymerase
chain reaction (PCR)., Results: In this study, the results of real-time-PCR showed
that the fold change, expression of GATA-1, FOG-1, and GATA-2 genes after co-culturing
with UCB-MSCs, significantly increased to 7.3, 4.7, and 3.3-fold in comparison with
control groups;respectively., Conclusion: UCB-MSCs can increase the expansion and
differentiation of UCBCD34 + , to megakaryocyte progenitor cells through upregulation
of GATA-1, GATA-2, and FOG-1 gene expression.
Keywords
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Article info
Publication history
Published online: June 06, 2022
Accepted:
June 3,
2022
Received in revised form:
May 26,
2022
Received:
November 29,
2021
Identification
Copyright
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