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Retroviral Overexpression of CXCR4 on Murine B-1a Cells and Adoptive Transfer for Targeted B-1a Cell Migration to the Bone Marrow and IgM Production
Published on: May 31, 2020
[Expressions of B-cell-specific monoclonal leukemia virus insert site 1 and human telomerase reverse transcriptase
Jianyun Ge1, Haibo Cai, Zheng Du
1State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, PR China.
Objective:
To investigate the relationship between the expressions of B-cell-specific monoclonal leukemia virus insert site 1 (Bmi1) and human telomerase reverse transcriptase (hTERT) genes and the proliferative capacity of stem cells.
Methods:
Cord blood CD34+ cells were cultured in IMDM medium containing fetal bovine serum, stem cell growth factor, thrombopoietin, and Fms-like tyrosine kinase 3 ligand during a 28-day ex vivo expansion process, while the expansion fold, specific growth rate, and the colony-forming efficiency were monitored. Then the Bmi1 and hTERT mRNA expressions in CD34+ cells were detected by fluorescence quantitative PCR, and the relations between the expressions and the cell proliferative capacity were analyzed.
Results:
CD34+ cells expanded (20.1 +/- 3.5) folds during the 28-day culture, while the proportion declined from 95.5% +/- 2.6% before culture to 2.1% +/- 0.4%. Both the specific growth rate and colony-forming efficiency of CD34+ cells declined significantly after 7 days, while the expression levels of Bmi1 and hTERT mRNA in CD34+ cells reached top at 7 days and declined gradually thereafter.
Conclusion:
The expressions of Bmi1 and hTERT genes may have a close relation to the proliferative capacity of CD34+ cells.

