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Updated: Oct 13, 2026

Pan-myeloid Differentiation of Human Cord Blood Derived CD34+ Hematopoietic Stem and Progenitor Cells
Published on: August 9, 2019
Interleukin 6 receptor expression by human cord blood- or peripheral blood-derived primitive haematopoietic
H Minamiguchi1, N Yahata, T Kimura
1Department of Hygiene, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Insights
Cord blood (CB) and peripheral blood (PB) progenitors differ in interleukin-6 receptor (IL-6R) expression and maturity. CB progenitors are less mature and more potent than PB progenitors, irrespective of IL-6R.
Area of Science:
- Hematology
- Cell Biology
- Immunology
Background:
- Interleukin 6 receptor (IL-6R) plays a role in hematopoietic stem cell regulation.
- Understanding IL-6R expression in different progenitor sources is crucial for cell therapy.
Purpose of the Study:
- To investigate the significance of IL-6R expression on cord blood (CB) and peripheral blood (PB) derived primitive hematopoietic progenitors.
- To compare the maturity and proliferative potential of CB- and PB-derived progenitors based on IL-6R expression.
Main Methods:
- Flow cytometry was used to analyze IL-6R expression on CD34+ cells from CB and PB.
- Long-term culture-initiating cell (LTC-IC) and extended LTC-IC (ELTC-IC) assays were performed.
- Telomerase activity was measured in different progenitor populations.
Main Results:
- IL-6R was preferentially expressed on PB-derived myeloid progenitors, while CB progenitors showed multipotentiality regardless of IL-6R status.
- PB-derived CD34+ cells showed enrichment of IL-6R+ cells in LTC-IC populations, unlike CB-derived cells.
- CB-derived progenitors exhibited higher LTC-IC and ELTC-IC numbers and distinct telomerase activity patterns compared to PB-derived progenitors, indicating less maturity.
Conclusions:
- CB-derived primitive hematopoietic progenitors are less mature and possess greater potential than PB-derived progenitors.
- IL-6R expression has differential implications for CB- and PB-derived CD34+ cells.
- Telomerase activity correlates with the proliferative potential of primitive hematopoietic progenitors, aiding in overcoming replicative senescence.
Abstract:
The significance of interleukin 6 receptor (IL-6R) expression by cord blood (CB)- and peripheral blood (PB)-derived primitive haematopoietic progenitors was investigated. IL-6R was preferentially expressed by PB-derived myeloid progenitors. Most PB-derived erythroid bursts (BFU-E) and mixed colony-forming cells (CFU-Mix) did not express this receptor. However, CB-derived primitive progenitor cells possessed multipotentiality, irrespective of IL-6R expression. Interestingly, the long-term culture-initiating cell (LTC-IC) population was enriched in PB-derived CD34+ IL-6R+ cells, but the extended LTC-IC (ELTC-IC) population, which represents a less mature class of haematopoietic progenitors, seemed to be equally distributed in the IL-6R+ and IL-6R- cell populations. In contrast, the number of LTC-ICs and ELTC-ICs was similar in CB-derived CD34+ IL-6R+ or IL-6R- cells. It is noteworthy that the number of LTC-ICs and ELTC-ICs in CB-derived CD34+ cells was markedly higher than that in PB-derived CD34+ cells regardless of IL-6R expression. Telomerase activity was consistently lower in PB-derived CD34+ IL-6R- cells than in CD34+ IL-6R+ cells. In contrast, telomerase activity was similar in CB-derived CD34+ IL-6R+ or IL-6R- cells. The pattern of telomerase induction upon cytokine stimulation differed between CB- and PB-derived CD34+ IL-6R+ or IL-6R- cells. However, overall telomerase activity per dish was well correlated with the proliferative potential of both cell populations, suggesting that induction of telomerase plays an important role in the escape from replicative senescence of primitive haematopoietic progenitors. Collectively, these results suggest that CB-derived primitive progenitors are less mature than PB-derived progenitors and that the expression of IL-6R by primitive haematopoietic progenitors may have different implications for PB- and CB-derived CD34+ cells.
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