Related Experiment Video
Updated: Aug 13, 2026

Pan-myeloid Differentiation of Human Cord Blood Derived CD34+ Hematopoietic Stem and Progenitor Cells
Published on: August 9, 2019
Diurnal variation of circulating human myeloid progenitor cells
D D Ross1, A Pollak, S A Akman
1Laboratory of Clinical Biochemistry, Baltimore Cancer Research Program, DCT, NCI, NIH, 655 West Baltimore Street, Baltimore, MD 21201, USA.
Insights
Human circulating myeloid progenitor cells (CFU(c)) show significant diurnal variation, peaking at 9 a.m. This finding highlights the importance of standardizing blood collection times for accurate CFU(c) measurements.
Area of Science:
- Hematology
- Chronobiology
- Cell Biology
Background:
- Circulating myeloid progenitor cells (CFU(c)) are crucial for hematopoiesis.
- Understanding diurnal variations in these cells is essential for accurate experimental design.
Purpose of the Study:
- To investigate diurnal variations in human peripheral blood CFU(c).
- To determine if specific myeloid progenitor subtypes exhibit circadian rhythms.
Main Methods:
- Peripheral venous blood samples were collected every 3 hours from nine healthy males.
- Mononuclear cells were isolated using Ficoll-Hypaque.
- CFU(c) content was quantified via soft agar cloning assay using human placental conditioned medium (HPCM).
Main Results:
- A statistically significant 24-hour cyclic variation in CFU(c) was observed, with a peak at 9 a.m. (P < 0.01).
- This diurnal variation was primarily attributed to eosinophilic colonies (CFU(eos)).
- Neutrophil/macrophage colonies (CFU(G,M)) showed a non-significant trend towards a 9 a.m. maximum.
Conclusions:
- Human peripheral blood CFU(c) exhibit significant diurnal variation.
- The time of blood collection must be standardized in experiments assessing peripheral blood CFU(c) to ensure reliable results.
Abstract:
We investigated whether human circulating myeloid progenitor cells (CFU(c)) exhibit diurnal variation. Peripheral venous blood samples were drawn every 3 h from each of the nine healthy male volunteers. Blood mononuclear cells were harvested by the Ficoll-Hypaque method. CFU(c) content of blood was determined by the soft agar cloning assay. Human placental conditioned medium (HPCM) was used as colony stimulating factor. We found a 24 h cyclic variation of colonies/10(5) mononuclear cells plated with a maximum at 9 a.m. (P < 0.01). Analysis of the colonies by in situ staining indicated that this variation could be attributed almost entirely to colonies composed of eosinophilic cells (representative of CFU(eos)). Neutrophil/macrophage colonies (representative of CFU(G,M)) exhibited a trend toward a 9 a.m. maximum, but this variation was not statistically significant. We conclude that time of blood collection should be standardized in experiments measuring human peripheral blood CFU(c).
More Related Videos
07:21Identification and Isolation of Oligopotent and Lineage-committed Myeloid Progenitors from Mouse Bone Marrow
Published on: July 29, 2018
09:05Generation of Large Numbers of Myeloid Progenitors and Dendritic Cell Precursors from Murine Bone Marrow Using a Novel Cell Sorting Strategy
Published on: August 10, 2018
Related Concept Videos
Differentiation of Common Myeloid Progenitor Cells
Hematopoiesis
Multipotency of Hematopoietic Stem Cells
Overview of Hematopoiesis
Developmental Phases of Hematopoiesis
Initially, HSCs are formed in the embryonic yolk sac, a critical site for early blood cell production. These stem cells subsequently migrate to other...
Production of Formed Elements
Most HSCs commit to...
Regulation of Hematopoietic Stem Cells