Identification of MicroRNA Related to the CD34+ Cell Fraction of Cord Blood Stem Cells / 대한수혈학회지
Korean Journal of Blood Transfusion
; : 113-123, 2019.
Article
in En
| WPRIM
| ID: wpr-759594
Responsible library:
WPRO
ABSTRACT
BACKGROUND:
Cord blood (CB) is a reliable source of hematopoietic stem cells, and its utilization in stem cell transplantation is increasing continuously. The CD34+ cell count is arguably one of the most important parameters for evaluating the quality of a cord blood unit (CBU), but there is little evidence on the post-genetic modifications that can affect the CD34+ cell counts. In this study, the difference in the miRNA expression profiles between low and high CD34+ CBU was evaluated.METHODS:
Paired CB and maternal samples with low (0.9%) were selected for analysis. MicroRNA profiling was performed, and differentially expressed miRNA were identified. In addition, gene ontology analysis was conducted on the miRNA to elucidate the genes that could potentially affect the CD34+ cell count.RESULTS:
Ten miRNA were identified to show significantly different expression between the low and high CD34+ groups. Four of the 10 miRNA were hematopoiesis-related (miR-199a-5p, miR-22-5p, miR-140-5p, and miR-181b-5p). From a total of 119 associated genes, nine (CALCA, FARP2, FSHR, ITGAM, MELK, MLF1, PRG4, TREM2 and VCAM1) were associated with two or more of the aforementioned miRNA.CONCLUSION:
This is the first study that examined the difference in the miRNA expression profiles between high and low CD34+ CB cells and revealed the relevant genes associated with hematopoiesis. These results provide basic insight into the genetic processes involving hematopoietic stem cell proliferation.Key words
Full text:
1
Database:
WPRIM
Main subject:
Stem Cells
/
Hematopoietic Stem Cells
/
Cell Count
/
MicroRNAs
/
Stem Cell Transplantation
/
Genetic Phenomena
/
Fetal Blood
/
Gene Ontology
/
Hematopoiesis
Type of study:
Diagnostic_studies
Language:
En
Journal:
Korean Journal of Blood Transfusion
Year:
2019
Document type:
Article